Azinooximethers, processes and intermediate products for manufacturing same, and the uses thereof in combating harmful fungi and pests

The present invention relates to azinooxime ethers of the formula I ##STR2## where the variables have the following meanings:
X is NOCH.sub.3, CHOCH.sub.3 or CHCH.sub.3 ;
Y is O or NZ, Z being hydrogen or C.sub.1 -C.sub.4 -alkyl;
R.sup.1 is hydrogen or C.sub.1 -C.sub.4 -alkyl;
R.sup.2 is cyano, nitro, halogen, C.sub.1 -C.sub.4 -alkyl, trifluoromethyl or C.sub.1 -C.sub.4 -alkoxy;
m is 0, 1 or 2, it being possible for the radicals R.sup.2 to be different if m is 2;
R.sup.3 is hydrogen, cyano, alkyl, haloalkyl, alkoxy or cycloalkyl;
R.sup.4, R.sup.5, R.sup.6 independently of one another are: hydrogen or unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, heterocyclyl, aryl or heteroaryl,
and their salts.
The invention additionally relates to processes and intermediates for preparing these compounds and to compositions comprising them for controlling animal pests and harmful fungi.
Phenylacetic acid derivatives of type I having fungicidal and insecticidal action are disclosed in the following publication: WO-A 95/18789. The active compounds published there, however, are unsatisfactory with respect to their action.
It is an object of the present invention to provide novel compounds of this type having improved action against harmful fungi and pests.
We have found that this object is achieved by the azinooxime ethers I defined at the outset. We have additionally found processes and intermediates for their preparation and compositions comprising them for controlling animal pests and harmful fungi and their use for this purpose.
The compounds I are obtainable in various ways by processes known per se.
In principle, it is unimportant in the synthesis of the compounds I whether the group --C(X)--CO--YR.sup.1 or the group --CH.sub.2 ON.dbd.C(R.sup.3)--C(R.sup.4).dbd.N--N.dbd.C(R.sup.5)R.sup.6 is synthesized first.
The synthesis of the group --C(X)--CO--YR.sup.1 is disclosed, for example, in the following publications: EP-A 422 597, EP-A 463 488, EP-A 370 629, EP-A 460 575, EP-A 472 300, WO-A 90/07493, WO-A 92/13830, WO-A 92/18487, DE Appl. P 44 20 416.7.
1.1 In the synthesis of the group --CH.sub.2 ON.dbd.C(R.sup.3)--C(R.sup.4).dbd.N--N.dbd.C(R.sup.5)R.sup.6 a procedure is generally used in which a benzyl derivative of the formula II is reacted with a hydroxyimine of the formula III. ##STR3## L.sup.1 in the formula II is a nucleophilically replaceable leaving group, eg. halogen or a sulfonate group, preferably chlorine, bromine, iodine, mesylate, tosylate or triflate.
The reaction is carried out in a manner known per se in an inert organic solvent in the presence of a base, eg. sodium hydride, potassium hydroxide, potassium carbonate or triethylamine, according to the methods described in Houben-Weyl, 4th Edition, Vol. E 14b, p. 370 et seq. and Vol. 10/1, p. 1189 et seq.
1.2 The hydroxyimines III are obtained, for example, by reaction of a hydrazone V with a carbonyl compound of the formula VI. ##STR4## The reaction is carried out, if appropriate with acid catalysis, in a manner known per se in an inert organic solvent (cf. Bull. Soc. Chim. Fr. 713 (1968); Houben-Weyl, 4th Edition, Vol. X/2, page 104 et seq.).
The hydrazones V are known or can be prepared by methods known per se [cf. J. Med. Chem. 21 (1978), 623; J. Chem. Soc. 101 (1912), 2238; J. Org. Chem. 25 (1960), 313).
1.3 A further possibility for the preparation of the hydroxyimines III consists in reacting a carbonylhydroxyimino derivative IV with a hydrazone of the formula VII, as described in 1.2. ##STR5## 2. Alternatively, the compounds I can also be obtained by first reacting the benzyl derivative II with the carbonylhydroxyimino derivative IV to give a corresponding benzyloxime of the formula VIII, and then reacting VIII with a compound VII (see above) to give I. ##STR6## The reaction of IV with II is carried out similarly to the synthesis such as is described in 1.1. The reaction of VIII with VII is carried out similarly to the synthesis which is described in 1.2.
3.1 The synthesis of the compounds I is furthermore possible by reacting a compound of the formula VIII first with hydrazine hydrate to give the hydrazone of the formula IX and then reacting this with a carbonyl compound of the formula VI. ##STR7## The reactions are carried out similarly to the synthesis which is described in 1.2.
3.2 The synthesis of the derivatives IX is also possible by reacting a benzyl derivative of the formula II with a hydroxyimine of the formula V. ##STR8## L.sup.1 in the formula II is a nucleophilically replaceable leaving group, eg. halogen or a sulfonate group, preferably chlorine, bromine, iodine, mesylate, tosylate or triflate.
The reaction is carried out similarly to the synthesis which is described in 1.1.
4. In addition, the compounds I are obtained by first converting a compound III as in EP-A 493 711 using a lactone X into the corresponding benzoic acid XI and converting XI via the corresponding halides XII into the cyanocarboxylic acids XIII, which are converted by way of the Pinner reaction (Angew. Chem. 94, 1 (1982)) into the .alpha.-ketoesters XIV and, if desired, reacted further to give the .alpha.-ketoamides XV (cf. EP-A 348 766, DE-A 37 05 389, EP-A 178 826, DE-A 36 23 921, Houben-Weyl, 4th Edition, Vol. E5, pp. 941 et seq.) ##STR9##
The .alpha.-ketoesters XIV and the .alpha.-ketoamides XV can be converted into the compounds I according to customary processes (cf. EP-A 178 826, EP-A 348 766, DE-A 36 23 921, DE-A 37 05 389 and the literature cited at the outset).
Compounds I in which R.sup.1 is hydrogen are obtained according to this process by hydrolysis of the esters XIV and subsequent reaction to give I.
The compounds I in which Y is NZ can also be obtained from the esters (Y.dbd.O) by reaction with the appropriate amines HN(Z)R.sup.1.
The compounds II are disclosed in EP-A 513 580, EP-A 477 631, EP-A 463 488, EP-A 251 082, EP-A 400 417 and/or EP-A 585 751 or can be prepared by the methods described there.
On account of their C.dbd.C and C.dbd.N double bonds, the compounds I can be obtained during the preparation as E/Z isomer mixtures, which can be separated into the individual compounds in a customary manner, eg. by crystallization or chromatography.
If isomer mixtures are obtained during synthesis, in general, however, separation of the isomers is not absolutely necessary, as the individual isomers can partially be converted into one another during preparation for application or during application (eg. under the action of light, acid or base). Corresponding conversions can also take place after application, for example during the treatment of plants, in the treated plants or in the harmful fungus or animal pest to be controlled.
With regard to the C.dbd.X double bond, the E isomers of the compounds I are preferred with respect to their activity (configuration based on the --OCH.sub.3 or the --CH.sub.3 group in relation to the --COYR.sup.1 group).
With regard to the --C(R.sup.3).dbd.NOCH.sub.2 -- double bond, the cis isomers of the compounds I are preferred with respect to their activity (configuration based on the radical R.sup.3 in relation to the --OCH.sub.2 -- group).
Also part of the invention are the salts of the acid-stable compounds I, which contain basic centers, especially basic nitrogen atoms, in particular with mineral acids such as sulfuric acid and phosphoric acid or Lewis acids such as zinc chloride. Customarily, the nature of the salt does not matter here. Within the meaning of the invention, those salts are preferred which do not damage the plants, surfaces, materials or spaces to be kept free from harmful fungi or animal pests and do not adversely affect the action of the compounds I. Particularly important salts are those of the type suitable for agricultural purposes.
The salts of the compounds I are accessible in a manner known per se, especially by reacting the corresponding biphenylamides I with the acids mentioned in water or an inert organic solvent at from -80 to 120.degree. C., preferably 0 to 60.degree. C.
In the definitions of the compounds I given at the outset, collective terms were used which are generally representative of the following groups:
halogen: fluorine, chlorine, bromine and iodine;
alkyl: straight-chain or branched alkyl groups having 1 to 4, 6 or 10 carbon atoms, eg. C.sub.1 -C.sub.6 -alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl;
alkylamino: an amino group which carries a straight-chain or branched alkyl group having 1 to 6 carbon atoms as mentioned above;
dialkylamino: an amino group which carries two straight-chain or branched alkyl groups which are independent of one another and each have 1 to 6 carbon atoms as mentioned above;
alkylcarbonyl: straight-chain or branched alkyl groups having 1 to 10 carbon atoms, which are bonded to the structure via a carbonyl group (--CO--);
alkylsulfonyl: straight-chain or branched alkyl groups having 1 to 6 or 10 carbon atoms, which are bonded to the structure via a sulfonyl group (--SO.sub.2 --);
alkylsulfoxyl: straight-chain or branched alkyl groups having 1 to 6 carbon atoms, which are bonded to the structure via a sulfoxyl group (--S(.dbd.O)--);
alkylaminocarbonyl: alkylamino groups having 1 to 6 carbon atoms as mentioned above, which are bonded to the structure via a carbonyl group (--CO--);
dialkylaminocarbonyl: dialkylamino groups each having 1 to 6 carbon atoms per alkyl radical as mentioned above, which are bonded to the structure via a carbonyl group (--CO--);
alkylaminothiocarbonyl: alkylamino groups having 1 to 6 carbon atoms as mentioned above, which are bonded to the structure via a thiocarbonyl group (--CS--);
dialkylaminothiocarbonyl: dialkylamino groups each having 1 to 6 carbon atoms per alkyl radical as mentioned above, which are bonded to the structure via a thiocarbonyl group (--CS--);
haloalkyl: straight-chain or branched alkyl groups having 1 to 6 carbon atoms, it being possible in these groups for the hydrogen atoms to be partially or completely replaced by halogen atoms as mentioned above, eg. C.sub.1 -C.sub.2 -haloalkyl such as chloromethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl and pentafluoroethyl;
alkoxy: straight-chain or branched alkyl groups having 1 to 4 or 6 carbon atoms as mentioned above, which are bonded to the structure via an oxygen atom (--O--), eg. C.sub.1 -C.sub.6 -alkoxy such as methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy, 1,1-dimethylethoxy, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexyloxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy and 1-ethyl-2-methylpropoxy;
alkoxycarbonyl: straight-chain or branched alkyl groups having 1 to 6 carbon atoms, which are bonded to the structure via an oxycarbonyl group (--OC(.dbd.O)--);
alkylenedioxy: eg. C.sub.1 -C.sub.4 -alkylenedioxy: straight-chain or branched alkylene groups having 1 to 4 carbon atoms, which are bonded into the structure in two positions, each via an oxygen atom (--O--), or are bonded to the structure, such as methylenedioxy (--O--CH.sub.2 --O--) or 2,2-propylenedioxy (--O--C(CH.sub.3).sub.2 --O--);
haloalkoxy: straight-chain or branched alkyl groups having 1 to 6 carbon atoms, it being possible in these groups for the hydrogen atoms to be partially or completely replaced by halogen atoms as mentioned above, and these groups being bonded to the structure via an oxygen atom;
alkylthio: straight-chain or branched alkyl groups having 1 to 4 or 6 carbon atoms as mentioned above, which are bonded to the structure via a sulfur atom (--S--), eg. C.sub.1 -C.sub.6 -alkylthio such as methylthio, ethylthio, propylthio, 1-methylethylthio, butylthio, 1-methylpropylthio, 2-methylpropylthio, 1,1-dimethylethylthio, pentylthio, 1-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 2,2-dimethylpropylthio, 1-ethylpropylthio, hexylthio, 1,1-dimethylpropylthio, 1,2-dimethylpropylthio, 1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, 1,1-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio, 2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio, 1-ethylbutylthio, 2-ethylbutylthio, 1,1,2-trimethylpropylthio, 1,2,2-trimethylpropylthio, 1-ethyl-1-methylpropylthio and 1-ethyl-2-methylpropylthio;
cycloalkyl: monocyclic alkyl groups having 3 to 6 carbon ring members, eg. cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl;
alkenyl: straight-chain or branched alkenyl groups having 2 to 6 or 10 carbon atoms and a double bond in any desired position, eg. C.sub.2 -C.sub.6 -alkenyl such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl and 1-ethyl-2-methyl-2-propenyl;
alkenyloxy: straight-chain or branched alkenyl groups having 2 to 6 carbon atoms and a double bond in any desired position, which are bonded to the structure via an oxygen atom (--O--);
alkenylthio or alkenylamino: straight-chain or branched alkenyl groups having 2 to 6 carbon atoms and a double bond in any desired position, which (alkenylthio) are bonded to the structure via a sulfur atom or (alkenylamino) a nitrogen atom;
alkenylcarbonyl: straight-chain or branched alkenyl groups having 2 to 10 carbon atoms and a double bond in any desired position, which are bonded to the structure via a carbonyl group (--CO--);
alkynyl: straight-chain or branched alkynyl groups having 2 to 10 carbon atoms and a triple bond in any desired position, eg. C.sub.2 -C.sub.6 -alkynyl such as ethynyl, 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-4-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl and 1-ethyl-1-methyl-2-propynyl;
alkynyloxy or alkynylthio and alkynylamino: straight-chain or branched alkynyl groups having 2 to 6 carbon atoms and a triple bond in any desired position, which (alkynyloxy) are bonded to the structure via an oxygen atom or (alkynylthio) via a sulfur atom or (alkynylamino) via a nitrogen atom;
alkynylcarbonyl: straight-chain or branched alkynyl groups having 3 to 10 carbon atoms and a triple bond in any desired position, which are bonded to the structure via a carbonyl group (--CO--);
cycloalkenyl or cycloalkenyloxy, cycloalkenylthio and cycloalkenylamino: monocyclic alkenyl groups having 3 to 6 carbon ring members, which are bonded to the structure directly or (cycloalkenyloxy) via an oxygen atom or (cycloalkenylthio) a sulfur atom or (cycloalkenylamino) via a nitrogen atom, eg. cyclopropenyl, cyclobutenyl, cyclopentenyl or cyclohexenyl;
cycloalkoxy or cycloalkylthio and cycloalkylamino: monocyclic alkyl groups having 3 to 6 carbon ring members, which (cycloalkoxy) are bonded to the structure via an oxygen atom or (cycloalkylthio) a sulfur atom or (cycloalkylamino) via a nitrogen atom, eg. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;
heterocyclyl or heterocyclyloxy, heterocyclylthio and heterocyclylamino: three- to six-membered, saturated or partially unsaturated mono- or polycyclic heterocycles, which contain one to three heteroatoms selected from a group consisting of oxygen, nitrogen and sulfur, and which are bonded to the structure directly or (heterocyclyloxy) via an oxygen atom or (heterocyclylthio) via a sulfur atom or (heterocyclylamino) via a nitrogen atom, such as, for example, 2-tetrahydrofuranyl, oxiranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazoldinyl, 4-isoxazolidinyl, 5-isoxazolidinyl, 3-isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazolidinyl, 3-pyrazolidinyl, 4-pyrazolidinyl, 5-pyrazolidinyl, 2-oxazolidinyl, 4-oxazolidinyl, 5-oxazolidinyl, 2-thiazolidinyl, 4-thiazolidinyl, 5-thiazolidinyl, 2-imidazolidinyl, 4-imidazolidinyl, 1,2,4-oxadiazolidin-3-yl, 1,2,4-oxadiazolidin-5-yl, 1,2,4-thiadiazolidin-3-yl, 1,2,4-thiadiazolidin-5-yl, 1,2,4-triazolidin-3-yl, 1,3,4-oxadiazolidin-2-yl, 1,3,4-thiadiazolidin-2-yl, 1,3,4-triazolidin-2-yl, 2,3-dihydrofur-2-yl, 2,3-dihydrofur-3-yl, 2,3-dihydrofur-4-yl, 2,3-dihydrofur-5-yl, 2,5-dihydrofur-2-yl, 2,5-dihydrofur-3-yl, 2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,3-dihydrothien-4-yl, 2,3-dihydrothien-5-yl, 2,5-dihydrothien-2-yl, 2,5-dihydrothien-3-yl, 2,3-dihydropyrrol-2-yl, 2,3-dihydropyrrol-3-yl, 2,3-dihydropyrrol-4-yl, 2,3-dihydropyrrol-5-yl, 2,5-dihydropyrrol-2-yl, 2,5-dihydropyrrol-3-yl, 2,3-dihydroisoxazol-3-yl, 2,3-dihydroisoxazol-4-yl, 2,3-dihydroisoxazol-5-yl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, 4,5-dihydroisoxazol-5-yl, 2,5-dihydroisothiazol-3-yl, 2,5-dihydroisothiazol-4-yl, 2,5-dihydroisothiazol-5-yl, 2,3-dihydroisopyrazol-3-yl, 2,3-dihydroisopyrazol-4-yl, 2,3-dihydroisopyrazol-5-yl, 4,5-dihydroisopyrazol-3-yl, 4,5-dihydroisopyrazol-4-yl, 4,5-dihydroisopyrazol-5-yl, 2,5-dihydroisopyrazol-3-yl, 2,5-dihydroisopyrazol-4-yl, 2,5-dihydroisopyrazol-5-yl, 2,3-dihydrooxazol-3-yl, 2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 4,5-dihydrooxazol-3-yl, 4,5-dihydrooxazol-4-yl, 4,5-dihydrooxazol-5-yl, 2,5-dihydrooxazol-3-yl, 2,5-dihydrooxazol-4-yl, 2,5-dihydrooxazol-5-yl, 2,3-dihydrothiazol-2-yl, 2,3-dihydrothiazol-4-yl, 2,3-dihydrothiazol-5-yl, 4,5-dihydrothiazol-2-yl, 4,5-dihydrothiazol-4-yl, 4,5-dihydrothiazol-5-yl, 2,5-dihydrothiazol-2-yl, 2,5-dihydrothiazol-4-yl, 2,5-dihydrothiazol-5-yl, 2,3-dihydroimidazol-2-yl, 2,3-dihydroimidazol-4-yl, 2,3-dihydroimidazol-5-yl, 4,5-dihydroimidazol-2-yl, 4,5-dihydroimidazol-4-yl, 4,5-dihydroimidazol-5-yl, 2,5-dihydroimidazol-2-yl, 2,5-dihydroimidazol-4-yl, 2,5-dihydroimidazol-5-yl, 2-morpholinyl, 3-morpholinyl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 3-tetrahydropyridazinyl, 4-tetrahydropyridazinyl, 2-tetrahydropyrimidinyl, 4-tetrahydropyrimidinyl, 5-tetrahydropyrimidinyl, 2-tetrahydropyrazinyl, 1,3,5-tetrahydrotriazin-2-yl, 1,2,4-tetrahydrotriazin-3-yl, 1,3-dihydrooxazin-2-yl, 1,3-dithian-2-yl, 2-tetrahydropyranyl, 1,3-dioxolan-2-yl, 3,4,5,6-tetrahydropyridin-2-yl, 4H-1,3-thiazin-2-yl, 4H-3,1-benzothiazin-2-yl, 1,1-dioxo-2,3,4,5-tetrahydrothien-2-yl, 2H-1,4-benzothiazin-3-yl, 2H-1,4-benzoxazin-3-yl, 1,3-dihydrooxazin-2-yl, 1,3-dithian-2-yl;
aryl or aryloxy, arylthio, arylcarbonyl and arylsulfonyl: aromatic mono- or polycyclic hydrocarbon radicals which are bonded to the structure directly or (aryloxy) via an oxygen atom (--O--) or (arylthio) a sulfur atom (--S--), (arylcarbonyl) via a carbonyl group (--CO--) or (arylsulfonyl) via a sulfonyl group (--SO.sub.2 --), eg. phenyl, naphthyl and phenanthrenyl or phenoxy, naphthyloxy and phenanthrenyloxy and the corresponding carbonyl and sulfonyl radicals;
arylamino: aromatic mono- or polycyclic hydrocarbon radicals, which are bonded to the structure via a nitrogen atom;
heteroaryl or heteroaryloxy, heteroarylthio, heteroarylcarbonyl and hetarylsulfonyl: aromatic mono- or polycyclic radicals which, beside carbon ring members, can additionally contain one to four nitrogen atoms or one to three nitrogen atoms and an oxygen atom or a sulfur atom and which are bonded to the structure directly or (hetaryloxy) via an oxygen atom (--O--) or (hetarylthio) a sulfur atom (--S--), (hetarylcarbonyl) via a carbonyl group (--CO--) or (hetarylsulfonyl) via a sulfonyl group (--SO.sub.2 --), eg.
5-membered heteroaryl, containing one to three nitrogen atoms: 5-membered ring heteroaryl groups, which beside carbon atoms can contain one to three nitrogen atoms as ring members, eg. 2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-imidazolyl, 4-imidazolyl, 1,2,4-triazol-3-yl and 1,3,4-triazol-2-yl;
5-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and a sulfur or oxygen atom or an oxygen or a sulfur atom: 5-membered ring heteroaryl groups, which beside carbon atoms can contain one to four nitrogen atoms or one to three nitrogen atoms and a sulfur or oxygen atom or an oxygen or sulfur atom as ring members, eg. 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-imidazolyl, 4-imidazolyl, 1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl, 1,2,4-thiadiazol-3-yl, 1,2,4-thiadiazol-5-yl, 1,2,4-triazol-3-yl, 1,3,4-oxadiazol-2-yl, 1,3,4-thiadiazol-2-yl, 1,3,4-triazol-2-yl;
benzo-fused 5-membered heteroaryl, containing one to three nitrogen atoms or a nitrogen atom and/or an oxygen or sulfur atom: 5-membered ring heteroaryl groups, which beside carbon atoms can contain one to four nitrogen atoms or one to three nitrogen atoms and a sulfur or oxygen atom or an oxygen or a sulfur atom as ring members, and in which two adjacent carbon ring members or a nitrogen and an adjacent carbon ring member can be bridged by a buta-1,3-diene-1,4-diyl group;
5-membered heteroaryl bonded via nitrogen, containing one to four nitrogen atoms, or benzo-fused 5-membered heteroaryl bonded via nitrogen, containing one to three sulfur atoms: 5-membered ring heteroaryl groups, which beside carbon atoms can contain one to four nitrogen atoms or one to three nitrogen atoms as ring members, and in which two adjacent carbon ring members or a nitrogen and an adjacent carbon ring member can be bridged by a buta-1,3-diene-1,4-diyl group, these rings being bonded to the structure via one of the nitrogen ring members;
6-membered heteroaryl, containing one to three or one to four nitrogen atoms: 6-membered ring heteroaryl groups, which beside carbon atoms can contain one to three or one to four nitrogen atoms as ring members, eg. 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, 3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 2-pyrazinyl, 1,3,5-triazin-2-yl, 1,2,4-triazin-3-yl and 1,2,4,5-tetrazin-3-yl;
benzo-fused 6-membered heteroaryl, containing one to four nitrogen atoms: 6-membered ring heteroaryl groups in which two adjacent carbon ring members can be bridged by a buta-1,3-diene-1,4-diyl group, eg. quinoline, isoquinoline, quinazoline and quinoxaline,
or the corresponding oxy, thio, carbonyl or sulfonyl groups;
heteroarylamino: aromatic mono- or polycyclic radicals, which beside carbon ring members can additionally contain one to four nitrogen atoms or one to three nitrogen atoms and an oxygen or a sulfur atom and which are bonded to the structure via a nitrogen atom.
The statement "partially or completely halogenated" is intended to express that in the groups characterized in this way the hydrogen atoms can be partially or completely replaced by identical or different halogen atoms, as mentioned above.
The statement "unsubstituted or substituted" is intended to express that in the groups characterized in this way the hydrogen atoms can be partially or completely replaced by identical or different groups, for example those which are mentioned under the collective terms listed above.
With respect to their biological action, compounds of the formula I are preferred in which the variables have the following meanings:
X is NOCH.sub.3, CHOCH.sub.3 or CHCH.sub.3 ;
Y is O or NZ, Z being hydrogen or C.sub.1 -C.sub.4 -alkyl;
R.sup.1 is hydrogen or C.sub.1 -C.sub.4 -alkyl;
R.sup.2 is cyano, nitro, halogen, C.sub.1 -C.sub.4 -alkyl, trifluoromethyl or C.sub.1 -C.sub.4 -alkoxy;
m is 0, 1 or 2, it being possible for the radicals R.sup.2 to be different if m is 2;
R.sup.3 is hydrogen, cyano, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy or cyclopropyl;
R.sup.4, R.sup.5 and R.sup.6 independently of one another are:
hydrogen;
C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkynyl, it being possible for these radicals to be partially or completely halogenated and/or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -cycloalkyloxy, heterocyclyl, heterocyclyloxy, aryl, aryloxy, aryl-C.sub.1 -C.sub.4 -alkoxy, arylthio, aryl-C.sub.1 -C.sub.4 -alkylthio, heteroaryl, heteroaryloxy, heteroaryl-C.sub.1 -C.sub.4 -alkoxy, heteroarylthio and heteroaryl-C.sub.1 -C.sub.4 -alkylthio, it being possible for the cyclic groups in turn to be partially or completely halogenated and/or to carry one to three of the following substituents: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio, heteroaryl, heteroaryloxy, heteroarylthio, C.sub.3 -C.sub.6 -alkynyloxy, C.sub.1 -C.sub.4 -alkylenedioxy, which can be halogenated, and C(.dbd.NOR.sup.7)-A.sub.n -R.sup.8, A being oxygen, sulfur or nitrogen and the nitrogen carrying hydrogen or C.sub.1 -C.sub.6 -alkyl, n being 0 or 1, R.sup.7 being hydrogen or C.sub.1 -C.sub.6 -alkyl and R.sup.8 being hydrogen or C.sub.1 -C.sub.6 -alkyl;
C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -cycloalkenyl, heterocyclyl, it being possible for these radicals to be partially or completely halogenated and/or to carry one to three of the following groups: cyano, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.1 -C.sub.6 -alkoxy and C.sub.1 -C.sub.6 -alkylthio;
aryl or heteroaryl, it being possible for these radicals to be partially or completely halogenated and/or to carry one to three of the following groups: cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylsulfoxyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.1 -C.sub.6 -alkylaminocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminocarbonyl, C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, di-C.sub.1 -C.sub.6 -alkylaminothiocarbonyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, benzyl, benzyloxy, aryl, aryloxy, arylthio, heteroaryl, heteroaryloxy, heteroarylthio, C.sub.3 -C.sub.6 -alkynyloxy, C.sub.1 -C.sub.4 -alkylenedioxy, which can be halogenated, and C(.dbd.NOR.sup.7)-A.sub.n -R.sup.8,
A being oxygen, sulfur or nitrogen and the nitrogen carrying hydrogen or C.sub.1 -C.sub.6 -alkyl, n being 0 or 1, R.sup.7 being hydrogen or C.sub.1 -C.sub.6 -alkyl and R.sup.8 being hydrogen or C.sub.1 -C.sub.6 -alkyl
and it being possible for the cyclic groups in turn to be partially or completely halogenated and/or to carry one to three of the following substituents: cyano, nitro, hydroxyl, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylamino, di-C.sub.1 -C.sub.6 -alkylamino, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyloxy and C.sub.1 -C.sub.4 -alkylenedioxy, which can be halogenated;
R.sup.5 and R.sup.6, together with the carbon atom to which they are bonded, are an unsubstituted or substituted saturated or unsaturated carbocyclic or heterocyclic ring, if desired preferably substituted as follows: partially or completely halogenated and/or carrying one to three of the following groups: cyano, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.1 -C.sub.6 -alkoxy and C.sub.1 -C.sub.6 -alkylthio,
and their salts.
Furthermore, compounds of the formula I are preferred in which m is 0.
Equally, preferred compounds of the formula I are those in which R.sup.1 is methyl.
In addition, compounds I are preferred in which R.sup.3 is hydrogen, cyclopropyl, methyl, ethyl, 1-methylethyl, trifluoromethyl, cyano or methoxy.
Particularly preferred compounds I are those in which R.sup.3 is methyl.
In addition, compounds I are preferred in which R.sup.3 is trifluoromethyl.
Particularly preferred compounds I are also those in which R.sup.3 is methoxy.
In addition, compounds I are preferred in which R.sup.4 is unsubstituted or substituted C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -alkenyl or C.sub.2 -C.sub.6 -alkynyl.
Additionally, compounds I are preferred in which R.sup.4 is unsubstituted or substituted heterocyclyl or unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkenyl.
Particularly preferred compounds I are those in which R.sup.4 is C.sub.1 -C.sub.4 -alkyl.
Additionally, compounds I are preferred in which R.sup.4 is unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl.
In addition, compounds I are preferred in which R.sup.4 is unsubstituted or substituted aryl or hetaryl.
In addition, compounds I are preferred in which R.sup.4 is unsubst. or subst. pyridyl, pyrimidyl, pyrazinyl, pyridazinyl or triazinyl.
In addition, compounds I are preferred in which R.sup.4 is unsubst. or subst. furyl, thienyl or pyrrolyl.
In addition, compounds I are preferred in which R.sup.4 is unsubst. or subst. oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, pyrazolyl or imidazolyl.
In addition, compounds I are preferred in which R.sup.4 is unsubst. or subst. oxadiazolyl, thiadiazolyl or triazolyl.
Additionally, compounds I are preferred in which R.sup.4 is phenyl which is unsubstituted or carries one or two of the following groups: nitro, cyano, hydroxyl, amino, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.4 -alkylcarbonyl, di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.4 -alkylsulfonyl, C.sub.1 -C.sub.4 -alkoxycarbonyl, C.sub.1 -C.sub.4 -alkylaminocarbonyl, di-C.sub.1 -C.sub.4 -alkylaminocarbonyl, C.sub.1 -C.sub.4 -alkylthio, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyloxy and C.sub.1 -C.sub.4 -alkylenedioxy, which can be halogenated.
In addition, compounds I are preferred in which R.sup.5 is unsubstituted or substituted C.sub.1 -C.sub.6 -alkyl.
Additionally, compounds I are preferred in which R.sup.5 is methyl or ethyl.
In addition, compounds I are preferred in which R.sup.5 is hydrogen.
Additionally, compounds I are preferred in which R.sup.5 is unsubstituted or substituted C.sub.2 -C.sub.6 -alkenyl.
Furthermore, compounds I are preferred in which R.sup.5 is unsubstituted or substituted C.sub.2 -C.sub.6 -alkynyl.
Additionally, compounds I are preferred in which R.sup.5 is unsubstituted or substituted hetaryl.
In addition, compounds I are preferred in which R.sup.5 is unsubst. or subst. pyridyl, pyrimidyl, pyrazinyl, pyridazinyl or triazinyl.
In addition, compounds I are preferred in which R.sup.5 is unsubst. or subst. furyl, thienyl or pyrrolyl.
In addition, compounds I are preferred in which R.sup.5 is unsubst. or subst. oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, pyrazolyl or imidazolyl.
In addition, compounds I are preferred in which R.sup.5 is unsubst. or subst. aryl.
Additionally, compounds I are preferred in which R.sup.5 is phenyl which is unsubstituted or carries one or two of the following groups: nitro, cyano, hydroxyl, amino, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.4 -alkylcarbonyl, di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.4 -alkylsulfonyl, C.sub.1 -C.sub.4 -alkoxycarbonyl, C.sub.1 -C.sub.4 -alkylaminocarbonyl, di-C.sub.1 -C.sub.4 -alkylaminocarbonyl, C.sub.1 -C.sub.4 -alkylthio, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyloxy and C.sub.1 -C.sub.4 -alkylenedioxy, which can be halogenated.
In addition, compounds I are preferred in which R.sup.6 is unsubst. or subst. C.sub.1 -C.sub.6 -alkyl.
Additionally, compounds I are preferred in which R.sup.6 is methyl or ethyl.
In addition, compounds I are preferred in which R.sup.6 is hydrogen.
Additionally, compounds I are preferred in which R.sup.6 is unsubst. or subst. C.sub.2 -C.sub.6 -alkenyl.
Additionally, compounds I are preferred in which R.sup.6 is unsubst. or subst. C.sub.2 -C.sub.6 -alkynyl.
Additionally, compounds I are preferred in which R.sup.6 is unsubstituted or substituted hetaryl.
In addition, compounds I are preferred in which R.sup.6 is unsubst. or subst. pyridyl, pyrimidyl, pyrazinyl, pyridazinyl or triazinyl.
In addition, compounds I are preferred in which R.sup.6 is unsubst. or subst. furyl, thienyl or pyrrolyl.
In addition, compounds I are preferred in which R.sup.6 is unsubst. or subst. oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, pyrazolyl or imidazolyl.
In addition, compounds I are preferred in which R.sup.6 is unsubst. or subst. aryl.
Additionally, compounds I are preferred in which R.sup.6 is phenyl which is unsubstituted or carries one or two of the following groups: nitro, cyano, hydroxyl, amino, aminocarbonyl, aminothiocarbonyl, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.4 -alkylcarbonyl, di-C.sub.1 -C.sub.4 -alkylamino, C.sub.1 -C.sub.4 -alkylsulfonyl, C.sub.1 -C.sub.4 -alkoxycarbonyl, C.sub.1 -C.sub.4 -alkylaminocarbonyl, di-C.sub.1 -C.sub.4 -alkylaminocarbonyl, C.sub.1 -C.sub.4 -alkylthio, C.sub.2 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyloxy and C.sub.1 -C.sub.4 -alkylenedioxy, which can be halogenated.
In addition, compounds of the formula I are preferred in which X is NOCH.sub.3.
In addition, compounds of the formula I are preferred in which X is CHOCH.sub.3.
In addition, compounds of the formula I are preferred in which X is CHCH.sub.3.
In addition, compounds of the formula I are preferred in which Y is O.
Additionally, compounds of the formula I are preferred in which Y is NH.
In particular, the compounds compiled in the following tables are preferred with respect to their use.
The following tables (1 to 728) are based on the formulae I.1, I.2, I.3 and I.4, the double bonds marked by "E" having the E configuration: ##STR10##
Table 1
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =hydrogen;
R.sup.4 =in each case one line of Table A.
Table 2
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =hydrogen;
R.sup.4 =in each case one line of Table A.
Table 3
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =hydrogen;
R.sup.4 =in each case one line of Table A.
Table 4
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =hydrogen;
R.sup.4 =in each case one line of Table A.
Table 5
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =methyl;
R.sup.4 =in each case one line of Table A.
Table 6
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =methyl;
R.sup.4 =in each case one line of Table A.
Table 7
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =methyl;
R.sup.4 =in each case one line of Table A.
Table 8
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =methyl;
R.sup.4 =in each case one line of Table A.
Table 9
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 10
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 11
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 12
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 13
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 14
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 15
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 16
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 17
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 18
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 19
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 20
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 21
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 22
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 23
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 24
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 25
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =n-butyl;
R.sup.4 =in each case one line of Table A.
Table 26
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =n-butyl;
R.sup.4 =in each case one line of Table A.
Table 27
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =n-butyl;
R.sup.4 =in each case one line of Table A.
Table 28
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =n-butyl;
R.sup.4 =in each case one line of Table A.
Table 29
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =isobutyl;
R.sup.4 =in each case one line of Table A.
Table 30
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =isobutyl;
R.sup.4 =in each case one line of Table A.
Table 31
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =isobutyl;
R.sup.4 =in each case one line of Table A.
Table 32
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =isobutyl;
R.sup.4 =in each case one line of Table A.
Table 33
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =sec-butyl;
R.sup.4 =in each case one line of Table A.
Table 34
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =sec-butyl;
R.sup.4 =in each case one line of Table A.
Table 35
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =sec-butyl;
R.sup.4 =in each case one line of Table A.
Table 36
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =sec-butyl;
R.sup.4 =in each case one line of Table A.
Table 37
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =t-butyl;
R.sup.4 =in each case one line of Table A.
Table 38
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =t-butyl;
R.sup.4 =in each case one line of Table A.
Table 39
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =t-butyl;
R.sup.4 =in each case one line of Table A.
Table 40
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =t-butyl;
R.sup.4 =in each case one line of Table A.
Table 41
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 42
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 43
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 44
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 45
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =pentafluoroethyl;
R.sup.4 =in each case one line of Table A.
Table 46
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =pentafluoroethyl;
R.sup.4 =in each case one line of Table A.
Table 47
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =pentafluoroethyl;
R.sup.4 =in each case one line of Table A.
Table 48
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =pentafluoroethyl;
R.sup.4 =in each case one line of Table A.
Table 49
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =cyanomethyl;
R.sup.4 =in each case one line of Table A.
Table 50
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =cyanomethyl;
R.sup.4 =in each case one line of Table A.
Table 51
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =cyanomethyl;
R.sup.4 =in each case one line of Table A.
Table 52
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =cyanomethyl;
R.sup.4 =in each case one line of Table A.
Table 53
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =methoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 54
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =methoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 55
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =methoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 56
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =methoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 57
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =ethoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 58
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =ethoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 59
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =ethoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 60
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =ethoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 61
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =isopropoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 62
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =isopropoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 63
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =isopropoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 64
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =isopropoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 65
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =cyclopropylmethyl;
R.sup.4 =in each case one line of Table A.
Table 66
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =cyclopropylmethyl;
R.sup.4 =in each case one line of Table A.
Table 67
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =cyclopropylmethyl;
R.sup.4 =in each case one line of Table A.
Table 68
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =cyclopropylmethyl;
R.sup.4 =in each case one line of Table A.
Table 69
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 70
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 71
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 72
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 73
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 74
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 75
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 76
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 77
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =3-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 78
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =3-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 79
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =3-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 80
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =3-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 81
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 82
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 83
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 84
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 85
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-cyanophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 86
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-cyanophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 87
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-cyanophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 88
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-cyanophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 89
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-methylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 90
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-methylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 91
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-methylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 92
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-methylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 93
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =3-methoxyphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 94
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =3-methoxyphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 95
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =3-methoxyphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 96
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =3-methoxyphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 97
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-trifluoromethylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 98
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-trifluoromethylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 99
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-trifluoromethylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 100
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-trifluoromethylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 101
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-(3-nitrophenoxy)eth-1-yl;
R.sup.4 =in each case one line of Table A.
Table 102
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-(3-nitrophenoxy)eth-1-yl;
R.sup.4 =in each case one line of Table A.
Table 103
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-(3-nitrophenoxy)eth-1-yl;
R.sup.4 =in each case one line of Table A.
Table 104
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-(3-nitrophenoxy)eth-1-yl;
R.sup.4 =in each case one line of Table A.
Table 105
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 106
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 107
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 108
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 109
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-chloropyrimidin-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 110
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-chloropyrimidin-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 111
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-chloropyrimidin-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 112
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-chloropyrimidin-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 113
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylisoxazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 114
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylisoxazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 115
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylisoxazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 116
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylisoxazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 117
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =1-phenylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 118
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =1-phenylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 119
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =1-phenylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 120
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =1-phenylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 121
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =3-chloropyrid-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 122
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =3-chloropyrid-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 123
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =3-chloropyrid-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 124
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =3-chloropyrid-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 125
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-isopropyloxazol-4-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 126
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-isopropyloxazol-4-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 127
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-isopropyloxazol-4-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 128
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-isopropyloxazol-4-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 129
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =3-pyridazinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 130
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =3-pyridazinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 131
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =3-pyridazinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 132
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =3-pyridazinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 133
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylpyrimidin-2-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 134
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylpyrimidin-2-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 135
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylpyrimidin-2-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 136
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylpyrimidin-2-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 137
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 138
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 139
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 140
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 141
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =prop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 142
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =prop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 143
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =prop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 144
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =prop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 145
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =E-3-chloroprop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 146
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =E-3-chloroprop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 147
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =E-3-chloroprop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 148
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =E-3-chloroprop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 149
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =E-but-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 150
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =E-but-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 151
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =E-but-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 152
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =E-but-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 153
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 154
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 155
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 156
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 157
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =prop-2-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 158
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =prop-2-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 159
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =prop-2-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 160
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =prop-2-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 161
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 162
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 163
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 164
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 165
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =phenylethynyl;
R.sup.4 =in each case one line of Table A.
Table 166
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =phenylethynyl;
R.sup.4 =in each case one line of Table A.
Table 167
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =phenylethynyl;
R.sup.4 =in each case one line of Table A.
Table 168
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =phenylethynyl;
R.sup.4 =in each case one line of Table A.
Table 169
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =oxiran-2-yl;
R.sup.4 =in each case one line of Table A.
Table 170
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =oxiran-2-yl;
R.sup.4 =in each case one line of Table A.
Table 171
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =oxiran-2-yl;
R.sup.4 =in each case one line of Table A.
Table 172
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =oxiran-2-yl;
R.sup.4 =in each case one line of Table A.
Table 173
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =1,1-dichlorocyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 174
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =1,1-dichlorocyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 175
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =1,1-dichlorocyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 176
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =1,1-dichlorocyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 177
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 178
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 179
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 180
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 181
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-naphthyl;
R.sup.4 =in each case one line of Table A.
Table 182
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-naphthyl;
R.sup.4 =in each case one line of Table A.
Table 183
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-naphthyl;
R.sup.4 =in each case one line of Table A.
Table 184
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-naphthyl;
R.sup.4 =in each case one line of Table A.
Table 185
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 186
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 187
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 188
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 189
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =3-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 190
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =3-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 191
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =3-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 192
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =3-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 193
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 194
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 195
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 196
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 197
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-nitrophenyl;
R.sup.4 =in each case one line of Table A.
Table 198
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-nitrophenyl;
R.sup.4 =in each case one line of Table A.
Table 199
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-nitrophenyl;
R.sup.4 =in each case one line of Table A.
Table 200
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-nitrophenyl;
R.sup.4 =in each case one line of Table A.
Table 201
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 202
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 203
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 204
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 205
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-methylphenyl;
R.sup.4 =in each case one line of Table A.
Table 206
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-methylphenyl;
R.sup.4 =in each case one line of Table A.
Table 207
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-methylphenyl;
R.sup.4 =in each case one line of Table A.
Table 208
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-methylphenyl;
R.sup.4 =in each case one line of Table A.
Table 209
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =3-tert-butylphenyl;
R.sup.4 =in each case one line of Table A.
Table 210
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =3-tert-butylphenyl;
R.sup.4 =in each case one line of Table A.
Table 211
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =3-tert-butylphenyl;
R.sup.4 =in each case one line of Table A.
Table 212
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =3-tert-butylphenyl;
R.sup.4 =in each case one line of Table A.
Table 213
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-trifluoromethylphenyl;
R.sup.4 =in each case one line of Table A.
Table 214
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-trifluoromethylphenyl;
R.sup.4 =in each case one line of Table A.
Table 215
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-trifluoromethylphenyl;
R.sup.4 =in each case one line of Table A.
Table 216
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-trifluoromethylphenyl;
R.sup.4 =in each case one line of Table A.
Table 217
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 218
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 219
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 220
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 221
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2,4-dichlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 222
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2,4-dichlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 223
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2,4-dichlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 224
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2,4-dichlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 225
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 226
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 227
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 228
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 229
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-pyridyl;
R.sup.4 =in each case one line of Table A.
Table 230
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-pyridyl;
R.sup.4 =in each case one line of Table A.
Table 231
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-pyridyl;
R.sup.4 =in each case one line of Table A.
Table 232
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-pyridyl;
R.sup.4 =in each case one line of Table A.
Table 233
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-chloropyridin-6-yl;
R.sup.4 =in each case one line of Table A.
Table 234
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-chloropyridin-6-yl;
R.sup.4 =in each case one line of Table A.
Table 235
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-chloropyridin-6-yl;
R.sup.4 =in each case one line of Table A.
Table 236
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-chloropyridin-6-yl;
R.sup.4 =in each case one line of Table A.
Table 237
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylpyrimidin-2-yl;
R.sup.4 =in each case one line of Table A.
Table 238
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylpyrimidin-2-yl;
R.sup.4 =in each case one line of Table A.
Table 239
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylpyrimidin-2-yl;
R.sup.4 =in each case one line of Table A.
Table 240
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =5-methylpyrimidin-2-yl;
R.sup.4 =in each case one line of Table A.
Table 241
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =2-chloropyridin-5-yl;
R.sup.4 =in each case one line of Table A.
Table 242
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =2-chloropyridin-5-yl;
R.sup.4 =in each case one line of Table A.
Table 243
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =2-chloropyridin-5-yl;
R.sup.4 =in each case one line of Table A.
Table 244
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =2-chloropyridin-5-yl;
R.sup.4 =in each case one line of Table A.
Table 245
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =5-cyanothien-2-yl;
R.sup.4 =in each case one line of Table A.
Table 246
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =5-cyanothien-2-yl;
R.sup.4 =in each case one line of Table A.
Table 247
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =5-cyanothien-2-yl;
R.sup.4 =in each case one line of Table A.
Table 248
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =5-cyanothien-2-yl;
R.sup.4 =in each case one line of Table A.
Table 249
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorooxazol-2-yl;
R.sup.4 =in each case one line of Table A.
Table 250
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorooxazol-2-yl;
R.sup.4 =in each case one line of Table A.
Table 251
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorooxazol-2-yl;
R.sup.4 =in each case one line of Table A.
Table 252
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =4-chlorooxazol-2-yl;
R.sup.4 =in each case one line of Table A.
Table 253
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =1-methylpyrazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 254
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =1-methylpyrazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 255
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =1-methylpyrazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 256
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =1-methylpyrazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 257
Compounds of the formula I.1, where
R.sup.6 =hydrogen;
R.sup.5 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 258
Compounds of the formula I.2, where
R.sup.6 =hydrogen;
R.sup.5 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 259
Compounds of the formula I.3, where
R.sup.6 =hydrogen;
R.sup.5 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 260
Compounds of the formula I.4, where
R.sup.6 =hydrogen;
R.sup.5 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 261
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =n-hexyl;
R.sup.4 =in each case one line of Table A.
Table 262
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =n-hexyl;
R.sup.4 =in each case one line of Table A.
Table 263
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =n-hexyl;
R.sup.4 =in each case one line of Table A.
Table 264
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =n-hexyl;
R.sup.4 =in each case one line of Table A.
Table 265
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =methyl;
R.sup.4 =in each case one line of Table A.
Table 266
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =methyl;
R.sup.4 =in each case one line of Table A.
Table 267
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =methyl;
R.sup.4 =in each case one line of Table A.
Table 268
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =methyl;
R.sup.4 =in each case one line of Table A.
Table 269
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 270
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 271
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 272
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 273
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 274
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 275
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 276
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 277
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 278
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 279
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 280
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 281
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 282
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 283
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 284
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 285
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =n-butyl;
R.sup.4 =in each case one line of Table A.
Table 286
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =n-butyl;
R.sup.4 =in each case one line of Table A.
Table 287
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =n-butyl;
R.sup.4 =in each case one line of Table A.
Table 288
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =n-butyl;
R.sup.4 =in each case one line of Table A.
Table 289
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =isobutyl;
R.sup.4 =in each case one line of Table A.
Table 290
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =isobutyl;
R.sup.4 =in each case one line of Table A.
Table 291
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =isobutyl;
R.sup.4 =in each case one line of Table A.
Table 292
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =isobutyl;
R.sup.4 =in each case one line of Table A.
Table 293
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =sec-butyl;
R.sup.4 =in each case one line of Table A.
Table 294
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =sec-butyl;
R.sup.4 =in each case one line of Table A.
Table 295
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =sec-butyl;
R.sup.4 =in each case one line of Table A.
Table 296
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =sec-butyl;
R.sup.4 =in each case one line of Table A.
Table 297
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 298
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 299
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 300
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 301
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 302
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 303
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 304
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 305
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =pentafluoroethyl;
R.sup.4 =in each case one line of Table A.
Table 306
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =pentafluoroethyl;
R.sup.4 =in each case one line of Table A.
Table 307
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =pentafluoroethyl;
R.sup.4 =in each case one line of Table A.
Table 308
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =pentafluoroethyl;
R.sup.4 =in each case one line of Table A.
Table 309
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =cyanomethyl;
R.sup.4 =in each case one line of Table A.
Table 310
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =cyanomethyl;
R.sup.4 =in each case one line of Table A.
Table 311
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =cyanomethyl;
R.sup.4 =in each case one line of Table A.
Table 312
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =cyanomethyl;
R.sup.4 =in each case one line of Table A.
Table 313
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =methoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 314
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =methoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 315
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =methoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 316
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =methoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 317
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =ethoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 318
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =ethoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 319
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =ethoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 320
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =ethoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 321
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =isopropoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 322
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =isopropoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 323
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =isopropoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 324
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =isopropoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 325
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =cyclopropylmethyl;
R.sup.4 =in each case one line of Table A.
Table 326
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =cyclopropylmethyl;
R.sup.4 =in each case one line of Table A.
Table 327
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =cyclopropylmethyl;
R.sup.4 =in each case one line of Table A.
Table 328
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =cyclopropylmethyl;
R.sup.4 =in each case one line of Table A.
Table 329
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 330
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 331
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 332
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 333
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 334
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 335
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 336
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 337
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =3-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 338
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =3-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 339
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =3-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 340
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =3-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 341
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 342
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 343
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 344
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-chlorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 345
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-cyanophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 346
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-cyanophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 347
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-cyanophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 348
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-cyanophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 349
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-methylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 350
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-methylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 351
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-methylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 352
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-methylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 353
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =3-methoxyphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 354
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =3-methoxyphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 355
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =3-methoxyphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 356
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =3-methoxyphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 357
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-trifluoromethylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 358
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-trifluoromethylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 359
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-trifluoromethylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 360
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-trifluoromethylphenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 361
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-(3-nitrophenoxy)eth-1-yl;
R.sup.4 =in each case one line of Table A.
Table 362
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-(3-nitrophenoxy)eth-1-yl;
R.sup.4 =in each case one line of Table A.
Table 363
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-(3-nitrophenoxy)eth-1-yl;
R.sup.4 =in each case one line of Table A.
Table 364
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-(3-nitrophenoxy)eth-1-yl;
R.sup.4 =in each case one line of Table A.
Table 365
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 366
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 367
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 368
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 369
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-chloropyrimidin-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 370
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-chloropyrimidin-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 371
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-chloropyrimidin-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 372
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-chloropyrimidin-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 373
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =5-methylisoxazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 374
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =5-methylisoxazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 375
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =5-methylisoxazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 376
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =5-methylisoxazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 377
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =1-phenylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 378
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =1-phenylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 379
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =1-phenylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 380
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =1-phenylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 381
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =3-chloropyrid-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 382
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =3-chloropyrid-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 383
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =3-chloropyrid-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 384
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =3-chloropyrid-6-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 385
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-isopropyloxazol-4-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 386
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-isopropyloxazol-4-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 387
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-isopropyloxazol-4-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 388
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-isopropyloxazol-4-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 389
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =3-pyridazinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 390
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =3-pyridazinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 391
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =3-pyridazinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 392
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =3-pyridazinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 393
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =5-methylpyrimidin-2-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 394
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =5-methylpyrimidin-2-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 395
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =5-methylpyrimidin-2-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 396
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =5-methylpyrimidin-2-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 397
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 398
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 399
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 400
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 401
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =prop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 402
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =prop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 403
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =prop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 404
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =prop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 405
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =E-3-chloroprop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 406
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =E-3-chloroprop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 407
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =E-3-chloroprop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 408
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =E-3-chloroprop-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 409
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =E-but-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 410
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =E-but-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 411
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =E-but-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 412
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =E-but-2-en-1-yl;
R.sup.4 =in each case one line of Table A.
Table 413
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 414
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 415
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 416
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 417
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =prop-2-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 418
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =prop-2-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 419
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =prop-2-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 420
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =prop-2-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 421
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 422
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 423
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 424
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 425
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =phenylethynyl;
R.sup.4 =in each case one line of Table A.
Table 426
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =phenylethynyl;
R.sup.4 =in each case one line of Table A.
Table 427
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =phenylethynyl;
R.sup.4 =in each case one line of Table A.
Table 428
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =phenylethynyl;
R.sup.4 =in each case one line of Table A.
Table 429
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =oxiran-2-yl;
R.sup.4 =in each case one line of Table A.
Table 430
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =oxiran-2-yl;
R.sup.4 =in each case one line of Table A.
Table 431
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =oxiran-2-yl;
R.sup.4 =in each case one line of Table A.
Table 432
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =oxiran-2-yl;
R.sup.4 =in each case one line of Table A.
Table 433
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =1,1-dichlorocyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 434
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =1,1-dichlorocyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 435
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =1,1-dichlorocyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 436
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =1,1-dichlorocyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 437
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 438
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 439
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 440
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 441
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-naphthyl;
R.sup.4 =in each case one line of Table A.
Table 442
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-naphthyl;
R.sup.4 =in each case one line of Table A.
Table 443
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-naphthyl;
R.sup.4 =in each case one line of Table A.
Table 444
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-naphthyl;
R.sup.4 =in each case one line of Table A.
Table 445
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 446
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 447
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 448
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 449
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =3-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 450
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =3-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 451
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =3-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 452
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =3-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 453
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 454
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 455
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 456
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 457
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-nitrophenyl;
R.sup.4 =in each case one line of Table A.
Table 458
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-nitrophenyl;
R.sup.4 =in each case one line of Table A.
Table 459
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-nitrophenyl;
R.sup.4 =in each case one line of Table A.
Table 460
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-nitrophenyl;
R.sup.4 =in each case one line of Table A.
Table 461
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 462
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 463
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 464
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 465
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-methylphenyl;
R.sup.4 =in each case one line of Table A.
Table 466
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-methylphenyl;
R.sup.4 =in each case one line of Table A.
Table 467
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-methylphenyl;
R.sup.4 =in each case one line of Table A.
Table 468
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-methylphenyl;
R.sup.4 =in each case one line of Table A.
Table 469
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =3-tert-butylphenyl;
R.sup.4 =in each case one line of Table A.
Table 470
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =3-tert-butylphenyl;
R.sup.4 =in each case one line of Table A.
Table 471
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =3-tert-butylphenyl;
R.sup.4 =in each case one line of Table A.
Table 472
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =3-tert-butylphenyl;
R.sup.4 =in each case one line of Table A.
Table 473
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-trifluoromethylphenyl;
R.sup.4 =in each case one line of Table A.
Table 474
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-trifluoromethylphenyl;
R.sup.4 =in each case one line of Table A.
Table 475
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-trifluoromethylphenyl;
R.sup.4 =in each case one line of Table A.
Table 476
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-trifluoromethylphenyl;
R.sup.4 =in each case one line of Table A.
Table 477
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 478
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 479
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 480
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 481
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2,4-dichlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 482
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2,4-dichlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 483
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2,4-dichlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 484
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2,4-dichlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 485
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 486
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 487
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 488
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 489
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-pyridyl;
R.sup.4 =in each case one line of Table A.
Table 490
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-pyridyl;
R.sup.4 =in each case one line of Table A.
Table 491
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-pyridyl;
R.sup.4 =in each case one line of Table A.
Table 492
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-pyridyl;
R.sup.4 =in each case one line of Table A.
Table 493
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-chloropyridin-6-yl;
R.sup.4 =in each case one line of Table A.
Table 494
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-chloropyridin-6-yl;
R.sup.4 =in each case one line of Table A.
Table 495
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-chloropyridin-6-yl;
R.sup.4 =in each case one line of Table A.
Table 496
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-chloropyridin-6-yl;
R.sup.4 =in each case one line of Table A.
Table 497
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =5-methylpyrimidin-2-yl;
R.sup.4 =in each case one line of Table A.
Table 498
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =5-methylpyrimidin-2-yl;
R.sup.4 =in each case one line of Table A.
Table 499
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =5-methylpyrimidin-2-yl;
R.sup.4 =in each case one line of Table A.
Table 500
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =5-methylpyrimidin-2-yl;
R.sup.4 =in each case one line of Table A.
Table 501
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =2-chloropyridin-5-yl;
R.sup.4 =in each case one line of Table A.
Table 502
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =2-chloropyridin-5-yl;
R.sup.4 =in each case one line of Table A.
Table 503
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =2-chloropyridin-5-yl;
R.sup.4 =in each case one line of Table A.
Table 504
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =2-chloropyridin-5-yl;
R.sup.4 =in each case one line of Table A.
Table 505
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =5-cyanothien-2-yl;
R.sup.4 =in each case one line of Table A.
Table 506
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =5-cyanothien-2-yl;
R.sup.4 =in each case one line of Table A.
Table 507
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =5-cyanothien-2-yl;
R.sup.4 =in each case one line of Table A.
Table 508
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =5-cyanothien-2-yl;
R.sup.4 =in each case one line of Table A.
Table 509
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =4-chlorooxazol-2-yl;
R.sup.4 =in each case one line of Table A.
Table 510
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =4-chlorooxazol-2-yl;
R.sup.4 =in each case one line of Table A.
Table 511
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =4-chlorooxazol-2-yl;
R.sup.4 =in each case one line of Table A.
Table 512
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =4-chlorooxazol-2-yl;
R.sup.4 =in each case one line of Table A.
Table 513
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =1-methoxypyrazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 514
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =1-methoxypyrazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 515
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =1-methoxypyrazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 516
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =1-methoxypyrazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 517
Compounds of the formula I.1, where
R.sup.6 =methyl;
R.sup.5 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 518
Compounds of the formula I.2, where
R.sup.6 =methyl;
R.sup.5 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 519
Compounds of the formula I.3, where
R.sup.6 =methyl;
R.sup.5 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 520
Compounds of the formula I.4, where
R.sup.6 =methyl;
R.sup.5 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl;
R.sup.4 =in each case one line of Table A.
Table 521
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 522
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 523
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 524
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =ethyl;
R.sup.4 =in each case one line of Table A.
Table 525
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 526
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 527
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 528
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 529
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 530
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 531
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 532
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 533
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 534
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 535
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 536
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 537
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 538
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 539
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 540
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 541
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 542
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 543
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 544
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 545
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 546
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 547
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 548
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 549
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 550
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 551
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 552
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 553
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =5-methylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 554
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =5-methylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 555
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =5-methylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 556
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =5-methylpyrazol-3-yloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 557
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 558
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 559
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 560
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 561
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 562
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 563
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 564
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 565
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 566
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 567
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 568
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 569
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 570
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 571
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 572
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 573
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 574
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 575
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 576
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 577
Compounds of the formula I.1, where
R.sup.6 =ethyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 578
Compounds of the formula I.2, where
R.sup.6 =ethyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 579
Compounds of the formula I.3, where
R.sup.6 =ethyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 580
Compounds of the formula I.4, where
R.sup.6 =ethyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 581
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 582
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 583
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 584
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 585
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 586
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 587
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 588
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =isopropyl;
R.sup.4 =in each case one line of Table A.
Table 589
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 590
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 591
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 592
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 593
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 594
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 595
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 596
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 597
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =4-fluorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 598
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =4-fluorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 599
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =4-fluorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 600
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =4-fluorophenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 601
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 602
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 603
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 604
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =2-pyridyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 605
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 606
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 607
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 608
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 609
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 610
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 611
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 612
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =prop-1-yn-1-yl;
R.sup.4 =in each case one line of Table A.
Table 613
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 614
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 615
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 616
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 617
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 618
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 619
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 620
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =3-cyanophenyl;
R.sup.4 =in each case one line of Table A.
Table 621
Compounds of the formula I.1, where
R.sup.6 =isopropyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 622
Compounds of the formula I.2, where
R.sup.6 =isopropyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 623
Compounds of the formula I.3, where
R.sup.6 =isopropyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 624
Compounds of the formula I.4, where
R.sup.6 =isopropyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 625
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 626
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 627
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 628
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =cyclopropyl;
R.sup.4 =in each case one line of Table A.
Table 629
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 630
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 631
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 632
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 633
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 634
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 635
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 636
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 637
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =2-pyridinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 638
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =2-pyridinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 639
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =2-pyridinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 640
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =2-pyridinyloxymethyl;
R.sup.4 =in each case one line of Table A.
Table 641
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 642
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 643
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 644
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =ethenyl;
R.sup.4 =in each case one line of Table A.
Table 645
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 646
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 647
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 648
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =ethynyl;
R.sup.4 =in each case one line of Table A.
Table 649
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 650
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 651
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 652
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 653
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 654
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 655
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 656
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 657
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 658
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 659
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 660
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 661
Compounds of the formula I.1, where
R.sup.6 =cyclopropyl;
R.sup.5 =2-methylpyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 662
Compounds of the formula I.2, where
R.sup.6 =cyclopropyl;
R.sup.5 =2-methylpyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 663
Compounds of the formula I.3, where
R.sup.6 =cyclopropyl;
R.sup.5 =2-methylpyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 664
Compounds of the formula I.4, where
R.sup.6 =cyclopropyl;
R.sup.5 =2-methylpyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 665
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 666
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 667
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 668
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =n-propyl;
R.sup.4 =in each case one line of Table A.
Table 669
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 670
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 671
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 672
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =tert-butyl;
R.sup.4 =in each case one line of Table A.
Table 673
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 674
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 675
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 676
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =trifluoromethyl;
R.sup.4 =in each case one line of Table A.
Table 677
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 678
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 679
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 680
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =phenoxymethyl;
R.sup.4 =in each case one line of Table A.
Table 681
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 682
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 683
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 684
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 685
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 686
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 687
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 688
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 689
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 690
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 691
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 692
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 693
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =3-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 694
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =3-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 695
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =3-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 696
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =3-methoxyphenyl;
R.sup.4 =in each case one line of Table A.
Table 697
Compounds of the formula I.1, where
R.sup.6 =trifluoromethyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 698
Compounds of the formula I.2, where
R.sup.6 =trifluoromethyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 699
Compounds of the formula I.3, where
R.sup.6 =trifluoromethyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 700
Compounds of the formula I.4, where
R.sup.6 =trifluoromethyl;
R.sup.5 =2-chloropyrid-6-yl;
R.sup.4 =in each case one line of Table A.
Table 701
Compounds of the formula I.1, where
R.sup.6 =phenyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 702
Compounds of the formula I.2, where
R.sup.6 =phenyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 703
Compounds of the formula I.3, where
R.sup.6 =phenyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 704
Compounds of the formula I.4, where
R.sup.6 =phenyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 705
Compounds of the formula I.1, where
R.sup.6 =phenyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 706
Compounds of the formula I.2, where
R.sup.6 =phenyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 707
Compounds of the formula I.3, where
R.sup.6 =phenyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 708
Compounds of the formula I.4, where
R.sup.6 =phenyl;
R.sup.5 =4-fluorophenyl;
R.sup.4 =in each case one line of Table A.
Table 709
Compounds of the formula I.1, where
R.sup.6 =methoxymethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 710
Compounds of the formula I.2, where
R.sup.6 =methoxymethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 711
Compounds of the formula I.3, where
R.sup.6 =methoxymethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 712
Compounds of the formula I.4, where
R.sup.6 =methoxymethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 713
Compounds of the formula I.1, where
R.sup.6 =methoxymethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 714
Compounds of the formula I.2, where
R.sup.6 =methoxymethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 715
Compounds of the formula I.3, where
R.sup.6 =methoxymethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 716
Compounds of the formula I.4, where
R.sup.6 =methoxymethyl;
R.sup.5 =4-chlorophenyl;
R.sup.4 =in each case one line of Table A.
Table 717
Compounds of the formula I.1, where
R.sup.6 =2-pyrimidinyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 718
Compounds of the formula I.2, where
R.sup.6 =2-pyrimidinyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 719
Compounds of the formula I.3, where
R.sup.6 =2-pyrimidinyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 720
Compounds of the formula I.4, where
R.sup.6 =2-pyrimidinyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 721
Compounds of the formula I.1, where
R.sup.6 =cyanomethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 722
Compounds of the formula I.2, where
R.sup.6 =cyanomethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 723
Compounds of the formula I.3, where
R.sup.6 =cyanomethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 724
Compounds of the formula I.4, where
R.sup.6 =cyanomethyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 725
Compounds of the formula I.1, where
R.sup.6 =n-propyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 726
Compounds of the formula I.2, where
R.sup.6 =n-propyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 727
Compounds of the formula I.3, where
R.sup.6 =n-propyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
Table 728
Compounds of the formula I.4, where
R.sup.6 =n-propyl;
R.sup.5 =phenyl;
R.sup.4 =in each case one line of Table A.
TABLE A______________________________________No. R.sup.4______________________________________1 H 2 CH.sub.3 3 C.sub.2 H.sub.5 4 n-C.sub.3 H.sub.7 5 i-C.sub.3 H.sub.7 6 cyclopropyl 7 n-C.sub.4 H.sub.9 8 s-C.sub.4 H.sub.9 9 i-C.sub.4 H.sub.9 10 t-C.sub.4 H.sub.9 11 n-C.sub.5 H.sub.11 12 i-C.sub.5 H.sub.11 13 neo-C.sub.5 H.sub.11 14 cyclopentyl 15 n-C.sub.6 H.sub.13 16 cyclohexyl 17 cyclobutyl 18 CH.sub.2 CH.sub.2 Cl 19 (CH.sub.2).sub.4 Cl 20 CH.sub.2 CN 21 CH.sub.2 CH.sub.2 CN 22 (CH.sub.2).sub.3 CN 23 (CH.sub.2).sub.4 CN 24 (CH.sub.2).sub.6 CN 25 cyclohexylmethyl 26 2-cyclohexyleth-1-yl 27 cyclopropylmethyl 28 2-cyclopropyleth-1-yl 29 2-methoxyeth-1-yl 30 2-ethoxyeth-1-yl 31 2-isopropoxyeth-1-yl 32 3-methoxyprop-1-yl 33 3-ethoxyprop-1-yl 34 3-isopropoxyprop-1-yl 35 4-methoxybut-1-yl 36 4-isopropoxybut-1-yl 37 prop-2-en-1-yl 38 but-2-en-1-yl 39 3-methylbut-2-en-1-yl 40 2-vinyloxyeth-1-yl 41 allyloxyeth-1-yl 42 2-trifluoromethoxyeth-1-yl 43 3-trifluoromethoxyprop-1-yl 44 4-difluoromethoxybut-1-yl 45 hydroxycarbonylmethyl 46 methoxycarbonylmethyl 47 aminocarbonylmethyl 48 N-methylaminocarbonylmethyl 49 N,N-dimethylaminocarbonylmethyl 50 2-hydroxycarbonyleth-1-yl 51 2-methoxycarbonyleth-1-yl 52 2-aminocarbonyleth-1-yl 53 2-N-methylaminocarbonyleth-1-yl 54 2-dimethylaminocarbonyleth-1-yl 55 2-aminoeth-1-yl 56 2-aminoprop-1-yl 57 4-aminobut-1-yl 58 3-dimethylaminoprop-1-yl 59 4-aminothiocarbonylbut-1-yl 60 E-3-chloroprop-2-en-1-yl 61 Z-3-chloroprop-2-en-1-yl 62 prop-2-yn-1-yl 63 but-2-yn-1-yl 64 but-3-yn-1-yl 65 3-chloroprop-2-yn-1-yl 66 6-aminocarbonylhex-1-yl 67 3-aminothiocarbonylprop-1-yl 68 2-aminothiocarbonyleth-1-yl 69 aminothiocarbonylmethyl 70 4-(N,N-dimethylamino)but-1-yl 71 2-(methylthio)eth-1-yl 72 2-(methylsulfonyl)eth-1-yl 73 4-(methylthio)prop-1-yl 74 4-(methylsulfonyl)prop-1-yl 75 benyzl 76 2-F-C.sub.6 H.sub.4 --CH.sub.2 77 3-F-C.sub.6 H.sub.4 --CH.sub.2 78 4-F-C.sub.6 H.sub.4 --CH.sub.2 79 2,3-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 80 2,4-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 81 2,5-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 82 2,6-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 83 3,4-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 84 3,5-F.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 85 2-Cl-C.sub.6 H.sub.4 --CH.sub.2 86 3-Cl-C.sub.6 H.sub.4 --CH.sub.2 87 4-Cl-C.sub.6 H.sub.4 --CH.sub.2 88 2,3-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 89 2,4-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 90 2,5-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 91 2,6-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 92 3,4-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 93 3,5-Cl.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 94 2,3,4-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 95 2,3,5-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 96 2,3,6-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 97 2,4,5-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 98 2,4,6-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 99 3,4,5-Cl.sub.3 --C.sub.6 H.sub.2 --CH.sub.2 100 2-Br--C.sub.6 H.sub.4 --CH.sub.2 101 3-Br--C.sub.6 H.sub.4 --CH.sub.2 102 4-Br--C.sub.6 H.sub.4 --CH.sub.2 103 2,3-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 104 2,4-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 105 2,5-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 106 2,6-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 107 3,4-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 108 3,5-Br.sub.2 --C.sub.6 H.sub.3 --CH.sub.2 109 2-F,3-Cl--C.sub.6 H.sub.3 --CH.sub.2 110 2-F,4-Cl--C.sub.6 H.sub.3 --CH.sub.2 111 2-F,5-Cl--C.sub.6 H.sub.3 --CH.sub.2 112 2-F,3-Br--C.sub.6 H.sub.3 --CH.sub.2 113 2-F, 4-Br--C.sub.6 H.sub.3 --CH.sub.2 114 2-F, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 115 2-Cl, 3-Br--C.sub.6 H.sub.3 --CH.sub.2 116 2-Cl, 4-Br--C.sub.6 H.sub.3 --CH.sub.2 117 2-Cl, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 118 3-F, 4-Cl--C.sub.6 H.sub.3 --CH.sub.2 119 3-F, 5-Cl--C.sub.6 H.sub.3 --CH.sub.2 120 3-F, 6-Cl--C.sub.6 H.sub.3 --CH.sub.2 121 3-F, 4-Br--C.sub.6 H.sub.3 --CH.sub.2 122 3-F, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 123 3-F, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 124 3-Cl, 4-Br--C.sub.6 H.sub.3 --CH.sub.2 125 3-Cl, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 126 3-Cl, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 127 4-F, 5-Cl--C.sub.6 H.sub.3 --CH.sub.2 128 4-F, 6-Cl--C.sub.6 H.sub.3 --CH.sub.2 129 4-F, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 130 4-F, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 131 4-Cl, 5-Br--C.sub.6 H.sub.3 --CH.sub.2 132 5-F, 6-Cl--C.sub.6 H.sub.3 --CH.sub.2 133 5-F, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 134 5-Cl, 6-Br--C.sub.6 H.sub.3 --CH.sub.2 135 3-Br, 4-Cl, 5-Br--C.sub.6 H.sub.2 --CH.sub.2 136 2-CN--C.sub.6 H.sub.4 --CH.sub.2 137 3-CN--C.sub.6 H.sub.4 --CH.sub.2 138 4-CN--C.sub.6 H.sub.4 --CH.sub.2 139 2-NO.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 140 3-NO.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 141 4-NO.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 142 2-CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 143 3-CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 144 4-CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 145 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 146 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 147 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 148 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 149 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 150 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 151 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 152 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 153 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 154 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 --CH.sub.2 155 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 --CH.sub.2 156 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 --CH.sub.2 157 2-cyclohexyl-C.sub.6 H.sub.4 --CH.sub.2 158 3-cyclohexyl-C.sub.6 H.sub.4 --CH.sub.2 159 4-cyclohexyl-C.sub.6 H.sub.4 --CH.sub.2 160 2-vinyl-C.sub.6 H.sub.4 --CH.sub.2 161 3-vinyl-C.sub.6 H.sub.4 --CH.sub.2 162 4-vinyl-C.sub.6 H.sub.4 --CH.sub.2 163 2-allyl-C.sub.6 H.sub.4 --CH.sub.2 164 3-allyl-C.sub.6 H.sub.4 --CH.sub.2 165 4-allyl-C.sub.6 H.sub.4 --CH.sub.2 166 2-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 167 3-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 168 4-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 169 3-CH.sub.3, 5-t-C.sub.4 H.sub.9 --C.sub.6 H.sub.3 --CH.sub.2 170 2-OH--C.sub.6 H.sub.4 --CH.sub.2 171 3-OH--C.sub.6 H.sub.4 --CH.sub.2 172 4-OH--C.sub.6 H.sub.4 --CH.sub.2 173 2-OCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 174 3-OCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 175 4-OCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 176 2,3-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 177 2,4-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 178 2,5-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 179 3,4-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 180 3,5-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 --CH.sub.2 181 3,4,5-(OCH.sub.3).sub.3 --C.sub.6 H.sub.2 --CH.sub.2 182 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 183 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 184 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 --CH.sub.2 185 2-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 186 3-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 187 4-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 188 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 189 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 190 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 --CH.sub.2 191 4-O-(n-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 --CH.sub.2 192 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 --CH.sub.2 193 4-O-(n-C.sub.6 H.sub.13) -C.sub.6 H.sub.4 --CH.sub.2 194 2-O-allyl-C.sub.6 H.sub.4 --CH.sub.2 195 3-O-allyl-C.sub.6 H.sub.4 --CH.sub.2 196 4-O-allyl-C.sub.6 H.sub.4 --CH.sub.2 197 2-CF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 198 3-CF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 199 4-CF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 200 2-acetyl-C.sub.6 H.sub.4 --CH.sub.2 201 3-acetyl-C.sub.6 H.sub.4 --CH.sub.2 202 4-acetyl-C.sub.6 H.sub.4 --CH.sub.2 203 2-methoxycarbonyl-C.sub.6 H.sub.4 --CH.sub.2 204 3-methoxycarbonyl-C.sub.6 H.sub.4 --CH.sub.2 205 4-methoxycarbonyl-C.sub.6 H.sub.4 --CH.sub.2 206 2-aminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 207 3-aminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 208 4-aminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 209 2-dimethylaminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 210 3-dimethylaminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 211 4-dimethylaminocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 212 2-(N-methylaminocarbonyl)-C.sub.6 H.sub.4 --CH.sub.2 213 3-(N-methylaminocarbonyl)-C.sub.6 H.sub.4 --CH.sub.2 214 4-(N-methylaminocarbonyl)-C.sub.6 H.sub.4 --CH.sub.2 215 2-H.sub.2 N--C.sub.6 H.sub.4 --CH.sub.2 216 3-H.sub.2 N--C.sub.6 H.sub.4 --CH.sub.2 217 4-H.sub.2 N--C.sub.6 H.sub.4 --CH.sub.2 218 2-aminothiocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 219 3-aminothiocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 220 4-aminothiocarbonyl-C.sub.6 H.sub.4 --CH.sub.2 221 2-methoxyiminomethyl-C.sub.6 H.sub.4 --CH.sub.2 222 3-methoxyiminomethyl-C.sub.6 H.sub.4 --CH.sub.2 223 4-methoxyiminomethyl-C.sub.6 H.sub.4 --CH.sub.2 224 3,4-methylenedioxy-C.sub.6 H.sub.3 --CH.sub.2 225 3,4-difluoromethylenedioxy-C.sub.6 H.sub.3 --CH.sub.2 226 2,3-methylenedioxy-C.sub.6 H.sub.3 --CH.sub.2 227 2-(1'-methoxyiminoeth-1'-yl)-C.sub.6 H.sub.4 --CH.sub.2 228 3-(1'-methoxyiminoeth-1'-yl)-C.sub.6 H.sub.4 --CH.sub.2 229 4-(1'-methoxyiminoeth-1'-yl)-C.sub.6 H.sub.4 --CH.sub.2 230 2-SCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 231 3-SCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 232 4-SCH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 233 2-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 234 3-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 235 4-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 236 2-OCF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 237 3-OCF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 238 4-OCF.sub.3 --C.sub.6 H.sub.4 --CH.sub.2 239 2-OCHF.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 240 3-OCHF.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 241 4-OCHF.sub.2 --C.sub.6 H.sub.4 --CH.sub.2 242 3-CF.sub.3, 4-OCF.sub.3 --C.sub.6 H.sub.3 --CH.sub.2 243 1-naphthyl-CH.sub.2 244 2-naphthyl-CH.sub.2 245 2-phenoxyeth-1-yl 246 2-(2'-chlorophenoxy)eth-1-yl 247 2-(3'-chlorophenoxy)eth-1-yl 248 2-(4'-chlorophenoxy)eth-1-yl 249 2-(3',5'-dichlorophenoxy)eth-1-yl 250 2-(2'-cyanophenoxy)eth-1-yl 251 2-(3'-cyanophenoxy)eth-1-yl 252 2-(4'-cyanophenoxy)eth-1-yl 253 2-(2'-methylphenoxy)eth-1-yl 254 2-(3'-methylphenoxy)eth-1-yl 255 2-(4'-methylphenoxy)eth-1-yl 256 2-(3'-t-butylphenoxy)eth-1-yl 257 2-(4'-t-butylphenoxy)eth-1-yl 258 2-(2'-nitrophenoxy)eth-1-yl 259 2-(3'-nitrophenoxy)eth-1-yl 260 2-(4'-nitrophenoxy)eth-1-yl 261 2-(2'-methoxyphenoxy)eth-1-yl 262 2-(3'-methoxyphenoxy)eth-1-yl 263 2-(4'-methoxyphenoxy)eth-1-yl 264 2-(2'-trifluoromethylphenoxy)eth-1-yl 265 2-(3'-trifluoromethylphenoxy)eth-1-yl 266 2-(4'-trifluoromethylphenoxy)eth-1-yl 267 2-(2'-acetylphenoxy)eth-1-yl 268 2-(3'-acetylphenoxy)eth-1-yl 269 2-(4'-acetylphenoxy)eth-1-yl 270 2-(2'-methoxycarbonyl)eth-1-yl 271 2-(3'-methoxycarbonyl)eth-1-yl 272 2-(4'-methoxycarbonyl)eth-1-yl 273 2-(2'-dimethylaminocarbonyl)eth-1-yl 274 2-(3'-dimethylaminocarbonyl)eth-1-yl 275 2-(4'-dimethylaminocarbonyl)eth-1-yl 276 2-(2'-aminothiocarbonyl)eth-1-yl 277 2-(3'-aminothiocarbonyl)eth-1-yl 278 2-(4'-aminothiocarbonyl)eth-1-yl 279 2-(2'-methylsulfonyl)eth-1-yl 280 2-(3'-methylsulfonyl)eth-1-yl 281 2-(4'-methylsulfonyl)eth-1-yl 282 3-phenoxyprop-1-yl 283 3-(2'-chlorophenoxy)prop-1-yl 284 3-(3'-chlorophenoxy)prop-1-yl 285 3-(4'-chlorophenoxy)prop-1-yl 286 3-(3',5'-dichlorophenoxy)prop-1-yl 287 3-(2'-cyanophenoxy)prop-1-yl 288 3-(3'-cyanophenoxy)prop-1-yl 289 3-(4'-cyanophenoxy)prop-1-yl 290 3-(2'-methylphenoxy)prop-1-yl 291 3-(3'-methylphenoxy)prop-1-yl 292 3-(4'-methylphenoxy)prop-1-yl 293 3-(2'-methoxyphenoxy)prop-1-yl 294 3-(3'-methoxyphenoxy)prop-1-yl 295 3-(4'-methoxyphenoxy)prop-1-yl 296 3-(2'-trifluoromethylphenoxy)prop-1-yl 297 3-(3'-trifluoromethylphenoxy)prop-1-yl 298 3-(4'-trifluoromethylphenoxy)prop-1-yl 299 4-phenoxybut-1-yl 300 2-phenyleth-1-yl 301 2-(2'-chlorophenyl)eth-1-yl 302 2-(3'-chlorophenyl)eth-1-yl 303 2-(4'-chlorophenyl)eth-1-yl 304 2-(3',5'-dichlorophenyl)eth-1-yl 305 2-(2'-cyanophenyl)eth-1-yl 306 2-(3'-cyanophenyl)eth-1-yl 307 2-(4'-cyanophenyl)eth-1-yl 308 2-(2'-methylphenyl)eth-1-yl 309 2-(3'-methylphenyl)eth-1-yl 310 2-(4'-methylphenyl)eth-1-yl 311 2-(2'-methoxyphenyl)eth-1-yl 312 2-(3'-methoxyphenyl)eth-1-yl 313 2-(4'-methoxyphenyl)eth-1-yl 314 2-(2'-trifluoromethylphenyl)eth-1-yl 315 2-(3'-trifluoromethylphenyl)eth-1-yl 316 2-(4'-trifluoromethylphenyl)eth-1-yl 317 3-phenylprop-1-yl 318 3-(2'-chlorophenyl)prop-1-yl 319 3-(3'-chlorophenyl)prop-1-yl 320 3-(4'-chlorophenyl)prop-1-yl 321 3-(2'-cyanophenyl)prop-1-yl 322 3-(3'-cyanophenyl)prop-1-yl 323 3-(4'-cyanophenyl)prop-1-yl 324 3-(2'-trifluoromethylphenyl)prop-1-yl 325 4-phenylbut-1-yl 326 4-(4'-chlorophenyl)but-1-yl 327 6-(4'-chlorophenyl)hex-1-yl 328 2-pyridylmethyl 329 3-pyridylmethyl 330 4-pyridylmethyl 331 4-chloropyridin-2-ylmethyl 332 5-chloropyridin-2-ylmethyl 333 6-chloropyridin-2-ylmethyl 334 5-chloropyridin-3-ylmethyl 335 6-chloropyridin-3-ylmethyl 336 2-chloropyridin-4-ylmethyl 337 2-pyrimidinylmethyl 338 4-chloropyrimidin-2-ylmethyl 339 5-chloropyrimidin-2-ylmethyl 340 2-chloropyrimidin-4-ylmethyl 341 6-chloropyrimidin-4-ylmethyl 342 2-chloropyrimidin-5-ylmethyl 343 4-pyridazinylmethyl 344 2-pyrazinylmethyl 345 5-chloropyrazin-2-ylmethyl 346 6-chloropyrazin-2-ylmethyl 347 3-pyridazinylmethyl 348 6-chloropyridazin-3-ylmethyl 349 1,3,5-triazinylmethyl 350 2-furylmethyl 351 3-furylmethyl 352 4-bromofur-2-ylmethyl 353 5-chlorofur-2-ylmethyl 354 2-thienylmethyl 355 3-thienylmethyl 356 5-methylthien-3-ylmethyl 357 5-chlorothien-2-ylmethyl 358 2-chlorothien-4-ylmethyl 359 2-pyrrolylmethyl 360 3-pyrrolylmethyl 361 2-oxazolylmethyl 362 4-methyloxazol-2-ylmethyl 363 5-methyloxazol-2-ylmethyl 364 4-chlorooxazol-2-ylmethyl 365 5-chlorooxazol-2-ylmethyl 366 4-oxazolylmethyl 367 2-methyloxazol-4-ylmethyl 368 5-methyloxazol-4-ylmethyl 369 2-chlorooxazol-4-ylmethyl 370 5-chlorooxazol-4-ylmethyl 371 5-oxazolylmethyl 372 2-methyloxazol-5-ylmethyl 373 4-methyloxazol-5-ylmethyl 374 2-chlorooxazol-5-ylmethyl 375 4-chlorooxazol-5-ylmethyl 376 2-thiazolylmethyl 377 4-methylthiazol-2-ylmethyl 378 5-methylthiazol-2-ylmethyl 379 4-chlorothiazol-2-ylmethyl 380 5-chlorothiazol-2-ylmethyl 381 4-thiazolylmethyl 382 2-methylthiazol-4-ylmethyl 383 5-methylthiazol-4-ylmethyl 384 2-chlorothiazol-4-ylmethyl 385 5-chlorothiazol-4-ylmethyl 386 5-thiazolylmethyl 387 2-methylthiazol-5-ylmethyl 388 4-methylthiazol-5-ylmethyl 389 2-chlorothiazol-5-ylmethyl 390 4-chlorothiazol-5-ylmethyl 391 3-isoxazolylmethyl 392 4-methylisoxazol-3-ylmethyl 393 5-methylisoxazol-3-ylmethyl 394 4-chloroisoxazol-3-ylmethyl 395 5-chloroisoxazol-3-ylmethyl 396 4-isoxazolylmethyl 397 3-methylisoxazol-4-ylmethyl 398 5-methylisoxazol-4-ylmethyl 399 3-chloroisoxazol-4-ylmethyl 400 5-chloroisoxazol-4-ylmethyl 401 5-isoxazolylmethyl 402 3-methylisoxazol-5-ylmethyl 403 4-methylisoxazol-5-ylmethyl 404 3-chloroisoxazol-5-ylmethyl 405 4-chloroisoxazol-5-ylmethyl 406 3-isothiazolylmethyl 407 4-methylisothiazol-3-ylmethyl 408 5-methylisothiazol-3-ylmethyl 409 4-chloroisothiazol-3-ylmethyl 410 5-chloroisothiazol-3-ylmethyl 411 4-isothiazolylmethyl 412 3-methylisothiazol-4-ylmethyl 413 5-methylisothiazol-4-ylmethyl 414 3-chloroisothiazol-4-ylmethyl 415 5-chloroisothiazol-4-ylmethyl 416 5-isothiazolylmethyl 417 3-methylisothiazol-5-ylmethyl 418 4-methylisothiazol-5-ylmethyl 419 3-chloroisothiazol-5-ylmethyl 420 4-chloroisothiazol-5-ylmethyl 421 4-imidazolylmethyl 422 1-phenylpyrazol-3-ylmethyl 423 1-methylimidazol-4-ylmethyl 424 1-phenyl-1,2,4-triazol-3-ylmethyl 425 1,2,4-oxadiazol-3-ylmethyl 426 5-chloro-1,2,4-oxadiazol-3-ylmethyl 427 5-methyl-1,2,4-oxadiazol-3-ylmethyl 428 5-trifluoromethyl-1,2,4-oxadiazol-3-ylmethyl 429 1,3,4-oxadiazol-2-ylmethyl 430 5-chloro-1,3,4-oxadiazol-2-ylmethyl 431 5-methyl-1,3,4-oxadiazol-2-ylmethyl 432 5-methoxy-1,3,4-oxadiazol-2-ylmethyl 433 1,2,4-thiadiazol-3-ylmethyl 434 5-chloro-1,2,4-thiadiazol-3-ylmethyl 435 5-methyl-1,2,4-thiadiazol-3-ylmethyl 436 1,3,4-thiadiazol-2-ylmethyl 437 5-chloro-1,3,4-thiadiazol-2-ylmethyl 438 5-methyl-1,3,4-thiadiazol-2-ylmethyl 439 5-cyano-1,3,4-thiadiazol-2-ylmethyl 440 2-(2'-pyridinyloxy)eth-1-yl 441 2-(3'-pyridinyloxy)eth-1-yl 442 2-(4'-pyridinyloxy)eth-1-yl 443 2-(2'-pyrimidinyloxy)eth-1-yl 444 2-(4'-pyrimidinyloxy)eth-1-yl 445 2-(5'-pyrimidinyloxy)eth-1-yl 446 2-(2'-pyrazinyloxy)eth-1-yl 447 2-(2'-pyridazinyloxy)eth-1-yl 448 2-(3'-pyridazinyloxy)eth-1-yl 449 2-(1',3',5'-triazinyloxy)eth-1-yl 450 2-(5'-methylisoxazol-3'-yloxy)eth-1-yl 451 2-(5'-chloroisoxazol-3'-yloxy)eth-1-yl 452 2-(2'-methoxythiazol-4'-yloxy)eth-1-yl 453 2-(4'-chlorooxazol-2'-yloxy)eth-1-yl 454 2-(1'-phenyl-1'H-1',2',4'-triazol-3'-yloxy)eth-1-yl 455 2-(1'-phenylpyrazol-3'-yloxy)eth-1-yl 456 C.sub.6 H.sub.5 457 2-F--C.sub.6 H.sub.4 458 3-F--C.sub.6 H.sub.4 459 4-F--C.sub.6 H.sub.4 460 2,3-F.sub.2 --C.sub.6 H.sub.3 461 2,4-F.sub.2 --C.sub.6 H.sub.3 462 2,5-F.sub.2 --C.sub.6 H.sub.3 463 2,6-F.sub.2 --C.sub.6 H.sub.3 464 3,4-F.sub.2 --C.sub.6 H.sub.3 465 3,5-F.sub.2 --C.sub.6 H.sub.3 466 2-Cl--C.sub.6 H.sub.4 467 3-Cl--C.sub.6 H.sub.4 468 4-Cl--C.sub.6 H.sub.4 469 2,3-Cl.sub.2 --C.sub.6 H.sub.3 470 2,4-Cl.sub.2 --C.sub.6 H.sub.3 471 2,5-Cl.sub.2 --C.sub.6 H.sub.3 472 2,6-Cl.sub.2 --C.sub.6 H.sub.3 473 3,4-Cl.sub.2 --C.sub.6 H.sub.3 474 3,5-Cl.sub.2 --C.sub.6 H.sub.3 475 2,3,4-Cl.sub.3 --C.sub.6 H.sub.2 476 2,3,5-Cl.sub.3 --C.sub.6 H.sub.2 477 2,3,6-Cl.sub.3 --C.sub.6 H.sub.2 478 2,4,5-Cl.sub.3 --C.sub.6 H.sub.2 479 2,4,6-Cl.sub.3 --C.sub.6 H.sub.2 480 3,4,5-Cl.sub.3 --C.sub.6 H.sub.2 481 2-Br--C.sub.6 H.sub.4 482 3-Br--C.sub.6 H.sub.4 483 4-Br--C.sub.6 H.sub.4 484 2,3-Br.sub.2 --C.sub.6 H.sub.3 485 2,4-Br.sub.2 --C.sub.6 H.sub.3 486 2,5-Br.sub.2 --C.sub.6 H.sub.3 487 2,6-Br.sub.2 --C.sub.6 H.sub.3 488 3,4-Br.sub.2 --C.sub.6 H.sub.3 489 3,5-Br.sub.2 --C.sub.6 H.sub.3 490 2-F, 3-Cl--C.sub.6 H.sub.3 491 2-F, 4-Cl--C.sub.6 H.sub.3 492 2-F, 5-Cl--C.sub.6 H.sub.3 493 2-F, 3-Br--C.sub.6 H.sub.3 494 2-F, 4-Br--C.sub.6 H.sub.3 495 2-F, 5-Br--C.sub.6 H.sub.3 496 2-Cl, 3-Br--C.sub.6 H.sub.3 497 2-Cl, 4-Br--C.sub.6 H.sub.3 498 2-Cl, 5-Br--C.sub.6 H.sub.3 499 3-F, 4-Cl--C.sub.6 H.sub.3 500 3-F, 5-Cl--C.sub.6 H.sub.3 501 3-F, 6-Cl--C.sub.6 H.sub.3 502 3-F, 4-Br--C.sub.6 H.sub.3 503 3-F, 5-Br--C.sub.6 H.sub.3 504 3-F, 6-Br--C.sub.6 H.sub.3 505 3-Cl, 4-Br--C.sub.6 H.sub.3 506 3-Cl, 5-Br--C.sub.6 H.sub.3 507 3-Cl, 6-Br--C.sub.6 H.sub.3 508 4-F, 5-Cl--C.sub.6 H.sub.3 509 4-F, 6-Cl--C.sub.6 H.sub.3 510 4-F, 5-Br--C.sub.6 H.sub.3 511 4-F, 6-Br--C.sub.6 H.sub.3 512 4-Cl, 5-Br--C.sub.6 H.sub.3 513 5-F, 6-Cl--C.sub.6 H.sub.3 514 5-F, 6-Br--C.sub.6 H.sub.3 515 5-Cl, 6-Br--C.sub.6 H.sub.3 516 3-Br, 4-Cl, 5-Br--C.sub.6 H.sub.2 517 2-CN--C.sub.6 H.sub.4 518 3-CN--C.sub.6 H.sub.4 519 4-CN--C.sub.6 H.sub.4 520 2-NO.sub.2 --C.sub.6 H.sub.4 521 3-NO.sub.2 --C.sub.6 H.sub.4 522 4-NO.sub.2 --C.sub.6 H.sub.4 523 2-CH.sub.3 --C.sub.6 H.sub.4 524 3-CH.sub.3 --C.sub.6 H.sub.4 525 4-CH.sub.3 --C.sub.6 H.sub.4 526 2,3-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 527 2,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 528 2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 529 2,6-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 530 3,4-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 531 3,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 532 2-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 533 3-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 534 4-C.sub.2 H.sub.5 --C.sub.6 H.sub.4 535 2-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 536 3-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 537 4-i-C.sub.3 H.sub.7 --C.sub.6 H.sub.4 538 3-tert-C.sub.4 H.sub.9 --C.sub.6 H.sub.4 539 4-tert-C.sub.4 H.sub.9 --C.sub.6 H.sub.4 540 2-vinyl-C.sub.6 H.sub.4 541 3-vinyl-C.sub.6 H.sub.4 542 4-vinyl-C.sub.6 H.sub.4 543 2-allyl-C.sub.6 H.sub.4 544 3-allyl-C.sub.6 H.sub.4 545 4-allyl-C.sub.6 H.sub.4 546 2-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 547 3-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 548 4-C.sub.6 H.sub.5 --C.sub.6 H.sub.4 549 3-CH.sub.3, 5-tert-C.sub.4 H.sub.9 --C.sub.6 H.sub.3 550 2-OH--C.sub.6 H.sub.4 551 3-OH--C.sub.6 H.sub.4 552 4-OH--C.sub.6 H.sub.4 553 2-OCH.sub.3 --C.sub.6 H.sub.4 554 3-OCH.sub.3 --C.sub.6 H.sub.4 555 4-OCH.sub.3 --C.sub.6 H.sub.4 556 2,3-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 557 2,4-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 558 2,5-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 559 3,4-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 560 3,5-(OCH.sub.3).sub.2 --C.sub.6 H.sub.3 561 3,4,5-(OCH.sub.3)3-C.sub.6 H.sub.2 562 2-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 563 3-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 564 4-OC.sub.2 H.sub.5 --C.sub.6 H.sub.4 565 2-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 566 3-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 567 4-O-(n-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 568 2-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 569 3-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 570 4-O-(i-C.sub.3 H.sub.7)--C.sub.6 H.sub.4 571 4-O-(n-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 572 3-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 573 4-O-(t-C.sub.4 H.sub.9)--C.sub.6 H.sub.4 574 2-O-allyl-C.sub.6 H.sub.4 575 3-O-allyl-C.sub.6 H.sub.4 576 4-O-allyl-C.sub.6 H.sub.4 577 2-CF.sub.3 --C.sub.6 H.sub.4 578 3-CF.sub.3 --C.sub.6 H.sub.4 579 4-CF.sub.3 --C.sub.6 H.sub.4 580 2-acetyl-C.sub.6 H.sub.4 581 3-acetyl-C.sub.6 H.sub.4 582 4-acetyl-C.sub.6 H.sub.4 583 2-methoxycarbonyl-C.sub.6 H.sub.4 584 3-methoxycarbonyl-C.sub.6 H.sub.4 585 4-methoxycarbonyl-C.sub.6 H.sub.4 586 2-aminocarbonyl-C.sub.6 H.sub.4 587 3-aminocarbonyl-C.sub.6 H.sub.4 588 4-aminocarbonyl-C.sub.6 H.sub.4 589 2-dimethylaminocarbonyl-C.sub.6 H.sub.4 590 3-dimethylaminocarbonyl-C.sub.6 H.sub.4 591 4-dimethylaminocarbonyl-C.sub.6 H.sub.4 592 2-(N-methylaminocarbonyl)-C.sub.6 H.sub.4 593 3-(N-methylaminocarbonyl)-C.sub.6 H.sub.4 594 4-(N-methylaminocarbonyl)-C.sub.6 H.sub.4 595 2-H.sub.2 N--C.sub.6 H.sub.4 596 3-H.sub.2 N--C.sub.6 H.sub.4 597 4-H.sub.2 N--C.sub.6 H.sub.4 598 2-aminothiocarbonyl-C.sub.6 H.sub.4 599 3-aminothiocarbonyl-C.sub.6 H.sub.4 600 4-aminothiocarbonyl-C.sub.6 H.sub.4 601 2-methoxyiminomethyl-C.sub.6 H.sub.4 602 3-methoxyiminomethyl-C.sub.6 H.sub.4 603 4-methoxyiminomethyl-C.sub.6 H.sub.4 604 3,4-methylenedioxy-C.sub.6 H.sub.3 605 3,4-difluoromethylenedioxy-C.sub.6 H.sub.3 606 2,3-methylenedioxy-C.sub.6 H.sub.3 607 2-(1'-methoxyiminoeth-1'-yl)-C.sub.6 H.sub.4 608 3-(1'-methoxyiminoeth-1'-yl)-C.sub.6 H.sub.4 609 4-(1'-methoxyiminoeth-1'-yl)-C.sub.6 H.sub.4 610 2-SCH.sub.3 --C.sub.6 H.sub.4 611 3-SCH.sub.3 --C.sub.6 H.sub.4 612 4-SCH.sub.3 --C.sub.6 H.sub.4 613 2-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 614 3-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 615 4-SO.sub.2 CH.sub.3 --C.sub.6 H.sub.4 616 2-OCF.sub.3 --C.sub.6 H.sub.4 617 3-OCF.sub.3 --C.sub.6 H.sub.4 618 4-OCF.sub.3 --C.sub.6 H.sub.4 619 2-OCHF.sub.2 --C.sub.6 H.sub.4 620 3-OCHF.sub.2 --C.sub.6 H.sub.4 621 4-OCHF.sub.2 --C.sub.6 H.sub.4 622 3-CF.sub.3, 4-OCF.sub.3 --C.sub.6 H.sub.3 623 2-NHCH.sub.3 --C.sub.6 H.sub.4 624 3-NHCH.sub.3 --C.sub.6 H.sub.4 625 4-NHCH.sub.3 --C.sub.6 H.sub.4 626 2-N(CH.sub.3 ).sub.2 --C.sub.6 H.sub.4 627 3-N(CH.sub.3 ).sub.2 --C.sub.6 H.sub.4 628 4-N(CH.sub.3 ).sub.2 --C.sub.6 H.sub.4 629 2-ethoxycarbonyl-C.sub.6 H.sub.4 630 3-ethoxycarbonyl-C.sub.6 H.sub.4 631 4-ethoxycarbonyl-C.sub.6 H.sub.4 632 2-CH.sub.2 CH.sub.2 F--C.sub.6 H.sub.4 633 3-CH.sub.2 CH.sub.2 F--C.sub.6 H.sub.4 634 4-CH.sub.2 CH.sub.2 F--C.sub.6 H.sub.4 635 2-CH.sub.2 CF.sub.3 --C.sub.6 H.sub.4 636 3-CH.sub.2 CF.sub.3 --C.sub.6 H.sub.4 637 4-CH.sub.2 CF.sub.3 --C.sub.6 H.sub.4 638 2-CF.sub.2 CHF.sub.2 --C.sub.6 H.sub.4 639 3-CF.sub.2 CHF.sub.2 --C.sub.6 H.sub.4 640 4-CF.sub.2 CHF.sub.2 --C.sub.6 H.sub.4 641 2-CHF.sub.2 --C.sub.6 H.sub.4 642 3-CHF.sub.2 --C.sub.6 H.sub.4 643 4-CHF.sub.2 --C.sub.6 H.sub.4 644 2-(1'-oxo-n-prop-1-yl)-C.sub.6 H.sub.4 645 3-(1'-oxo-n-prop-1-yl)-C.sub.6 H.sub.4 646 4-(1'-oxo-n-prop-1-yl)-C.sub.6 H.sub.4 647 2-(1'-oxoisoprop-1-yl)-C.sub.6 H.sub.4 648 3-(1'-oxoisoprop-1-yl)-C.sub.6 H.sub.4 649 4-(1'-oxoisoprop-1-yl)-C.sub.6 H.sub.4 650 3-cyclopropyl-C.sub.6 H.sub.4 651 4-cyclopropyl-C.sub.6 H.sub.4 652 4-cyclohexyl-C.sub.6 H.sub.4 653 1-naphthyl 654 2-naphthyl 655 2-pyridyl 656 3-pyridyl 657 4-pyridyl 658 5-CH.sub.3 -pyridin-2-yl 659 5-Cl-pyridin-2-yl 660 6-Cl-pyridin-2-yl 661 3,5-Cl.sub.2 -pyridin-2-yl 662 6-OCH.sub.3 -pyridin-2-yl 663 6-CH.sub.3 -pyridin-2-yl 664 6-Cl-pyridin-3-yl 665 6-CH.sub.3 -pyridin-3-yl 666 6-OCH.sub.3 -pyridin-3-yl 667 2-pyrimidinyl 668 4-OCH.sub.3 -pyrimidin-2-yl 669 4-OC.sub.2 H.sub.5 -pyrimidin-2-yl 670 4-Cl-pyrimidin-2-yl 671 4-CH.sub.3 -pyrimidin-2-yl 672 5-CH.sub.3 -pyrimidin-2-yl 673 5-Cl-pyrimidin-2-yl 674 5-OCH.sub.3 -pyrimidin-2-yl 675 5-OC.sub.2 H.sub.5 -pyrimidin-2-yl 676 4-pyrimidinyl 677 2-Cl-pyrimidin-4-yl 678 2-OCH.sub.3 -pyrimidin-4-yl 679 2-CH.sub.3 -pyrimidin-4-yl 680 6-Cl-pyrimidin-4-yl 681 6-CH.sub.3 -pyrimidin-4-yl 682 6-OCH.sub.3 -pyrimidin-4-yl 683 5-pyrimidinyl 684 2-CH.sub.3 -pyrimidin-5-yl 685 2-Cl-pyrimidin-5-yl 686 2-OCH.sub.3 -pyrimidin-5-yl 687 2-OC.sub.2 H.sub.5 -pyrimidin-5-yl 688 2-furyl 689 4-C.sub.2 H.sub.5 -fur-2-yl 690 4-CH.sub.3 -fur-2-yl 691 4-Cl-fur-2-yl 692 4-CN-fur-2-yl 693 5-CH.sub.3 -fur-2-yl 694 5-Cl-fur-2-yl 695 5-CN-fur-2-yl 696 3-furyl 697 5-CH.sub.3 -fur-3-yl 698 5-Cl-fur-3-yl 699 5-CN-fur-3-yl 700 2-thienyl 701 4-CH.sub.3 -thien-2-yl 702 4-Cl-thien-2-yl 703 4-CN-thien-2-yl 704 5-CH.sub.3 -thien-2-yl 705 5-Cl-thien-2-yl 706 5-CN-thien-2-yl 707 3-thienyl 708 5-CH.sub.3 -thien-3-yl 709 5-Cl-thien-3-yl 710 5-CN-thien-3-yl 711 4-CH.sub.3 -thien-3-yl 712 5-F-thien-3-yl 713 2-oxazolyl 714 4-CH.sub.3 -oxazol-2-yl 715 4-Cl-oxazol-2-yl 716 4-CN-oxazol-2-yl 717 5-CH.sub.3 -oxazol-2-yl 718 5-Cl-oxazol-2-yl 719 5-CN-oxazol-2-yl 720 4-oxazolyl 721 2-CH.sub.3 -oxazol-4-yl 722 2-Cl-oxazol-4-yl 723 2-CN-oxazol-4-yl 724 5-oxazolyl 725 2-CH.sub.3 -oxazol-5-yl 726 2-Cl-oxazol-5-yl 727 2-CN-oxazol-5-yl 728 3-isoxazolyl 729 5-CH.sub.3 -isoxazol-3-yl 730 5-Cl-isoxazol-3-yl 731 5-CN-isoxazol-3-yl 732 5-isoxazolyl 733 3-CH.sub.3 -isoxazol-5-yl 734 3-Cl-isoxazol-5-yl 735 3-CN-isoxazol-5-yl 736 2-thiazolyl 737 4-CH.sub.3 -thiazol-2-yl 738 4-Cl-thiazol-2-yl 739 4-CN-thiazol-2-yl 740 5-CH.sub.3 -thiazol-2-yl 741 5-Cl-thiazol-2-yl 742 5-CN-thiazol-2-yl 743 4-thiazolyl 744 2-CH.sub.3 -thiazol-4-yl 745 2-Cl-thiazol-4-yl 746 2-CN-thiazol-4-yl 747 2-SCH.sub.3 -thiazol-4-yl 748 5-thiazolyl 749 2-CH.sub.3 -thiazol-5-yl 750 2-Cl-thiazol-5-yl 751 2-CN-thiazol-5-yl 752 3-isothiazolyl 753 5-CH.sub.3 -isothiazol-3-yl 754 5-Cl-isothiazol-3-yl 755 5-CN-isothiazol-3-yl 756 5-isothiazolyl 757 3-CH.sub.3 -isothiazol-5-yl 758 3-Cl-isothiazol-5-yl 759 3-CN-isothiazol-5-yl 760 2-imidazolyl 761 4-CH.sub.3 -imidazol-2-yl 762 4-Cl-imidazol-2-yl 763 4-CN-imidazol-2-yl 764 1-CH.sub.3 -imidazol-2-yl 765 1-CH.sub.3, 4-Cl-imidazol-2-yl 766 1,4-(CH.sub.3 ).sub.2 -imidazol-2-yl 767 1-CH.sub.3, 5-Cl-imidazol-2-yl 768 1,5-(CH.sub.3 ).sub.2 -imidazol-2-yl 769 4-imidazolyl 770 2-CH.sub.3 -imidazol-4-yl 771 2-Cl-imidazol-4-yl 772 1-CH.sub.3 -imidazol-4-yl 773 1,2-(CH.sub.3 ).sub.2 -imidazol-4-yl 774 1-CH.sub.3 1 2-Cl-imidazol-4-yl 775 1-CH.sub.3 -imidazol-5-yl 776 1-CH.sub.3 1 3-Cl-imidazol-5-yl 777 1,2-(CH.sub.3 ).sub.2 -imidazol-5-yl 778 3-pyrazolyl 779 5-CH.sub.3 -pyrazol-3-yl 780 5-Cl-pyrazol-3-yl 781 5-CN-pyrazol-3-yl 782 1-CH.sub.3 -pyrazol-3-yl 783 1-CH.sub.3 1 4-Cl-pyrazol-3-yl 784 1-CH.sub.3 1 5-Cl-pyrazol-3-yl 785 1,5-(CH.sub.3 ).sub.2 -pyrazol-3-yl 786 1-CH.sub.3 -pyrazol-5-yl 787 1-CH.sub.3 1 3-Cl-pyrazol-5-yl 788 1,3-(CH.sub.3 ).sub.2 -pyrazol-5-yl 789 4-pyrazolyl 790 3-Cl-pyrazol-4-yl 791 3-CH.sub.3 -pyrazol-4-yl 792 1-CH.sub.3 -pyrazol-4-yl 793 1-CH.sub.3, 3-Cl-pyrazol-4-yl 794 1,3-(CH.sub.3 ).sub.2 -pyrazol-4-yl 795 1,3,4-oxadiazol-5-yl 796 2-CH.sub.3 -1,3,4-oxadiazol-5-yl 797 2-Cl-1,3,4-oxadiazol-5-yl 798 2-CF.sub.3 -1,3,4-oxadiazol-5-yl 799 2-i-C.sub.3 H.sub.7 -1,3,4-oxadiazol-5-yl 800 2-OCH.sub.3 -1,3,4-oxadiazol-5-yl 801 1,2,4-oxadiazol-3-yl 802 5-CH.sub.3 -1,2,4-oxadiazol-3-yl 803 5-i-C.sub.3 H.sub.7 -1,2,4-oxadiazol-3-yl 804 5-Cl-1,2,4-oxadiazol-3-yl 805 5-CF.sub.3 -1,2,4-oxadiazol-3-yl 806 1,2,4-triazol-3-yl 807 1-CH.sub.3 -1,2,4-triazol-3-yl 808 3-fluoropyridin-2-yl 809 3-chloropyridin-2-yl 810 3-bromopyridin-2-yl 811 3-methylpyridin-2-yl 812 3-trifluoromethylpyridin-2-yl 813 3-methoxypyridin-2-yl 814 4-fluoropyridin-2-yl 815 4-chloropyridin-2-yl 816 4-bromopyridin-2-yl 817 4-methylpyridin-2-yl 818 4-trifluoromethylpyridin-2-yl 819 4-methoxypyridin-2-yl 820 5-fluoropyridin-2-yl 821 5-bromopyridin-2-yl 822 6-trifluoromethylpyridin-2-yl 823 2-fluoropyridin-3-yl 824 2-chloropyridin-3-yl 825 2-bromopyridin-3-yl 826 2-methylpyridin-3-yl 827 2-trifluoromethylpyridin-3-yl 828 3-methoxypyridin-3-yl 829 4-fluoropyridin-3-yl 830 4-chloropyridin-3-yl 831 4-bromopyridin-3-yl 832 4-methylpyridin-3-yl 833 4-trifluoromethylpyridin-3-yl 834 4-methoxypyridin-3-yl 835 5-fluoropyridin-3-yl 836 5-chloropyridin-3-yl 837 5-bromopyridin-3-yl 838 5-methylpyridin-3-yl 839 5-trifluoromethylpyridin-3-yl 840 5-methoxypyridin-3-yl 841 6-fluoropyridin-3-yl 842 6-bromopyridin-3-yl 843 6-trifluoromethylpyridin-3-yl 844 2-fluoropyridin-4-yl 845 2-chloropyridin-4-yl 846 2-bromopyridin-4-yl 847 2-methylpyridin-4-yl 848 2-trifluoromethylpyridin-4-yl 849 2-methoxypyridin-4-yl 850 3-fluoropyridin-4-yl 851 3-chloropyridin-4-yl 852 3-bromopyridin-4-yl 853 3-methylpyridin-4-yl 854 3-trifluoromethylpyridin-4-yl 855 3-methoxypyridin-4-yl 856 4-fluoropyrimidin-2-yl 857 4-bromopyrimidin-2-yl 858 4-trifluoromethylpyrimidin-2-yl 859 5-fluoropyrimidin-2-yl 860 5-bromopyrimidin-2-yl 861 5-trifluoromethylpyrimidin-2-yl 862 2-fluoropyrimidin-4-yl 863 2-bromopyrimidin-4-yl 864 2-trifluoromethylpyrimidin-4-yl 865 2-trifluoromethoxypyrimidin-4-yl 866 5-fluoropyrimidin-4-yl 867 5-chloropyrimidin-4-yl 868 5-bromopyrimidin-4-yl 869 5-methoxypyrimidin-4-yl 870 5-trifluoromethylpyrimidin-4-yl 871 5-methoxypyrimidin-4-yl 872 6-fluoropyrimidin-4-yl 873 6-bromopyrimidin-4-yl 874 6-trifluoromethylpyrimidin-4-yl 875 2-fluoropyrimidin-5-yl 876 2-bromopyrimidin-5-yl 877 2-trifluoromethylpyrimidin-5-yl 878 4-fluoropyrimidin-5-yl 879 4-chloropyrimidin-5-yl 880 4-bromopyrimidin-5-yl 881 4-methylpyrimidin-5-yl 882 4-trifluoromethylpyrimidin-5-yl 883 3-fluoro-5-trifluoromethylpyridin-2-yl 884 3,6-dichloro-5-trifluoromethylpyridin-2-yl 885 5,6-dichloro-3-trifluoromethylpyridin-2-yl 886 5-chloro-3-trifluoromethylpyridin-2-yl 887 3-chloro-5-trifluoromethylpyridin-2-yl 888 6-chloro-4-cyanopyridin-2-yl 889 3-cyano-5-nitropyridin-2-yl 890 2-chloro-6-fluoropyridin-4-yl 891 6-chloro-4-fluoropyridin-2-yl 892 4,6-difluoropyridin-2-yl 893 3,5-dichloro-6-fluoropyridin-2-yl 894 6-methoxy-3-nitropyridin-2-yl 895 4-cyano-6-fluoropyridin-2-yl 896 6-chloro-5-cyanopyridin-2-yl 897 6-chloro-3-cyanopyridin-2-yl 898 4-cyano-3,5,6-trifluoropyridin-2-yl 899 6-chloro-5-nitropyridin-2-yl 900 6-chloro-3-nitropyridin-2-yl 901 5-cyano-6-fluoropyridin-2-yl 902 3-cyano-6-fluoropyridin-2-yl 903 4,6-dicyanopyridin-2-yl 904 5-trichloromethylpyridin-2-yl 905 5-cyanopyridin-2-yl 906 5-bromo-4-trifluoromethylpyridin-2-yl 907 3-nitro-5-trifluoromethylpyridin-2-yl 908 5-aminopyridin-2-yl 909 2,3,5,6-tetrafluoropyridin-4-yl 910 5-nitropyridin-2-yl 911 4-methyl-5-nitroypridin-2-yl 912 5-difluoromethylpyridin-2-yl 913 5-fluoromethylpyridin-2-yl 914 4,6-difluoropyrimidin-2-yl 915 2,6-difluoropyrimidin-4-yl 916 2-chloro-6-trichloromethylpyrimidin-4-yl 917 2,6-dichloropyrimidin-4-yl 918 5-methoxycarbonylpyridin-2-yl 919 5-chloro-6-fluoropyridin-2-yl 920 5-chloro-6-hydroxypyridin-2-yl 921 5-chloro-6-methoxypyridin-2-yl 922 5-chloro-cyanopyridin-2-yl 923 5,6-dichloropyridin-2-yl 924 6-bromo-5-chloropyridin-2-yl 925 5-bromo-6-fluoropyridin-2-yl 926 5-bromo-6-chloropyridin-2-yl 927 5-bromo-6-cyanopyridin-2-yl 928 5-bromo-6-hydroxypyridin-2-yl 929 5-bromo-6-methoxypyridin-2-yl 930 5,6-dibromopyridin-2-yl 931 4-cyanopyridin-2-yl 932 6-cyanopyridin-2-yl 933 4-chloro-6-methylpyrimidin-2-yl 934 2-chloro-fluoropyridin-4-yl 935 5-bromo-4-trifluoromethylpyridin-2-yl 936 4,5-dichloropyridin-2-yl 937 4,5-dibromopyridin-2-yl 938 5,6-dichloropyridin-2-yl 939 4,6-dichloropyridin-2-yl 940 4,6-dibromopyridin-2-yl 941 5,6-dibromopyridin-2-yl 942 4-bromo-5-chloropyridin-2-yl 943 6-bromo-5-chloropyridin-2-yl 944 5-bromo-4-chloropyridin-2-yl 945 5-bromo-4-chloropyridin-2-yl 946 6-bromo-4-chloropyridin-2-yl 947 4-bromo-6-chloropyridin-2-yl 948 6-chloro-4-methoxypyridin-2-yl 949 6-bromo-4-methoxypyridin-2-yl 950 6-chlorochinazolin-2-yl 951 quinazolin-2-yl 952 4-cyanopyridin-2-yl 953 6-cyanopyridin-2-yl 954 5-hydroxymethylpyridin-2-yl 955 6-chloro-4-trifluoromethylpyridin-2-yl 956 6-chloro-4-trifluoromethylpyridin-2-yl 957 6-chloro-4-methylpyridin-2-yl 958 2,5-dichloro-6-cyanopyridin-2-yl 959 2,5-dichloro-6-carboxypyridin-2-yl 960 2,5-dichloro-6-methoxycarbonyl-pyridin-2-yl 961 6-trifluoromethylpyridin-2-yl 962 6-methoxycarbonylpyridin-2-yl 963 6-carboxypyridin-2-yl 964 4-phenoxypyridin-2-yl 965 5-phenoxypyridin-2-yl 966 6-phenoxypyridin-2-yl 967 4-phenoxypyrimidin-4-yl 968 4-(4-methylphenoxy)pyrimidin-4-yl 969 4-phenoxypyrimidin-2-yl 970 4-(2-fluorophenoxy)pyrimidin-2-yl 971 4-phenoxypyrimidin-6-yl 972 4-(4-chlorophenoxy)pyrimidin-6-yl 973 4-(2-pyridyloxy)pyrimidin-6-yl 974 4-(6-chloro-2-pyridyloxy)pyrimidin-6-yl 975 4-(3-pyridyloxy)pyrimidin-6-yl 976 4-(2-methyl-3-pyridyloxy)pyrimidin-6-yl 977 4-(4-pyridyloxy)pyrimidin-6-yl 978 5-bromo-2-thienyl 979 5-nitro-2-thienyl 980 2-chloro-3-thienyl 981 2-bromo-3-thienyl 982 1-methyl-3-pyrrolyl 983 1-methyl-2-pyrrolyl 984 1-benzofuran-2-yl 985 1-benzofuran-3-yl 986 1-benzothiophen-2-yl 987 1-benzothiophen-3-yl 988 3-pyrrolyl 989 2-pyrrolyl 990 3-indolyl 991 2-indolyl 992 1-methyl-3-indolyl 993 1-methyl-2-indolyl 994 isoxazol-4-yl 995 isothiazol-4-yl 996 1,2-benzisoxazol-3-yl 997 1,2-benzisothiazol-3-yl 998 1-methylindazol-3-yl 999 benzoxazol-2-yl 1000 5-chlorobenzoxazol-2-yl 1001 6-fluorobenzoxazol-2-yl 1002 benzthiazol-2-yl 1003 5-fluorobenzthiazol-2-yl 1004 6-fluorobenzthiazol-2-yl 1005 pyrido[3,2-d]thiazol-2-yl 1006 (6-chloropyrido) [3, 2-d]thiazol-2-yl 1007 1-methyl-1,2,3-triazol-5-yl 1008 1-methyl-1,2,3-triazol-4-yl 1009 1-methyl-1,2,4-triazol-5-yl 1010 1-methyl-1,2,3,4-tetrazol-5-yl 1011 2-methyl-1,2,3,4-tetrazol-5-yl 1012 5-trifluoromethyl-1,3,4-thiadiazol-2-yl 1013 6-chlorobenzoxazol-2-yl 1014 5-fluorobenzoxazol-2-yl 1015 5-nitrothiazol-2-yl 1016 1-CH(CH.sub.3).sub.2 -pyrrol-3-yl 1017 1-C(CH.sub.3).sub.3 -pyrrol-3-yl 1018 1-cyclopropylpyrrol-3-yl 1019 1-C.sub.6 H.sub.5 -pyrrol-3-yl 1020 1-(2-CH.sub.3 --C.sub.6 H.sub.4)pyrrol-3-yl 1021 1-(3-CH.sub.3 --C.sub.6 H.sub.4)pyrrol-3-yl 1022 1-(4-CH.sub.3 --C.sub.6 H.sub.4)pyrrol-3-yl 1023 1-(3-OCH.sub.3 --C.sub.6 H.sub.4)pyrrol-3-yl 1024 1-(4-OCH.sub.3 --C.sub.6 H.sub.4)pyrrol-3-yl 1025 1-(4-NO.sub.2 --C.sub.6 H.sub.4)pyrrol-3-yl 1026 1-(3-NO.sub.2 --C.sub.6 H.sub.4)pyrrol-3-yl 1027 1-(4-CN--C.sub.6 H.sub.4)pyrrol-3-yl 1028 1-(3-CN--C.sub.6 H.sub.4)pyrrol-3-yl 1029 1-(3-CF.sub.3 --C.sub.6 H.sub.4)pyrrol-3-yl 1030 1-(4-CF.sub.3 --C.sub.6 H.sub.4)pyrrol-3-yl 1031 1-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)pyrrol-3-yl 1032 1-(2-Cl--C.sub.6 H.sub.4)pyrrol-3-yl 1033 1-(3-Cl--C.sub.6 H.sub.4)pyrrol-3-yl 1034 1-(4-Cl--C.sub.6 H.sub.4)pyrrol-3-yl 1035 1-(2-Br--C.sub.6 H.sub.4)pyrrol-3-yl 1036 1-(3-Br--C.sub.6 H.sub.4)pyrrol-3-yl 1037 1-(4-Br--C.sub.6 H.sub.4)pyrrol-3-yl 1038 1-(2-F--C.sub.6 H.sub.4)pyrrol-3-yl 1039 1-(3-F--C.sub.6 H.sub.4)pyrrol-3-yl 1040 1-(4-F--C.sub.6 H.sub.4)pyrrol-3-yl 1041 1-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)pyrrol-3-yl 1042 1-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)pyrrol-3-yl 1043 1-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)pyrrol-3-yl 1044 1-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)pyrrol-3-yl 1045 1-(2,4-F.sub.2 --C.sub.6 H.sub.3)pyrrol-3-yl 1046 1-(2,5-F.sub.2 --C.sub.6 H.sub.3)pyrrol-3-yl 1047 1-(2,6-F.sub.2 --C.sub.6 H.sub.3)pyrrol-3-yl 1048 1-(3,4-F.sub.2 --C.sub.6 H.sub.3)pyrrol-3-yl 1049 1-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)pyrrol-3-yl 1050 1-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)pyrrol-3-yl 1051 1-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)pyrrol-3-yl 1052 1-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)pyrrol-3-yl 1053 1-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]pyrrol-3-yl 1054 1-CH(CH.sub.3).sub.2 -pyrrol-2-yl 1055 1-C(CH.sub.3)3-pyrrol-2-yl 1056 1-cyclopropylpyrrol-2-yl 1057 1-C.sub.6 H.sub.5 -pyrrol-2-yl 1058 1-(2-CH.sub.3 --C.sub.6 H.sub.4)pyrrol-2-yl 1059 1-(3-CH.sub.3 --C.sub.6 H.sub.4)pyrrol-2-yl 1060 1-(4-CH.sub.3 --C.sub.6 H.sub.4)pyrrol-2-yl 1061 1-(3-OCH.sub.3 --C.sub.6 H.sub.4)pyrrol-2-yl 1062 1-(4-OCH.sub.3 --C.sub.6 H.sub.4)pyrrol-2-yl 1063 1-(4-NO.sub.2 --C.sub.6 H.sub.4)pyrrol-2-yl 1064 1-(3-NO.sub.2 --C.sub.6 H.sub.4)pyrrol-2-yl 1065 1-(4-CN--C.sub.6 H.sub.4)pyrrol-2-yl 1066 1-(3-CN--C.sub.6 H.sub.4)pyrrol-2-yl 1067 1-(3-CF.sub.3 --C.sub.6 H.sub.4)pyrrol-2-yl 1068 1-(4-CF.sub.3 --C.sub.6 H.sub.4)pyrrol-2-yl 1069 1-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)pyrrol-2-yl 1070 1-(2-Cl--C.sub.6 H.sub.4)pyrrol-2-yl 1071 1-(3-Cl--C.sub.6 H.sub.4)pyrrol-2-yl 1072 1-(4-Cl--C.sub.6 H.sub.4)pyrrol-2-yl 1073 1-(2-Br--C.sub.6 H.sub.4)pyrrol-2-yl 1074 1-(3-Br--C.sub.6 H.sub.4)pyrrol-2-yl 1075 1-(4-Br--C.sub.6 H.sub.4)pyrrol-2-yl 1076 1-(2-F--C.sub.6 H.sub.4)pyrrol-2-yl 1077 1-(3-F--C.sub.6 H.sub.4)pyrrol-2-yl 1078 1-(4-F--C.sub.6 H.sub.4)pyrrol-2-yl 1079 1-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)pyrrol-2-yl 1080 1-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)pyrrol-2-yl 1081 1-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)pyrrol-2-yl 1082 1-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)pyrrol-2-yl 1083 1-(2,4-F.sub.2 --C.sub.6 H.sub.3)pyrrol-2-yl 1084 1-(2,5-F.sub.2 --C.sub.6 H.sub.3)pyrrol-2-yl 1085 1-(2,6-F.sub.2 --C.sub.6 H.sub.3)pyrrol-2-yl 1086 1-(3,4-F.sub.2 --C.sub.6 H.sub.3)pyrrol-2-yl 1087 1-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)pyrrol-2-yl 1088 1-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)pyrrol-2-yl 1089 1-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)pyrrol-2-yl 1090 1-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)pyrrol-2-yl 1091 1-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]pyrrol-2-yl 1092 5-CH(CH.sub.3).sub.2 -furan-2-yl 1093 5-C(CH.sub.3).sub.3 -furan-2-yl 1094 5-cyclopropylfuran-2-yl 1095 5-C.sub.6 H.sub.5 -furan-2-yl 1096 5-(2-CH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1097 5-(3-CH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1098 5-(4-CH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1099 5-(3-OCH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1100 5-(4-OCH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1101 5-(4-NO.sub.2 --C.sub.6 H.sub.4)furan-2-yl 1102 5-(3-NO.sub.2 --C.sub.6 H.sub.4)furan-2-yl 1103 5-(4-CN--C.sub.6 H.sub.4)furan-2-yl 1104 5-(3-CN--C.sub.6 H.sub.4)furan-2-yl 1105 5-(3-CF.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1106 5-(4-CF.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1107 5-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)furan-2-yl 1108 5-(4-C.sub.6 H.sub.5 --C.sub.6 H.sub.4)furan-2-yl 1109 5-(2-Cl--C.sub.6 H.sub.4)furan-2-yl 1110 5-(3-Cl--C.sub.6 H.sub.4)furan-2-yl 1111 5-(4-Cl--C.sub.6 H.sub.4)furan-2-yl 1112 5-(2-Br--C.sub.6 H.sub.4)furan-2-yl 1113 5-(3-Br--C.sub.6 H.sub.4)furan-2-yl 1114 5-(4-Br--C.sub.6 H.sub.4)furan-2-yl 1115 5-(2-F--C.sub.6 H.sub.4)furan-2-yl 1116 5-(3-F--C.sub.6 H.sub.4)furan-2-yl 1117 5-(4-F--C.sub.6 H.sub.4)furan-2-yl 1118 5-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1119 5-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1120 5-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1121 5-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1122 5-(2,4-F.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1123 5-(2,5-F.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1124 5-(2,6-F.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1125 5-(3,4-F.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1126 5-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)furan-2-yl 1127 5-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)furan-2-yl 1128 5-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)furan-2-yl 1129 5-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)furan-2-yl 1130 5-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]furan-2-yl 1131 4-CH(CH.sub.3).sub.2 -furan-2-yl 1132 4-C(CH.sub.3).sub.3 -furan-2-yl 1133 4-cyclopropylfuran-2-yl 1134 4-C.sub.6 H.sub.5 -furan-2-yl 1135 4-(2-CH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1136 4-(3-CH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1137 4-(4-CH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1138 4-(3-OCH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1139 4-(4-OCH.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1140 4-(4-NO.sub.2 --C.sub.6 H.sub.4)furan-2-yl 1141 4-(3-NO.sub.2 --C.sub.6 H.sub.4)furan-2-yl 1142 4-(4-CN--C.sub.6 H.sub.4)furan-2-yl 1143 4-(3-CN--C.sub.6 H.sub.4)furan-2-yl 1144 4-(3-CF.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1145 4-(4-CF.sub.3 --C.sub.6 H.sub.4)furan-2-yl 1146 4-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)furan-2-yl 1147 4-(2-Cl--C.sub.6 H.sub.4)furan-2-yl 1148 4-(3-Cl--C.sub.6 H.sub.4)furan-2-yl 1149 4-(4-Cl--C.sub.6 H.sub.4)furan-2-yl 1150 4-(2-Br--C.sub.6 H.sub.4)furan-2-yl 1151 4-(3-Br--C.sub.6 H.sub.4)furan-2-yl 1152 4-(4-Br--C.sub.6 H.sub.4)furan-2-yl 1153 4-(2-F-C.sub.6 H.sub.4)furan-2-yl 1154 4-(3-F-C.sub.6 H.sub.4)furan-2-yl 1155 4-(4-F-C.sub.6 H.sub.4)furan-2-yl 1156 4-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1157 4-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1158 4-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1159 4-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1160 4-(2,4-F.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1161 4-(2,5-F.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1162 4-(2,6-F.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1163 4-(3,4-F.sub.2 --C.sub.6 H.sub.3)furan-2-yl 1164 4-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)furan-2-yl 1165 4-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)furan-2-yl 1166 4-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)furan-2-yl 1167 4-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)furan-2-yl 1168 4-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]furan-2-yl 1169 5-CH(CH.sub.3).sub.2 -thien-2-yl 1170 5-C(CH.sub.3).sub.3 -thien-2-yl 1171 5-cyclopropylthien-2-yl 1172 5-C.sub.6 H.sub.5 -thien-2-yl 1173 5-(2-CH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1174 5-(3-CH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1175 5-(4-CH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1176 5-(3-OCH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1177 5-(4-OCH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1178 5-(4-NO.sub.2 --C.sub.6 H.sub.4)thien-2-yl 1179 5-(3-NO.sub.2 --C.sub.6 H.sub.4)thien-2-yl 1180 5-(4-CN--C.sub.6 H.sub.4)thien-2-yl 1181 5-(3-CN--C.sub.6 H.sub.4)thien-2-yl 1182 5-(3-CF.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1183 5-(4-CF.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1184 5-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)thien-2-yl 1185 5-(2-Cl--C.sub.6 H.sub.4)thien-2-yl 1186 5-(3-Cl--C.sub.6 H.sub.4)thien-2-yl 1187 5-(4-Cl--C.sub.6 H.sub.4)thien-2-yl 1188 5-(2-Br--C.sub.6 H.sub.4)thien-2-yl 1189 5-(3-Br--C.sub.6 H.sub.4)thien-2-yl 1190 5-(4-Br--C.sub.6 H.sub.4)thien-2-yl 1191 5-(2-F--C.sub.6 H.sub.4)thien-2-yl 1192 5-(3-F--C.sub.6 H.sub.4)thien-2-yl 1193 5-(4-F--C.sub.6 H.sub.4)thien-2-yl 1194 5-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1195 5-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1196 5-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1197 5-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1198 5-(2,4-F.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1199 5-(2,5-F.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1200 5-(2,6-F.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1201 5-(3,4-F.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1202 5-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)thien-2-yl 1203 5-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)thien-2-yl 1204 5-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)thien-2-yl 1205 5-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)thien-2-yl 1206 5-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]thien-2-yl 1207 4-CH(CH.sub.3).sub.2 -thien-2-yl 1208 4-C(CH.sub.3).sub.3 -thien-2-yl 1209 4-cyclopropylthien-2-yl 1210 4-C.sub.6 H.sub.5 -thien-2-yl 1211 4-(2-CH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1212 4-(3-CH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1213 4-(4-CH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1214 4-(3-OCH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1215 4-(4-OCH.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1216 4-(4-NO.sub.2 --C.sub.6 H.sub.4)thien-2-yl 1217 4-(3-NO.sub.2 --C.sub.6 H.sub.4)thien-2-yl 1218 4-(4-CN--C.sub.6 H.sub.4)thien-2-yl 1219 4-(3-CN--C.sub.6 H.sub.4)thien-2-yl 1220 4-(3-CF.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1221 4-(4-CF.sub.3 --C.sub.6 H.sub.4)thien-2-yl 1222 4-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)thien-2-yl 1223 4-(2-Cl--C.sub.6 H.sub.4)thien-2-yl 1224 4-(3-Cl--C.sub.6 H.sub.4)thien-2-yl 1225 4-(4-Cl--C.sub.6 H.sub.4)thien-2-yl 1226 4-(2-Br--C.sub.6 H.sub.4)thien-2-yl 1227 4-(3-Br--C.sub.6 H.sub.4)thien-2-yl 1228 4-(4-Br--C.sub.6 H.sub.4)thien-2-yl 1229 4-(2-F--C.sub.6 H.sub.4)thien-2-yl 1230 4-(3-F--C.sub.6 H.sub.4)thien-2-yl 1231 4-(4-F--C.sub.6 H.sub.4)thien-2-yl 1232 4-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1233 4-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1234 4-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1235 4-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1236 4-(2,4-F.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1237 4-(2,5-F.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1238 4-(2,6-F.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1239 4-(3,4-F.sub.2 --C.sub.6 H.sub.3)thien-2-yl 1240 4-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)thien-2-yl 1241 4-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)thien-2-yl 1242 4-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)thien-2-yl 1243 4-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)thien-2-yl 1244 4-[2,5-(CH.sub.3 ).sub.2 --C.sub.6 H.sub.3 ]thien-2-yl 1245 2-CH.sub.3 -thien-4-yl 1246 2-CH(CH.sub.3).sub.2 -thien-4-yl 1247 2-C(CH.sub.3).sub.3 -thien-4-yl 1248 2-cyclopropylthien-4-yl 1249 2-C.sub.6 H.sub.5 -thien-4-yl 1250 2-(2-CH.sub.3 --C.sub.6 H.sub.4)thien-4-yl 1251 2-(3-CH.sub.3 --C.sub.6 H.sub.4)thien-4-yl 1252 2-(4-CH.sub.3 --C.sub.6 H.sub.4)thien-4-yl 1253 2-(3-OCH.sub.3 --C.sub.6 H.sub.4)thien-4-yl 1254 2-(4-OCH.sub.3 --C.sub.6 H.sub.4)thien-4-yl 1255 2-(4-NO.sub.2 --C.sub.6 H.sub.4)thien-4-yl 1256 2-(3-NO.sub.2 --C.sub.6 H.sub.4)thien-4-yl 1257 2-(4-CN--C.sub.6 H.sub.4)thien-4-yl 1258 2-(3-CN--C.sub.6 H.sub.4)thien-4-yl 1259 2-(3-CF.sub.3 --C.sub.6 H.sub.4)thien-4-yl 1260 2-(4-CF.sub.3 --C.sub.6 H.sub.4)thien-4-yl 1261 2-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)thien-4-yl 1262 2-(2-Cl--C.sub.6 H.sub.4)thien-4-yl 1263 2-(3-Cl--C.sub.6 H.sub.4)thien-4-yl 1264 2-(4-Cl--C.sub.6 H.sub.4)thien-4-yl 1265 2-(2-Br--C.sub.6 H.sub.4)thien-4-yl 1266 2-(3-Br--C.sub.6 H.sub.4)thien-4-yl 1267 2-(4-Br--C.sub.6 H.sub.4)thien-4-yl 1268 2-(2-F--C.sub.6 H.sub.4)thien-4-yl 1269 2-(3-F--C.sub.6 H.sub.4)thien-4-yl 1270 2-(4-F--C.sub.6 H.sub.4)thien-4-yl 1271 2-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)thien-4-yl 1272 2-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)thien-4-yl 1273 2-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)thien-4-yl 1274 2-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)thien-4-yl 1275 2-(2,4-F.sub.2 --C.sub.6 H.sub.3)thien-4-yl 1276 2-(2,5-F.sub.2 --C.sub.6 H.sub.3)thien-4-yl 1277 2-(2,6-F.sub.2 --C.sub.6 H.sub.3)thien-4-yl 1278 2-(3,4-F.sub.2 --C.sub.6 H.sub.3)thien-4-yl 1279 2-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)thien-4-yl 1280 2-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)thien-4-yl 1281 2-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)thien-4-yl 1282 2-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)thien-4-yl 1283 2-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]thien-4-yl 1284 1-CH(CH.sub.3).sub.2 -pyrazol-4-yl 1285 1-C(CH.sub.3).sub.3 -pyrazol-4-yl 1286 1-cyclopropylpyrazol-4-yl 1287 1-C.sub.6 H.sub.5 -pyrazol-4-yl 1288 1-(2-CH.sub.3 --C.sub.6 H.sub.4)pyrazol-4-yl 1289 1-(3-CH.sub.3 --C.sub.6 H.sub.4)pyrazol-4-yl 1290 1-(4-CH.sub.3 --C.sub.6 H.sub.4)pyrazol-4-yl 1291 1-(3-OCH.sub.3 --C.sub.6 H.sub.4)pyrazol-4-yl 1292 1-(4-OCH.sub.3 --C.sub.6 H.sub.4)pyrazol-4-yl 1293 1-(4-NO.sub.2 --C.sub.6 H.sub.4)pyrazol-4-yl 1294 1-(3-NO.sub.2 --C.sub.6 H.sub.4)pyrazol-4-yl 1295 1-(4-CN--C.sub.6 H.sub.4)pyrozol-4-yl 1296 1-(3-CN--C.sub.6 H.sub.4)pyrazol-4-yl 1297 1-(3-CF.sub.3 --C.sub.6 H.sub.4)pyrazol-4-yl 1298 1-(4-CF.sub.3 --C.sub.6 H.sub.4)pyrazol-4-yl 1299 1-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)pyrazol-4-yl 1300 1-(2-Cl--C.sub.6 H.sub.4)pyrazol-4-yl 1301 1-(3-Cl--C.sub.6 H.sub.4)pyrazol-4-yl 1302 1-(4-Cl--C.sub.6 H.sub.4)pyrazol-4-yl 1303 1-(2-Br--C.sub.6 H.sub.4)pyrazol-4-yl 1304 1-(3-Br--C.sub.6 H.sub.4)pyrazol-4-yl 1305 1-(4-Br--C.sub.6 H.sub.4)pyrazol-4-yl 1306 1-(2-F--C.sub.6 H.sub.4)pyrazol-4-yl 1307 1-(3-F--C.sub.6 H.sub.4)pyrazol-4-yl 1308 1-(4-F--C.sub.6 H.sub.4)pyrazol-4-yl 1309 1-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)pyrazol-4-yl 1310 1-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)pyrazol-4-yl 1311 1-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)pyrazol-4-yl 1312 1-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)pyrazol-4-yl 1313 1-(2,4-F.sub.2 --C.sub.6 H.sub.3)pyrazol-4-yl 1314 1-(2,5-F.sub.2 --C.sub.6 H.sub.3)pyrazol-4-yl 1315 1-(2,6-F.sub.2 --C.sub.6 H.sub.3)pyrazol-4-yl 1316 1-(3,4-F.sub.2 --C.sub.6 H.sub.3)pyrazol-4-yl 1317 1-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)pyrazol-4-yl 1318 1-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)pyrazol-4-yl 1319 1-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)pyrazol-4-yl 1320 1-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)pyrazol-4-yl 1321 1-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]pyrazol-4-yl 1322 1-CH(CH.sub.3).sub.2 -pyrazol-3-yl 1323 1-C(CH.sub.3).sub.3 -pyrazol-3-yl 1324 1-cyclopropylpyrazol-3-yl 1325 1-C.sub.6 H.sub.5 -pyrazol-3-yl 1326 1-(2-CH.sub.3 --C.sub.6 H.sub.4)pyrazol-3-yl 1327 1-(3-CH.sub.3 --C.sub.6 H.sub.4)pyrazol-3-yl 1328 1-(4-CH.sub.3 --C.sub.6 H.sub.4)pyrazol-3-yl 1329 1-(3-OCH.sub.3 --C.sub.6 H.sub.4)pyrazol-3-yl 1330 1-(4-OCH.sub.3 --C.sub.6 H.sub.4)pyrazol-3-yl 1331 1-(4-NO.sub.2 --C.sub.6 H.sub.4)pyrazol-3-yl 1332 1-(3-NO.sub.2 --C.sub.6 H.sub.4)pyrazol-3-yl 1333 1-(4-CN--C.sub.6 H.sub.4)pyrazol-3-yl 1334 1-(3-CN--C.sub.6 H.sub.4)pyrazol-3-yl 1335 1-(3-CF.sub.3 --C.sub.6 H.sub.4)pyrazol-3-yl 1336 1-(4-CF.sub.3 --C.sub.6 H.sub.4)pyrazol-3-yl 1337 1-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)pyrazol-3-yl 1338 1-(2-Cl--C.sub.6 H.sub.4)pyrazol-3-yl 1339 1-(3-Cl--C.sub.6 H.sub.4)pyrazol-3-yl 1340 1-(4-Cl--C.sub.6 H.sub.4)pyrazol-3-yl 1341 1-(2-Br--C.sub.6 H.sub.4)pyrazol-3-yl 1342 1-(3-Br--C.sub.6 H.sub.4)pyrazol-3-yl 1343 1-(4-Br--C.sub.6 H.sub.4)pyrazol-3-yl 1344 1-(2-F--C.sub.6 H.sub.4)pyrazol-3-yl 1345 1-(3-F--C.sub.6 H.sub.4)pyrazol-3-yl 1346 1-(4-F--C.sub.6 H.sub.4)pyrazol-3-yl 1347 1-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1348 1-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1349 1-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1350 1-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1351 1-(2,4-F.sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1352 1-(2,5-F.sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1353 1-(2,6-F.sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1354 1-(3,4-F.sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1355 1-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)pyrazol-3-yl 1356 1-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)pyrazol-3-yl 1357 1-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)pyrazol-3-yl 1358 1-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)pyrazol-3-yl 1359 1-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3)pyrazol-3-yl 1360 3-CH(CH.sub.3).sub.2 -isoxazol-5-yl 1361 3-C(CH.sub.3).sub.3 -isoxazol-5-yl 1362 3-cyclopropylisoxazol-5-yl 1363 3-C.sub.6 H.sub.5 -isoxazol-5-yl 1364 3-(2-CH.sub.3 --C.sub.6 H.sub.4)isoxazol-5-yl 1365 3-(3-CH.sub.3 --C.sub.6 H.sub.4)isoxazol-5-yl 1366 3-(4-CH.sub.3 --C.sub.6 H.sub.4)isoxazol-5-yl 1367 3-(3-OCH.sub.3 --C.sub.6 H.sub.4)isoxazol-5-yl 1368 3-(4-OCH.sub.3 --C.sub.6 H.sub.4)isoxazol-5-yl 1369 3-(4-NO.sub.2 --C.sub.6 H.sub.4)isoxazol-5-yl 1370 3-(3-NO.sub.2 --C.sub.6 H.sub.4)isoxazol-5-yl 1371 3-(4-CN--C.sub.6 H.sub.4)isoxazol-5-yl 1372 3-(3-CN--C.sub.6 H.sub.4)isoxazol-5-yl 1373 3-(3-CF.sub.3 --C.sub.6 H.sub.4)isoxazol-5-yl 1374 3-(4-CF.sub.3 --C.sub.6 H.sub.4)isoxazol-5-yl 1375 3-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)isoxazol-5-yl 1376 3-(2-Cl--C.sub.6 H.sub.4)isoxazol-5-yl 1377 3-(3-Cl--C.sub.6 H.sub.4)isoxazol-5-yl 1378 3-(4-Cl--C.sub.6 H.sub.4)isoxazol-5-yl 1379 3-(2-Br--C.sub.6 H.sub.4)isoxazol-5-yl 1380 3-(3-Br--C.sub.6 H.sub.4)isoxazol-5-yl 1381 3-(4-Br--C.sub.6 H.sub.4)isoxazol-5-yl 1382 3-(2-F--C.sub.6 H.sub.4)isoxazol-5-yl 1383 3-(3-F--C.sub.6 H.sub.4)isoxazol-5-yl 1384 3-(4-F--C.sub.6 H.sub.4)isoxazol-5-yl 1385 3-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)isoxazol-5-yl 1386 3-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)isoxazol-5-yl 1387 3-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)isoxazol-5-yl 1388 3-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)isoxazol-5-yl 1389 3-(2,4-F.sub.2 --C.sub.6 H.sub.3)isoxazol-5-yl 1390 3-(2,5-F.sub.2 --C.sub.6 H.sub.3)isoxazol-5-yl 1391 3-(2,6-F.sub.2 --C.sub.6 H.sub.3)isoxazol-5-yl 1392 3-(3,4-F.sub.2 --C.sub.6 H.sub.3)isoxazol-5-yl 1393 3-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)isoxazol-5-yl 1394 3-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)isoxazol-5-yl 1395 3-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)isoxazol-5-yl 1396 3-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)isoxazol-5-yl 1397 3-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]isoxazol-5-yl 1398 5-CH(CH.sub.3).sub.2 -isoxazol-3-yl 1399 5-C(CH.sub.3).sub.3 -isoxazol-3-yl 1400 5-cyclopropylisoxazol-3-yl 1401 5-C.sub.6 H.sub.5 -isoxazol-3-yl 1402 5-(2-CH.sub.3 --C.sub.6 H.sub.4)isoxazol-3-yl 1403 5-(3-CH.sub.3 --C.sub.6 H.sub.4)isoxazol-3-yl 1404 5-(4-CH.sub.3 --C.sub.6 H.sub.4)isoxazol-3-yl 1405 5-(3-OCH.sub.3 --C.sub.6 H.sub.4)isoxazol-3-yl 1406 5-(4-OCH.sub.3 --C.sub.6 H.sub.4)isoxazol-3-yl 1407 5-(4-NO.sub.2 --C.sub.6 H.sub.4)isoxazol-3-yl 1408 5-(3-NO.sub.2 --C.sub.6 H.sub.4)isoxazol-3-yl 1409 5-(4-CN--C.sub.6 H.sub.4)isoxazol-3-yl 1410 5-(3-CN--C.sub.6 H.sub.4)isoxazol-3-yl 1411 5-(3-CF.sub.3 --C.sub.6 H.sub.4)isoxazol-3-yl 1412 5-(4-CF.sub.3 --C.sub.6 H.sub.4)isoxazol-3-yl 1413 5-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)isoxazol-3-yl 1414 5-(2-Cl--C.sub.6 H.sub.4)isoxazol-3-yl 1415 5-(3-Cl--C.sub.6 H.sub.4)isoxazol-3-yl 1416 5-(4-Cl--C.sub.6 H.sub.4)isoxazol-3-yl 1417 5-(2-Br--C.sub.6 H.sub.4)isoxazol-3-yl 1418 5-(3-Br--C.sub.6 H.sub.4)isoxazol-3-yl 1419 5-(4-Br--C.sub.6 H.sub.4)isoxazol-3-yl 1420 5-(2-F--C.sub.6 H.sub.4)isoxazol-3-yl 1421 5-(3-F--C.sub.6 H.sub.4)isoxazol-3-yl 1422 5-(4-F--C.sub.6 H.sub.4)isoxazol-3-yl 1423 5-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)isoxazol-3-yl 1424 5-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)isoxazol-3-yl 1425 5-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)isoxazol-3-yl 1426 5-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)isoxazol-3-yl 1427 5-(2,4-F.sub.2 --C.sub.6 H.sub.3)isoxazol-3-yl 1428 5-(2,5-F.sub.2 --C.sub.6 H.sub.3)isoxazol-3-yl 1429 5-(2,6-F.sub.2 --C.sub.6 H.sub.3)isoxazol-3-yl 1430 5-(3,4-F.sub.2 --C.sub.6 H.sub.3)isoxazol-3-yl 1431 5-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)isoxazol-3-yl 1432 5-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)isoxazol-3-yl 1433 5-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)isoxazol-3-yl 1434 5-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)isoxazol-3-yl 1435 5-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]isoxazol-3-yl 1436 3-CH(CH.sub.3).sub.2 -isothiazol-5-yl 1437 3-C(CH.sub.3).sub.3 -isothiazol-5-yl 1438 3-cyclopropylisothiazol-5-yl 1439 3-C.sub.6 H.sub.5 -isothiazol-5-yl 1440 3-(2-CH.sub.3 --C.sub.6 H.sub.4)isothiazol-5-yl 1441 3-(3-CH.sub.3 --C.sub.6 H.sub.4)isothiazol-5-yl 1442 3-(4-CH.sub.3 --C.sub.6 H.sub.4)isothiazol-5-yl 1443 3-(3-OCH.sub.3 --C.sub.6 H.sub.4)isothiazol-5-yl 1444 3-(4-OCH.sub.3 --C.sub.6 H.sub.4)isothiazol-5-yl 1445 3-(4-NO.sub.2 --C.sub.6 H.sub.4)isothiazol-5-yl 1446 3-(3-NO.sub.2 --C.sub.6 H.sub.4)isothiazol-5-yl 1447 3-(4-CN--C.sub.6 H.sub.4)isothiazol-5-yl 1448 3-(3-CN--C.sub.6 H.sub.4)isothiazol-5-yl 1449 3-(3-CF.sub.3 --C.sub.6 H.sub.4)isothiazol-5-yl 1450 3-(4-CF.sub.3 --C.sub.6 H.sub.4)isothiazol-5-yl 1451 3-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)isothiazol-5-yl 1452 3-(2-Cl--C.sub.6 H.sub.4)isothiazol-5-yl 1453 3-(3-Cl--C.sub.6 H.sub.4)isothiazol-5-yl 1454 3-(4-Cl--C.sub.6 H.sub.4)isothiazol-5-yl 1455 3-(2-Br--C.sub.6 H.sub.4)isothiazol-5-yl 1456 3-(3-Br--C.sub.6 H.sub.4)isothiazol-5-yl 1457 3-(4-Br--C.sub.6 H.sub.4)isothiazol-5-yl 1458 3-(2-F--C.sub.6 H.sub.4)isothiazol-5-yl 1459 3-(3-F--C.sub.6 H.sub.4)isothiazol-5-yl 1460 3-(4-F--C.sub.6 H.sub.4)isothiazol-5-yl 1461 3-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)isothiazol-5-yl 1462 3-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)isothiazol-5-yl 1463 3-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)isothiazol-5-yl 1464 3-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)isothiazol-5-yl 1465 3-(2,4-F.sub.2 --C.sub.6 H.sub.3)isothiazol-5-yl 1466 3-(2,5-F.sub.2 --C.sub.6 H.sub.3)isothiazol-5-yl 1467 3-(2,6-F.sub.2 --C.sub.6 H.sub.3)isothiazol-5-yl 1468 3-(3,4-F.sub.2 --C.sub.6 H.sub.3)isothiazol-5-yl 1469 3-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)isothiazol-5-yl 1470 3-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)isothiazol-5-yl 1471 3-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)isothiazol-5-yl 1472 3-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)isothiazol-5-yl 1473 3-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]isothiazol-5-yl 1474 2-CH(CH.sub.3).sub.2 -oxazol-4-yl 1475 2-C(CH.sub.3).sub.3 -oxazol-4-yl 1476 2-cyclopropyloxazol-4-yl 1477 2-C.sub.6 H.sub.5 -oxazol-4-yl 1478 2-(2-CH.sub.3 --C.sub.6 H.sub.4)oxazol-4-yl 1479 2-(3-CH.sub.3 --C.sub.6 H.sub.4)oxazol-4-yl 1480 2-(4-CH.sub.3 --C.sub.6 H.sub.4)oxazol-4-yl 1481 2-(3-OCH.sub.3 --C.sub.6 H.sub.4)oxazol-4-yl 1482 2-(4-OCH.sub.3 --C.sub.6 H.sub.4)oxazol-4-yl 1483 2-(4-NO.sub.2 --C.sub.6 H.sub.4)oxazol-4-yl 1484 2-(3-NO.sub.2 --C.sub.6 H.sub.4)oxazol-4-yl 1485 2-(4-CN--C.sub.6 H.sub.4)oxazol-4-yl 1486 2-(3-CN--C.sub.6 H.sub.4)oxazol-4-yl 1487 2-(3-CF.sub.3 --C.sub.6 H.sub.4)oxazol-4-yl 1488 2-(4-CF.sub.3 --C.sub.6 H.sub.4)oxazol-4-yl 1489 2-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)oxazol-4-yl 1490 2-(2-Cl--C.sub.6 H.sub.4)oxazol-4-yl 1491 2-(3-Cl--C.sub.6 H.sub.4)oxazol-4-yl 1492 2-(4-Cl--C.sub.6 H.sub.4)oxazol-4-yl 1493 2-(2-Br--C.sub.6 H.sub.4)oxazol-4-yl 1494 2-(3-Br--C.sub.6 H.sub.4)oxazol-4-yl 1495 2-(4-Br--C.sub.6 H.sub.4)oxazol-4-yl 1496 2-(2-F--C.sub.6 H.sub.4)oxazol-4-yl 1497 2-(3-F--C.sub.6 H.sub.4)oxazol-4-yl 1498 2-(4-F--C.sub.6 H.sub.4)oxazol-4-yl 1499 2-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)oxazol-4-yl 1500 2-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)oxazol-4-yl 1501 2-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)oxazol-4-yl 1502 2-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)oxazol-4-yl 1503 2-(2,4-F.sub.2 --C.sub.6 H.sub.3)oxazol-4-yl 1504 2-(2,5-F.sub.2 --C.sub.6 H.sub.3)oxazol-4-yl 1505 2-(2,6-F.sub.2 --C.sub.6 H.sub.3)oxazol-4-yl 1506 2-(3,4-F.sub.2 --C.sub.6 H.sub.3)oxazol-4-yl 1507 2-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)oxazol-4-yl 1508 1-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)oxazol-4-yl 1509 1-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)oxazol-4-yl 1510 2-(5-Cl, 2-CH.sub.3l --C.sub.6 H.sub.3)oxazol-4-yl 1511 2-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]oxazol-4-yl 1512 2-CH(CH.sub.3l ).sub.2 -thiazol-4-yl 1513 2-C(CH.sub.3).sub.2 -thiazol-4-yl 1514 2-cyclopropylthiazol-4-yl 1515 2-C.sub.6 H.sub.5 -thiazol-4-yl 1516 2-(2-CH.sub.3 --C.sub.6 H.sub.4)thiazol-4-yl 1517 2-(3-CH.sub.3 --C.sub.6 H.sub.4)thiazol-4-yl 1518 2-(4-CH.sub.3 --C.sub.6 H.sub.4)thiazol-4-yl 1519 2-(3-OCH.sub.3 --C.sub.6 H.sub.4)thiazol-4-yl 1520 2-(4-OCH.sub.3 --C.sub.6 H.sub.4)thiazol-4-yl 1521 2-(4-NO.sub.2 --C.sub.6 H.sub.4)thiazol-4-yl 1522 2-(3-NO.sub.2 --C.sub.6 H.sub.4)thiazol-4-yl 1523 2-(4-CN--C.sub.6 H.sub.4)thiazol-4-yl 1524 2-(3-CN--C.sub.6 H.sub.4)thiazol-4-yl 1525 2-(3-CF.sub.3 --C.sub.6 H.sub.4)thiazol-4-yl 1526 2-(4-CF.sub.3 --C.sub.6 H.sub.4)thiazol-4-yl 1527 2-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)thiazol-4-yl 1528 2-(2-Cl--C.sub.6 H.sub.4)thiazol-4-yl 1529 2-(3-Cl--C.sub.6 H.sub.4)thiazol-4-yl 1530 2-(4-Cl--C.sub.6 H.sub.4)thiazol-4-yl 1531 2-(2-Br--C.sub.6 H.sub.4)thiazol-4-yl 1532 2-(3-Br--C.sub.6 H.sub.4)thiazol-4-yl 1533 2-(4-Br--C.sub.6 H.sub.4)thiazol-4-yl 1534 2-(2-F--C.sub.6 H.sub.4)thiazol-4-yl 1535 2-(3-F--C.sub.6 H.sub.4)thiazol-4-yl 1536 2-(4-F--C.sub.6 H.sub.4)thiazol-4-yl 1537 2-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1538 2-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1539 2-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1540 2-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1541 2-(2,4-F.sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1542 2-(2,5-F.sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1543 2-(2,6-F.sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1544 2-(3,4-F.sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1545 2-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)thiazol-4-yl 1546 2-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)thiazol-4-yl 1547 2-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)thiazol-4-yl 1548 2-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)thiazol-4-yl 1549 2-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3)thiazol-4-yl 1550 1,3-(CH.sub.3).sub.2 -1,2,4-triazol-5-yl 1551 1-CH(CH.sub.3).sub.2 -1,2,4-triazol-3-yl 1552 1-C(CH.sub.3).sub.3 -1,2,4-triazol-3-yl 1553 1-cyclopropyl-1,2,4-triazol-3-yl 1554 1-C.sub.6 H.sub.5 -1,2,4-triazol-3-yl 1555 1-(2-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1556 1-(3-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1557 1-(4-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1558 1-(3-OCH.sub.3 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1559 1-(4-OCH.sub.3 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1560 1-(4-NO.sub.2 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1561 1-(3-NO.sub.2 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1562 1-(4-CN--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1563 1-(3-CN--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1564 1-(3-CF.sub.3 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1565 1-(4-CF.sub.3 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1566 1-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1567 1-(4-C.sub.6 H.sub.5 --C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1568 1-(2-Cl--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1569 1-(3-Cl--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1570 1-(4-Cl--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1571 1-(2-Br--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1572 1-(3-Br--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1573 1-(4-Br--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1574 1-(2-F--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1575 1-(3-F--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1576 1-(4-F--C.sub.6 H.sub.4)-1,2,4-triazol-3-yl 1577 1-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1578 1-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1579 1-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1580 1-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1581 1-(2,4-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1582 1-(2,5-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1583 1-(2,6-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1584 1-(3,4-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1585 1-(2-Cl, 5-OCH.sub.3 C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1586 1-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1587 1-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1588 1-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)-1,2,4-triazol-3-yl 1589 1-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]-1,2,4-triazol-3-yl 1590 5-C(CH.sub.3).sub.3 -1,3,4-oxadiazol-2-yl 1591 5-cyclopropyl-1,3,4-oxadiazol-2-yl 1592 5-C.sub.6 H.sub.5 -1,3,4-oxadiazol-2-yl 1593 5-(2-CH.sub.3 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1594 5-(3-CH.sub.3 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1595 5-(4-CH.sub.3 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1596 5-(3-OCH.sub.3 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1597 5-(4-OCH.sub.3 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1598 5-(4-NO.sub.2 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1599 5-(3-NO.sub.2 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1600 5-(4-CN--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1601 5-(3-CN--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1602 5-(3-CF.sub.3 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1603 5-(4-CF.sub.3 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1604 5-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1605 5-(2-Cl--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1606 5-(3-Cl--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1607 5-(4-Cl--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1608 5-(2-Br--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1609 5-(3-Br--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1610 5-(4-Br--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1611 5-(2-F--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1612 5-(3-F--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1613 5-(4-F--C.sub.6 H.sub.4)-1,3,4-oxadiazol-2-yl 1614 5-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1615 5-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1616 5-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1617 5-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1618 5-(2,4-F.sub.2 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1619 5-(2,5-F.sub.2 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1620 5-(2,6-F.sub.2 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1621 5-(3,4-F.sub.2 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1622 5-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1623 5-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-y l 1624 5-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-yl 1625 5-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)-1,3,4-oxadiazol-2-y l 1626 5-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]-1,3,4-oxadiazol-2-yl 1627 5-C(CH.sub.3).sub.3 -1,2,4-oxadiazol-3-yl 1628 5-cyclopropyl-1,2,4-oxadiazol-3-yl 1629 5-C.sub.6 H.sub.5 -1,2,4-oxadiazol-3-yl 1630 5-(2-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1631 5-(3-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1632 5-(4-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1633 5-(3-OCH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1634 5-(4-OCH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1635 5-(4-NO.sub.2 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1636 5-(3-NO.sub.2 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1637 5-(4-CN--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1638 5-(3-CN--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1639 5-(3-CF.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1640 5-(4-CF.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1641 5-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1642 5-(2-Cl--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1643 5-(3-Cl--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1644 5-(4-Cl--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1645 5-(2-Br--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1646 5-(3-Br--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1647 5-(4-Br--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1648 5-(2-F--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1649 5-(3-F--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1650 5-(4-F--C.sub.6 H.sub.4)-1,2,4-oxadiazol-3-yl 1651 5-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1652 5-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1653 5-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1654 5-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1655 5-(2,4-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1656 5-(2,5-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1657 5-(2,6-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1658 5-(3,4-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1659 5-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1660 5-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-y l 1661 5-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-yl 1662 5-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-3-y l 1663 5-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]-1,2,4-oxadiazol-3-yl 1664 3-CH.sub.3 -1,2,4-oxadiazol-5-yl 1665 3-CH(CH.sub.3).sub.2 -1,2,4-oxadiazol-5-yl 1666 3-C(CH.sub.3).sub.3 -1,2,4-oxadiazol-5-yl 1667 3-cyclopropyl-1,2,4-oxadiazol-5-yl 1668 3-C.sub.6 H.sub.5 -1,2,4-oxadiazol-5-yl 1669 3-(2-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1670 3-(3-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1671 3-(4-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1672 3-(3-OCH.sub.3 C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1673 3-(4-OCH.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1674 3-(4-NO.sub.2 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1675 3-(3-NO.sub.2 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1676 3-(4-CN--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1677 3-(3-CN--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1678 3-(3-CF.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1679 3-(4-CF.sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1680 3-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1681 3-(2-Cl--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1682 3-(3-Cl--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1683 3-(4-Cl--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1684 3-(2-Br--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1685 3-(3-Br--C.sub.6 H.sub.4)-1,2,4-oxadiazol-6-yl 1686 3-(4-Br--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1687 3-(2-F--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1688 3-(3-F--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1689 3-(4-F--C.sub.6 H.sub.4)-1,2,4-oxadiazol-5-yl 1690 3-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1691 3-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1692 3-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1693 3-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1694 3-(2,4-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1695 3-(2,5-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1696 3-(2,6-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1697 3-(3,4-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1698 3-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1699 3-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-y l 1700 3-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-yl 1701 3-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)-1,2,4-oxadiazol-5-y l 1702 3-[2,5-(CH.sub.3 ).sub.2 --C.sub.6 H.sub.3 ]-1,2,4-oxadiazol-5-yl 1703 5-CH.sub.3 -1,2,4-thiadiazol-3-yl 1704 5-CH(CH.sub.3 ).sub.2 -1,2,4-thiadiazol-3-yl 1705 5-C(CH.sub.3).sub.3 -1,2,4-thiadiazol-3-yl 1706 5-cyclopropyl-1,2,4-thiadiazol-3-yl 1707 5-C.sub.6 H.sub.5 -1,2,4-thiadiazol-3-yl 1708 5-(2-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1709 5-(3-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1710 5-(4-CH.sub.3 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1711 5-(3-OCH.sub.3 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1712 5-(4-OCH.sub.3 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1713 5-(4-NO.sub.2 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1714 5-(3-NO.sub.2 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1715 5-(4-CN--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1716 5-(3-CN--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1717 5-(3-CF.sub.3 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1718 5-(4-CF.sub.3 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1719 5-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1720 5-(2-Cl--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1721 5-(3-Cl--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1722 5-(4-Cl--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1723 5-(2-Br--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1724 5-(3-Br--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1725 5-(4-Br--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1726 5-(2-F--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1727 5-(3-F--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1728 5-(4-F--C.sub.6 H.sub.4)-1,2,4-thiadiazol-3-yl 1729 5-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1730 5-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1731 5-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1732 5-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1733 5-(2,4-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1734 5-(2,5-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1735 5-(2,6-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1736 5-(3,4-F.sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1737 5-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1738 5-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3- yl 1739 5-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1740 5-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3- yl 1741 5-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3)-1,2,4-thiadiazol-3-yl 1742 5-CH.sub.3 -1,3,4-thiadiazol-2-yl 1743 5-CH(CH.sub.3).sub.2 -1,3,4-thiadiazol-2-yl 1744 5-C(CH.sub.3).sub.3 -1,3,4-thiadiazol-2-yl 1745 5-cyclopropyl-1,3,4-thiadiazol-2-yl 1746 5-C.sub.6 H.sub.5 1,3,4-thiadiazol-2-yl 1747 5-(2-CH.sub.3 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1748 5-(3-CH.sub.3 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1749 5-(4-CH.sub.3 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1750 5-(3-OCH.sub.3 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1751 5-(4-OCH.sub.3 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1752 5-(4-NO.sub.2 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1753 5-(3-NO.sub.2 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1754 5-(4-CN--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1755 5-(3-CN--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1756 5-(3-CF.sub.3 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1757 5-(4-CF.sub.3 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1758 5-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1759 5-(2-Cl--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1760 5-(3-Cl--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1761 5-(4-Cl--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1762 5-(2-Br--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1763 5-(3-Br--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1764 5-(4-Br--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1765 5-(2-F--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1766 5-(3-F--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1767 5-(4-F--C.sub.6 H.sub.4)-1,3,4-thiadiazol-2-yl 1768 5-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1769 5-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1770 5-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1771 5-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1772 5-(2,4-F.sub.2 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1773 5-(2,5-F.sub.2 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1774 5-(2,6-F.sub.2 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1775 5-(3,4-F.sub.2 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1776 5-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1777 5-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2- yl 1778 5-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2-yl 1779 5-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)-1,3,4-thiadiazol-2- yl 1780 5-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]-1,3,4-thiadiazol-2-yl 1781 1-CH(CH.sub.3).sub.2 -imidazol-4-yl 1782 1-C(CH.sub.3).sub.3 -imidazol-4-yl 1783 1-cyclopropylimidazol-4-yl 1784 1-C.sub.6 H.sub.5 -imidazol-4-yl 1785 1-(2-CH.sub.3 --C.sub.6 H.sub.4)imidazol-4-yl 1786 1-(3-CH.sub.3 --C.sub.6 H.sub.4)imidazol-4-yl 1787 1-(4-CH.sub.3 --C.sub.6 H.sub.4)imidazol-4-yl 1788 1-(3-OCH.sub.3 --C.sub.6 H.sub.4)imidazol-4-yl 1789 1-(4-OCH.sub.3 --C.sub.6 H.sub.4)imidazol-4-yl 1790 1-(4-NO.sub.2 --C.sub.6 H.sub.4)imidazol-4-yl 1791 1-(3-NO.sub.2 --C.sub.6 H.sub.4)imidazol-4-yl 1792 1-(4-CN--C.sub.6 H.sub.4)imidazol-4-yl 1793 1-(3-CN--C.sub.6 H.sub.4)imidazol-4-yl 1794 1-(3-CF.sub.3 --C.sub.6 H.sub.4)imidazol-4-yl 1795 1-(4-CF.sub.3 --C.sub.6 H.sub.4)imidazol-4-yl 1796 1-(4-C(CH.sub.3).sub.3 --C.sub.6 H.sub.4)imidazol-4-yl 1797 1-(2-Cl--C.sub.6 H.sub.4)imidazol-4-yl 1798 1-(3-Cl--C.sub.6 H.sub.4)imidazol-4-yl 1799 1-(4-Cl--C.sub.6 H.sub.4)imidazol-4-yl 1800 1-(2-Br--C.sub.6 H.sub.4)imidazol-4-yl 1801 1-(3-Br--C.sub.6 H.sub.4)imidazol-4-yl 1802 1-(4-Br--C.sub.6 H.sub.4)imidazol-4-yl 1803 1-(2-F--C.sub.6 H.sub.4)imidazol-4-yl 1804 1-(3-F--C.sub.6 H.sub.4)imidazol-4-yl 1805 1-(4-F--C.sub.6 H.sub.4)imidazol-4-yl 1806 1-(2,4-Cl.sub.2 --C.sub.6 H.sub.3)imidazol-4-yl 1807 1-(2,5-Cl.sub.2 --C.sub.6 H.sub.3)imidazol-4-yl 1808 1-(2,6-Cl.sub.2 --C.sub.6 H.sub.3)imidazol-4-yl 1809 1-(3,4-Cl.sub.2 --C.sub.6 H.sub.3)imidazol-4-yl 1810 1-(2,4-F.sub.2 --C.sub.6 H.sub.3)imidazol-4-yl 1811 1-(2,5-F.sub.2 --C.sub.6 H.sub.3)imidazol-4-yl 1812 1-(2,6-F.sub.2 --C.sub.6 H.sub.3)imidazol-4-yl 1813 1-(3,4-F.sub.2 --C.sub.6 H.sub.3)imidazol-4-yl 1814 1-(2-Cl, 5-OCH.sub.3 --C.sub.6 H.sub.3)imidazol-4-yl 1815 1-(2-Cl, 5-CH.sub.3 --C.sub.6 H.sub.3)imidazol-4-yl 1816 1-(5-Cl, 2-OCH.sub.3 --C.sub.6 H.sub.3)imidazol-4-yl 1817 1-(5-Cl, 2-CH.sub.3 --C.sub.6 H.sub.3)imidazol-4-yl 1818 1-[2,5-(CH.sub.3).sub.2 --C.sub.6 H.sub.3 ]imidazol-4-yl______________________________________
The compounds I are suitable as fungicides.
The compounds I are distinguished by an outstanding activity against a broad spectrum of phytopathogenic fungi, in particular from the class of Ascomycetes, Deuteromycetes, Phycomycetes and Basidiomycetes. They are systemically active in some cases and can be employed as foliar and soil fungicides. They are of particular importance for the control of a multiplicity of fungi on various crop plants such as wheat, rye, barley, oats, bananas, rice, corn, grass, cotton, soybeans, coffee, sugar cane, grapes, fruit and decorative plants and vegetable plants such as cucumbers, beans, tomatoes, potatoes and cucurbits, and on the seeds of these plants.
They are specifically suitable for the control of the following plant diseases: Erysiphe graminis (powdery mildew) in cereals, Erysiphe cichoracearum and Sphaerotheca fuliginea on cucurbits, Podosphaera leucotricha on apples, Uncinula necator on vines, Puccinia species on cereals, Rhizoctonia species on cotton, rice and grass, Ustilago species on cereals and sugar cane, Venturia inaequalis (scab) on apples, Helminthosporium species on cereals, Septoria nodorum on wheat, Botrytis cinerea (gray mold) on strawberries, vines, vegetables and decorative plants, Cercospora arachidicola on groundnuts, Pseudocercosporella herpotrichoides on wheat, barley, Pyricularia oryzae on rice, Phytophthora infestans on potatoes and tomatoes, Fusarium and Verticillium species on various plants, Plasmopara viticola on vines, Pseudoperonospora species in hops and cucumbers, Alternaria species on vegetables and fruit and Mycosphaerella species in bananas.
The compounds I are applied by treating the fungi or the plants, seeds, materials or the soil to be protected from fungal attack with a fungicidally effective amount of the active compounds. They are applied before or after the infection of the materials, plants or seeds by the fungi.
Using formulation auxiliaries known per se, they can be converted into the customary formulations (compositions), such as solutions, emulsions, suspensions, dusts, powders, pastes and granules. The application form depends on the particular intended use; in each case it should guarantee a fine and uniform distribution of the compounds I. The formulations are prepared in a known manner, eg. by extending the active compound with solvents and/or carriers, if desired using emulsifiers and dispersants, it being possible in the case of water as a diluent also to use other organic solvents as auxiliary solvents. Suitable auxiliaries for this purpose are essentially: solvents such as aromatics (eg. xylene), chlorinated aromatics (eg. chlorobenzenes), paraffins (eg. petroleum fractions), alcohols (eg. methanol, butanol), ketones (eg. cyclohexanone), amines (eg. ethanolamine, dimethylformamide) and water; carriers such as ground natural minerals (eg. kaolins, argillaceous earths, talc, chalk) and ground synthetic minerals (eg. highly disperse silica, silicates); emulsifiers such as nonionic and anionic emulsifiers (eg. polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignin-sulfite waste liquors and methylcellulose.
The fungicidal compositions in general contain from 0.1 to 95, preferably from 0.5 to 90, % by weight of active compound.
Depending on the type of effect desired, the application rates are from 0.01 to 2.0 kg of active compound per ha.
In seed treatment, amounts of active compound of from 0.001 to 0.1 g, preferably 0.01 to 0.05 g, per kilogram of seed are in general needed.
The compositions according to the invention can also be present in the application form as fungicides together with other active compounds, eg. with herbicides, insecticides, growth regulators, fungicides or alternatively with fertilizers.
On mixing with fungicides, in many cases an increase in the fungicidal spectrum of action is obtained here.
The following list of fungicides with which the compounds according to the invention can be applied together is intended to illustrate the combination possibilities, but not restrict them:
sulfur, dithiocarbamates and their derivatives, such as ferric dimethyldithiocarbamate, zinc dimethyldithiocarbamate, zinc ethylenebisdithiocarbamate, manganese ethylenebisdithiocarbamate, manganese zinc ethylenediaminebisdithiocarbamate, tetramethylthiuram disulfide, ammonia complex of zinc (N,N-ethylenebisdithiocarbamate), ammonia complex of zinc (N,N'-propylenebisdithiocarbamate), zinc (N,N-propylenebisdithiocarbamate), N,N'-polypropylenebis(thiocarbamoyl) disulfide;
nitro derivatives, such as dinitro(1-methylheptyl)phenyl crotonate, 2-sec-butyl-4,6-dinitrophenyl 3,3-dimethylacrylate, 2-sec-butyl-4,6-dinitrophenyl isopropyl carbonate, diisopropyl 5-nitroisophthalate;
heterocyclic substances, such as 2-heptadecyl-2-imidazoline acetate, 2,4-dichloro-6-(o-chloroanilino) triazine, O,O-diethyl phthalimidophosphonothioate, 5-amino-1-[bis(dimethylamino)phosphinyl]-3-phenyl-1,2,4-triazole, 2,3-dicyano-1,4-dithioanthraquinone, 2-thio-1,3-dithiolo[4,5-b]quinoxaline, methyl 1-(butylcarbamoyl)-2-benzimidazolecarbamate, 2-ethoxycarbonylaminobenzimidazole, 2-(fur-2-yl)benzimidazole, 2-(thiazol-4-yl)benzimidazole, N-(1,1,2,2-tetrachloroethylthio)tetrahydrophthalimide, N-trichloromethylthiotetrahydrophthalimide, N-trichloromethylthiophthalimide;
N-dichlorofluoromethylthio-N',N'-dimethyl-N-phenylsulfamide, 5-ethoxy-3-trichloromethyl-1,2,3-thiadiazole, 2-thiocyanatomethylthiobenzothiazole, 1,4-dichloro-2,5-dimethoxybenzene, 4-(2-chlorophenylhydrazono)-3-methyl-5-isoxazolone, 2-thiopyridine-1-oxide, 8-hydroxyquinoline or its copper salt, 2,3-dihydro-5-carboxanilido-6-methyl-1,4-oxathiin, 2,3-dihydro-5-carboxanilido-6-methyl-1,4-oxathiin-4,4-dioxide, 2-methyl-5,6-dihydro-4H-pyran-3-carboxanilide, 2-methylfuran-3-carboxanilide, 2,5-dimethylfuran-3-carboxanilide, 2,4,5-trimethylfuran-3-carboxanilide, N-cyclohexyl-2,5-dimethylfuran-3-carboxamide, N-cyclohexyl-N-methoxy-2,5-dimethylfuran-3-carboxamide, 2-methylbenzanilide, 2-iodobenzanilide, N-formyl-N-morpholine-2,2,2-trichloroethyl acetal, piperazine-1,4-diylbis(1-(2,2,2-trichloroethyl))formamide, 1-(3,4-dichloroanilino)-1-formylamino-2,2,2-trichloroethane, 2,6-dimethyl-N-tridecylmorpholine or its salts, 2,6-dimethyl-N-cyclododecylmorpholine or its salts, N-[3-(p-tert-butylphenyl)-2-methylpropyl]-cis-2,6-dimethylmorpholine, N-[3-(p-tert-butylphenyl)-2-methylpropyl]piperidine, 1-[2-(2,4-dichlorophenyl)-4-ethyl-1,3-dioxolan-2-ylethyl]-1H-1,2,4-triazole, 1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-ylethyl]-1H-1,2,4-triazole, N-(n-propyl)-N-(2,4,6-trichlorophenoxyethyl)-N'-imidazolylurea, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanone, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol, .alpha.-(2-chlorophenyl)-.alpha.-(4-chlorophenyl)-5-pyrimidinemethanol, 5-butyl-2-dimethylamino-4-hydroxy-6-methylpyrimidine, bis(p-chlorophenyl)-3-pyridinemethanol, 1,2-bis(3-ethoxycarbonyl-2-thioureido)benzene, 1,2-bis(3-methoxycarbonyl-2-thioureido)benzene,
and various fungicides, such as dodecylguanidine acetate, 3-[3-(3,5-dimethyl-2-oxycyclohexyl)-2-hydroxyethyl]glutarimide, hexachlorobenzene, DL-methyl-N-(2,6-dimethylphenyl)-N-2-furoyl alaninate, DL-N-(2,6-dimethylphenyl)-N-(2'-methoxyacetyl)alanine methyl ester, N-(2,6-dimethylphenyl)-N-chloroacetyl-D,L-2-aminobutyrolactone, DL-N-(2,6-dimethylphenyl)-N-(phenylacetyl)alanine methyl ester, 5-methyl-5-vinyl-3-(3,5-dichlorophenyl)-2,4-dioxo-1,3-oxazolidine, 3-(3,5-dichlorophenyl)-5-methyl-5-methoxymethyl-1,3-oxazolidine-2,4-dione, 3-(3,5-dichlorophenyl)-1-isopropylcarbamoylhydantoin, N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboximide, 2-cyano-[N-ethylaminocarbonyl-2-methoximino]acetamide, 1-[2-(2,4-dichlorophenyl)pentyl]-1H-1,2,4-triazole, 2,4-difluoro-.alpha.-(1H-1,2,4-triazolyl-1-methyl)benzhydryl alcohol, N-(3-chloro-2,6-dinitro-4-trifluoromethylphenyl)-5-trifluoromethyl-3-chloro-2-aminopyridine, 1-((bis(4-fluorophenyl)methylsilyl)methyl)-1H-1,2,4-triazole;
strobilurins such as methyl E-methoximino[.alpha.-(o-tolyloxy)-o-tolyl]acetate, methyl E-2-{2-[6-(2-cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate, methyl E-methoximino-[.alpha.-(2-phenoxyphenyl)]acetamide, methyl E-methoximino-[.alpha.-(2,5-dimethylphenoxy)-o-tolyl]acetamide;
anilinopyrimidines such as N-(4,6-dimethylpyrimidin-2-yl)aniline, N-[4-methyl-6-(1-propynyl)pyrimidin-2-yl]aniline, N-(4-methyl-6-cyclopropylpyrimidin-2-yl)aniline;
phenylpyrroles such as 4-(2,2-difluoro-1,3-benzodioxol-4-yl)-pyrrole-3-carbonitrile, cinnamamides such as 3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acrylic acid morpholide;
(2RS,3SR)-1-[3-(2-chlorophenyl)-2-[4-fluorophenyl)oxiran-2-yl-methyl]-1H-1,2,4-triazole.
The compounds of the formula I are additionally suitable for controlling pests of the insects, arachnids and nematodes classes. They can be employed as pesticides in crop protection and in the hygiene, stored material protection and veterinary sectors.
The harmful insects include: from the order of the butterflies (Lepidoptera), for example, Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis virescens, Heliothis zea, Hellula undalis, Hibernia defoliaria, Hyphantria cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygma exigua, Leucoptera coffeella, Leucoptera scitella, Lithocolletis blancardella, Lobesia botrana, Loxostege sticticalis, Lymantria dispar, Lymantria monacha, Lyonetia clerkella, Malacosoma neustria, Mamestra brassicae, Orgyia pseudotsugata, Ostrinia nubilalis, Panolis flammea, Pectinophora gossypiella, Peridroma saucia, Phalera bucephala, Phthorimaea operculella, Phyllocnistis citrella, Pieris brassicae, Plathypena scabra, Plutella xylostella, Pseudoplusia includens, Rhyacionia frustrana, Scrobipalpula absoluta, Sitotroga cerealella, Sparganothis pilleriana, Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura, Thaumatopoea pityocampa, Tortrix viridana, Trichoplusia ni, Zeiraphera canadensis.
From the order of the beetles (Coleoptera), for example, Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Diabrotica longicornis, Diabrotica 12-punctata, Diabrotica virgifera, Epilachna varivestis, Epitrix hirtipennis, Eutinobothrus brasiliensis, Hylobius abietis, Hypera brunneipennis, Hypera postica, Ips typographus, Lema bilineata, Lema melanopus, Leptinotarsa decemlineata, Limonius californicus, Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus, Melolontha hippocastani, Melolontha melolontha, Oulema oryzae, Ortiorrhynchus sulcatus, Otiorrhynchus ovatus, Phaedon cochleariae, Phyllotreta chrysocephala, Phyllophaga sp., Phyllopertha horticola, Phyllotreta nemorum, Phyllotreta striolata, Popillia japonica, Sitona lineatus, Sitophilus granaria.
From the order of the dipterans (Diptera), for example, Aedes aegypti, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Ceratitis capitata, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Contarinia sorghicola, Cordylobia anthropophaga, Culex pipiens, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Fannia canicularis, Gasterophilus intestinalis, Glossina morsitans, Haematobia irritans, Haplodiplosis equestris, Hylemyya platura, Hypoderma lineata, Liriomyza sativae, Liriomyza trifolii, Lucilia caprina, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mayetiola destructor, Musca domestica, Muscina stabulans, Oestrus ovis, Oscinella frit, Pegomya hysocyami, Phorbia antiqua, Phorbia brassicae, Phorbia coarctata, Rhagoletis cerasi, Rhagoletis pomonella, Tabanus bovinus, Tipula oleracea, Tipula paludosa.
From the order of the thrips (Thysanoptera), for example, Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi, Thrips tabaci;
From the order of the hymenopterans (Hymenoptera), for example, Athalia rosae, Atta cephalotes, Atta sexdens, Atta texana, Hoplocampa minuta, Hoplocampa testudinea, Monomorium pharaonis, Solenopsis geminata, Solenopsis invicta.
From the order of the bugs (Heteroptera), for example, Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis, Thyanta perditor.
From the order of the plant-sucking insects (Homoptera), for example, Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis pomi, Aphis sambuci, Brachycaudus cardui, Brevicoryne brassicae, Cerosipha gossypii, Dreyfusia nordmannianae, Dreyfusia piceae, Dysaphis radicola, Dysaulacorthum pseudosolani, Empoasca fabae, Macrosiphum avenae, Macrosiphum euphorbiae, Macrosiphon rosae, Megoura viciae, Metopolophium dirhodum, Myzodes persicae, Myzus cerasi, Nilaparvata lugens, Pemphigus bursarius, Perkinsiella saccharicida, Phorodon humuli, Psylla mali, Psylla piri, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Sappaphis mala, Sappaphis mali, Schizaphis graminum, Schizoneura lanuginosa, Trialeurodes vaporariorum, Viteus vitifolii.
From the order of the termites (Isoptera), for example, Calotermes flavicollis, Leucotermes flavipes, Reticulitermes lucifugus, Termes natalensis.
From the order of the orthopterans (Orthoptera), for example, Acheta domestica, Blatta orientalis, Blattella germanica, Forficula auricularia, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femur-rubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Periplaneta americana, Schistocerca americana, Schistocerca peregrina, Stauronotus maroccanus, Tachycines asynamorus.
From the order of the Arachnoidea, for example, spiders (Acarina) such as Amblyomma americanum, Amblyomma variegatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Brevipalpus phoenicis, Bryobia praetiosa, Dermacentor silvarum, Eotetranychus carpini, Eriophyes sheldoni, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ornithodorus moubata, Otobius megnini, Paratetranychus pilosus, Dermanyssus gallinae, Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes ovis, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius, Tetranychus urticae.
From the class of the nematodes, for example, root gall nematodes, eg. Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica, cyst-forming nematodes, eg. Globodera rostochiensis, Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii, stem and leaf nematodes, eg. Belonolaimus longicaudatus, Ditylenchus destructor, Ditylenchus dipsaci, Heliocotylenchus multicinctus, Longidorus elongatus, Radopholus similis, Rotylenchus robustus, Trichodorus primitivus, Tylenchorhynchus claytoni, Tylenchorhynchus dubius, Pratylenchus neglectus, Pratylenchus penetrans, Pratylenchus curvitatus, Pratylenchus goodeyi.
The compounds I can be applied as such, in the form of their formulations (compositions) obtained using formulation auxiliaries known per se or the application forms prepared therefrom, eg. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dust compositions, scattering compositions or granules, by spraying, atomizing, dusting, scattering or watering. The application forms depend entirely on the intended uses; in each case they should if possible guarantee the finest distribution of the active compounds according to the invention.
The active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges.
In general, they are from 0.0001 to 10%, preferably from 0.01 to 1%.
The active compounds can also be used with good effect in the ultra-low volume method (ULV), it being possible to apply formulations containing more than 95% by weight of active compound or even the active compound without additives.
Under outdoor conditions, the application rate of active compound for controlling pests is from 0.1 to 2.0, preferably 0.2 to 1.0 kg/ha.
For the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions, mineral oil fractions of medium to high boiling point are suitable, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, eg. benzene, toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, strongly polar solvents, eg. dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone and water.
Aqueous application forms can be prepared from emulsion concentrates, pastes or wettable powders (wettable powders, oil dispersions) by addition of water. To prepare emulsions, pastes or oil dispersions, the substances can be homogenized in water as such or dissolved in an oil or solvent, by means of wetting agents, adherents, dispersants or emulsifiers. However, concentrates consisting of active substance, wetting agent, adherent, dispersant or emulsifier and possibly solvent or oil can also be prepared which are suitable for dilution with water.
Suitable surface-active substances are the alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid and dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkylsulfates, alkylsulfonates, fatty alcohol sulfates and fatty acids and also their alkali metal and alkaline earth metal salts, salts of sulfated fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensation products of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenyl ether, ethoxylated isooctylphenol, octylphenol or nonylphenol, alkylphenyl polyglycol ether, tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetate, sorbitol esters, lignosulfite waste liquors or methylcellulose.
Powder, scattering and dusting compositions can be prepared by mixing or joint grinding of the active substances with a solid carrier.
The formulations in general contain from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compound. The active compounds are employed here in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
Examples of formulations are:
I. 5 parts by weight of a compound I according to the invention are intimately mixed with 95 parts by weight of finely divided kaolin. In this way a dusting composition is obtained which contains 5% by weight of the active compound.
II. 30 parts by weight of a compound I according to the invention are intimately mixed with a mixture of 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil which has been sprayed onto the surface of this silica gel. In this manner a preparation of the active compound having good adherence is obtained (active compound content 23% by weight).
III. 10 parts by weight of a compound I according to the invention are dissolved in a mixture which consists of 90 parts by weight of xylene, 6 parts by weight of the addition product of from 8 to 10 mol of ethylene oxide to 1 mol of oleic acid N-monoethanolamide, 2 parts by weight of calcium salt of dodecylbenzenesulfonic acid and 2 parts by weight of the addition product of 40 mol of ethylene oxide to 1 mol of castor oil (active compound content 9% by weight).
IV. 20 parts by weight of a compound I according to the invention are dissolved in a mixture which consists of 60 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 5 parts by weight of the addition product of 7 mol of ethylene oxide to 1 mol of isooctylphenol and 5 parts by weight of the addition product of 40 mol of ethylene oxide to 1 mol of castor oil (active compound content 16% by weight).
V. 80 parts by weight of a compound I according to the invention are well mixed with 3 parts by weight of sodium salt of diisobutylnaphthalene-alpha-sulfonic acid, 10 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 7 parts by weight of powdered silica gel and the mixture is ground in a hammer mill (active compound content 80% by weight).
VI. 90 parts by weight of a compound I according to the invention are mixed with 10 parts by weight of N-methyl-.alpha.-pyrrolidone and a solution is obtained which is suitable for application in the form of very small drops (active compound content 90% by weight).
VII. 20 parts by weight of a compound I according to the invention are dissolved in a mixture which consists of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the addition product of 7 mol of ethylene oxide to 1 mol of isooctylphenol and 10 parts by weight of the addition product of 40 mol of ethylene oxide to 1 mol of castor oil. By pouring the solution into and finely dispersing it in 100,000 parts by weight of water, an aqueous dispersion is obtained which contains 0.02% by weight of the active compound.
VIII. 20 parts by weight of a compound I according to the invention are well mixed with 3 parts by weight of sodium salt of diisobutylnaphthalene-.alpha.-sulfonic acid, 17 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 60 parts by weight of powdered silica gel and the mixture is ground in a hammer mill. By finely dispersing the mixture in 20,000 parts by weight of water, a spray mixture is obtained which contains 0.1% by weight of the active compound.
Granules, eg. coated, impregnated and homogeneous granules, can be prepared by binding the active compounds to solid carriers.
Solid carriers are, for example, mineral earths, such as silicic acids, silica gels, silicates, talc, kaolin, attapulgous clay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as eg. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products, such as grain flour, tree bark, wood and nutshell meal, cellulose powder and other solid carriers.
Oils of various types, herbicides, fungicides, other pesticides and bactericides can be added to the active compounds, if desired only immediately before application (tank mix). These agents can be admixed with the agents according to the invention in a weight ratio from 1:10 to 10:1.

SYNTHESIS EXAMPLES
The chemical shifts (in ppm) of the .sup.1 H-NMR spectra were measured against tetramethylsilane (br=broad signal, s=singlet, d=doublet, m=multiplet).
EXAMPLE 1
Preparation of the compound S1 ##STR11##
9.2 g (0.03 mol) of methyl (E,E)-2-methoxyimino-2-(2'-[{1"-methyl,1"-acetyl}iminooxymethyl]phenyl)acetate (cf. WO-A 95/21153) were dissolved in 200 ml of tetrahydrofuran, treated with 50 ml of 40% strength by weight aqueous monomethylamine solution and allowed to stand at room temperature for 2 hours. The mixture was then treated with 2N hydrochloric acid, extracted with methyl tert-butyl ether, the organic phase was washed with water and dried over sodium sulfate, and the solvent was removed. As a residue, 7.7 g of (E,E)-2-methoxyimino-2-(2'-[{1"-methyl,1"-acetyl}iminooxymethyl]phenyl)acetic acid monomethylamide remained as colorless crystals of melting point 89-92.degree. C. A solution of 3.7 g (0.012 mol) of this compound in 50 ml of tetrahydrofuran was added to a solution of 2.4 g (0.048 mol) of hydrazine hydrate in 50 ml of tetrahydrofuran and the mixture was stirred at room temperature for 60 hours. It was then treated with water, extracted with methyl tert-butyl ether, the organic phase was washed with water and dried over sodium sulfate, and the solvent was removed. As a residue, 3.5 g of (E,E,E)-2-methoxyimino-2-(2'-[{1"-methyl,1"-{1'"-hydrazonoethyl}}iminooxymethyl]phenyl)acetic acid monomethylamide remained as a colorless oil.
1H-NMR (CDCl.sub.3): 1.89 (s, 3H); 1.99 (s, 3H); 2.9 (d, 3H); 3.94 (s, 3H); 5.05 (s, 2H); 5.44 (s, br, 2H); 6.71 (s, br, 1H); 7.15-7.47 (m, 4H).
1.6 g (0.005 mol) of this compound were dissolved in 100 ml of acetone. After addition of 1 drop of acetic acid, the reaction mixture was allowed to stand at room temperature for 60 hours. The acetone was then stripped off, the residue was taken up in methyl tert-butyl ether and water, the mixture was extracted with methyl tert-butyl ether and the organic phase was washed with water and dried over sodium sulfate. The solvent was then removed from the organic phase. As a residue, 1.7 g of the compound "S1" remained as a colorless oil.
.sup.1 H-NMR (CDCl.sub.3): 1.8 (s, 3H); 1.94 (s, 3H); 2.05 (s, 6H); 2.9 (d, 3H); 3.96 (s, 3H); 5.1 (s, 2H); 6.75 (s, br, 1H); 7.17-7.5 (m, 4H).
EXAMPLE 2
Preparation of the compound S2 ##STR12##
A solution of 20 g (0.11 mol) of 1-hydrazono-1-phenylpropan-2-one oxime [J. Med. Chem. 21 (1978), 623-8] in 300 ml of acetone was stirred at room temperature for 1 hour. After stripping off the solvent in a rotary evaporator, the residue was crystallized from methanol. 9.5 g (40% yield) of the compound S2 were thus obtained as colorless crystals of melting point 127-130.degree. C.
.sup.1 H-NMR (CDCl.sub.3): .delta.=1.87 (s,6H); 2.18 (s,3H); 6.98-7.36 (m,5H); 8.56 (s,br,1H).
EXAMPLE 3
Preparation of the compound S3 ##STR13##
2.5 g (11.5 mmol) of 1-(isopropylidenehydrazono)-1-phenylpropan-2-one oxime (compound S2), dissolved in 50 ml of dimethylformamide, were added to 0.29 g (12 mmol) of sodium hydride in 50 ml of dimethylformamide. The mixture was stirred for 30 min, then 3.3 g (11.5 mmol) of methyl (E)-3-methoxy-2-[(2'-bromomethyl)phenyl]acrylate were added and the reaction mixture was stirred at room temperature for 16 hours. It was poured onto water and extracted with tert-butyl methyl ether. The organic phase was washed with water, dried and concentrated. After column chromatography on silica gel (tert-butyl methyl ether/cyclohexane/2% triethylamine), 1.7 g (35% yield) of the compound S3 were obtained as a colorless oil.
IR (film): 2940, 1709, 1634, 1435, 1284, 1256, 1191, 1130, 1111, 1056, 1009 cm.sup.-1.
EXAMPLE 4
Preparation of the compound S4 ##STR14##
2.5 g (11.5 mmol) of 1-(isopropylidenehydrazono)-1-phenylpropan-2-one oxime (compound S2), dissolved in 50 ml of dimethylformamide, were added to 0.29 g (12 mmol) of sodium hydride in 50 ml of dimethylformamide. The mixture was stirred for 30 min, then 3.1 g (11.5 mmol) of methyl (E)-3-methyl-2-[(2'-bromomethyl)phenyl]acrylate were added and the reaction mixture was stirred at room temperature for 16 hours. It was poured onto water and extracted with tert-butyl methyl ether. The organic phase was washed with water, dried and concentrated. After column chromatography on silica gel (tert-butyl methyl ether/cyclohexane/2% triethylamine), 2.3 g (49% yield) of the compound S4 were obtained as a colorless oil.
.sup.1 H-NMR (CDCl.sub.3): .delta.=1.49 (d,3H); 1.89 (s,6H); 2.21 (s,3H); 3.64 (s,3H); 4.87-4.93 (m,2H); 6.98-7.36 (m,9H).
EXAMPLE 5
Preparation of the compound S5 ##STR15##
4.3 g (20 mmol) of 1-(isopropylidenehydrazono)-1-phenylpropan-2-one oxime (compound S2), dissolved in 50 ml of dimethylformamide, were added to 0.5 g (21 mmol) of sodium hydride in 50 ml of dimethylformamide. The mixture was stirred for 30 min, then 5.7 g (20 mmol) of methyl (E)-2-methoxyimino-2-[(2'-bromomethyl)phenyl]acetate were added and the reaction mixture was stirred at room temperature for 16 hours. It was poured onto water and extracted with tert-butyl methyl ether. The organic phase was washed with water, dried and concentrated. After column chromatography on silica gel (tert-butyl methyl ether/cyclohexane/2% triethylamine), 4.2 g (50% yield) of the compound S5 were obtained as a colorless oil.
.sup.1 H-NMR (CDCl.sub.3): .delta.=1.89 (s,6H); 2.17 (s,3H); 3.82 (s,3H); 3.97 (s,3H); 4.93 (s,2H); 7.00-7.40 (m,9H).
EXAMPLE 6
Preparation of the compound S6 ##STR16##
3.0 g (7.1 mmol) of the compound S5 were dissolved in 100 ml of tetrahydrofuran, treated with 20 ml of 40% strength aqueous monomethylamine solution and stirred at room temperature for 1 hour. The mixture was then treated with water, extracted with tert-butyl methyl ether and the organic phase was washed with water, dried over sodium sulfate and concentrated in a rotary evaporator. 3.0 g of the compound S6 were thus obtained as a colorless oil.
.sup.1 H-NMR (CDCl.sub.3): .delta.=1.89 (s,6H); 2.18 (s,3H); 2.85 (d,3H); 3.88 (s,3H); 4.94 (s,2H); 6.64 (s,br,1H); 6.98-7.38 (M,9H).
Compounds of the formula I can quite generally be prepared in a similar manner to that described above for the compounds S1 to S6.
Table I below shows the physical data of other prepared compounds according to the invention. The compounds S1, S3, S4, S5 and S6 are additionally included in the table.
TABLE 1__________________________________________________________________________ #STR17## -No. R.sup.1 Y X (R.sup.2).sub.m R.sup.3 R.sup.4 R.sup.5 R.sup.6 Data__________________________________________________________________________I.1 CH.sub.3 NH NOCH.sub.3 - (E) H CH.sub.3 CH.sub.3 CH.sub.3 CH.sub.3 see Example S1 I.2 CH.sub.3 NH NOCH.sub.3 - (E) H CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 H IR (film): 3340, 2930, 1673, 1614, 1525, 1448, 1362, 1038, 999, 979, 760, 695 cm.sup.-1 I.3 CH.sub.3 O NOCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 IR (film): 2940, 1727, 1443, 1437, 1218, 1199, 1069, 1048, 1018, 958, 698 cm.sup.-1 I.4 CH.sub.3 O CHOCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 .sup.1 H-NMR (CDCl.sub.3): .delta. = 0.93 ((t, 3H); 1.82 (s, 3H); 2.16 (q, 2H); 2.21 (s, 3H); 3.64 (s, 3H); 3.74 (s, 3H); 4.97 (s, 2H); 7.05-7.51 (m, 10H) ppm I.5 CH.sub.3 O NOCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 H .sup.1 H-NMR (CDCl.sub.3): .delta. = 1.94 and 1.85 (d, 3H); 2.15 and 2.18 (s, 3H); 3.82 and 3.79 (s, 3H); 3.97 and 4.0 (s, 3H); 4.85-5.12 (m, 2H); 7.0-7.83 (m, 10H) ppm I.6 CH.sub.3 NH NOCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 m.p. 75-78.degree. C. I.7 CH.sub.3 O CHCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 IR (film): 2960, 1717, 1143, 1435, 1364, 1252, 1208, 1036, 1010, 764, 696 cm.sup.-1 I.8 CH.sub.3 O NOCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 see Example S5 I.9 CH.sub.3 O CHOCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 see Example S3 I.10 CH.sub.3 O CHCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 see Example S4 I.11 CH.sub.3 NH NOCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 H .sup.1 H-NMR (CDCl.sub.3): .delta. = 1.95 and 1.86 (d, 3H); 2.16 and 2.19 (s, 3H); 2.87 and 2.78 (d, 3H); 3.89 and 3.92 (s, 3H); 4.86-5.09 (m, 2H); 6.62 and 6.83 (s, br, 1H); 7.0-7.88 (m, 10H) ppm I.12 CH.sub.3 NH NOCH.sub.3 - (E) H CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 see Example S6__________________________________________________________________________
USE EXAMPLES
1. Examples of action against harmful fungi: wheat mildew
Leaves of wheat seedlings of the variety "Fruhgold" grown in pots were sprayed until dripping wet using an aqueous spray mixture which was prepared using a stock solution of 10% active compound, 63% cyclohexanone and 27% emulsifier and dusted 24 hours after the spray coating had dried on with spores of wheat mildew (Erysiphe graminis var. tritici). The test plants ere then placed in a greenhouse at from 20 to 22.degree. C. and 75 to 80% relative atmospheric humidity. After 7 days, the extent of mildew development was assessed visually in % attack of the total leaf area.
______________________________________ % attack on the leaves after application of aqueous active compound preparation comprising Active compound 63 ppm of active compound______________________________________I.1 5 I.2 5 I.3 15 I.5 15 I.7 15 I.8 15 I.9 15 I.10 15 Comparison substance A 60 Compound 3.81 from Table 3 of WO 95/18 789 Untreated 75______________________________________
2. Examples of action against animal pests
It was possible to show the action of the compounds of the general formula I against animal pests by the following tests:
The active compounds were prepared
a) as a 0.1% strength solution in acetone or
b) as a 10% strength emulsion in a mixture of 70% by weight of cyclohexanone, 20% by weight of Nekanil.RTM. LN (Lutensol.RTM. AP6, wetting agent having emulsifier and dispersant action based on ethoxylated alkylphenols) and 10% by weight of Emulphor.RTM. EL (Emulan.RTM. EL, emulsifier based on ethoxylated fatty alcohols)
and diluted with acetone in the case of a) or with water in the case of b) according to the concentration desired.
After conclusion of the tests, the lowest concentration in each case was determined at which the compounds still produced an 80-100% inhibition or mortality in comparison with the untreated control tests (activity threshold or minimum concentration).

Azinooximethers, processes and intermediate products for manufacturing same, and the uses thereof in combating harmful fungi and pests

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