Derivatives of phenylacetic acid, their preparation and their use as pesticides

Abstract

Compounds of the formula I ##STR1## where n, W, X, Y, Z, R.sup.1, R.sup.2, and R.sup.3 are as defined herein exhibit fungicidal, insecticidal, and acaracidal activity.

Description

The present invention relates to novel phenylacetic acetic acid derivatives having fungicidal, insecticidal and acaricidal activity, fungicides containing these compounds and methods for controlling the fungi.

It is known (for example from European Patents 178,826, 253,213 and 280,185) that esters of acrylic acid, crotonic acid or methoxyiminoacetic acid can be used as fungicides. However, the action of these compounds is unsatisfactory in many cases.

We have found that novel phenylacetic acid derivatives of the general formula I have excellent fungicidal activity and in addition insecticidal and acaricidal activity. ##STR2##

In formula I,

n is 0 or 1, W may occupy any free position on the benzene ring and is hydrogen, halogen, such as fluorine, chlorine, bromine or iodine, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl or tert-butyl, unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy or tert-butoxy, preferably hydrogen, chlorine, methyl or methoxy, particularly preferably hydrogen, X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3 or CHC.sub.2 H.sub.5, Y is oxygen, sulfur or NR.sup.4, --O--NR.sup.4, --NR.sup.4 --O-- or NR.sup.4 --NR.sup.5, preferably oxygen, sulfur or NR.sup.4, particularly preferably oxygen or NR.sup.4, Z is oxygen, NR.sup.6, NOR.sup.7 or N--NR.sup.8 R.sup.9 or, if n is 1, furthermore sulfur, preferably oxygen or NOR.sup.7 or N--NR.sup.8 R.sup.9, particularly preferably oxygen or NOR.sup.7, R.sup.1 is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl as stated above, preferably hydrogen or methyl, particularly preferably hydrogen, R.sup.2 is independent of R.sup.1 and is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl as stated above, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl, unsubstituted or substituted and/or fused aryl, such as phenyl, naphthyl, anthryl or phenanthryl, unsubstituted or substituted and/or fused hetaryl, such as 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-quinolyl, 1-isoquinolyl, pyrazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 2-quinoxalinyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 2-furyl, 3-thienyl, 3-pyrazolyl, 5-pyrazolyl, 1-imidazolyl, 4-imidazolyl, 1,2,4-triazol-3-yl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 3-isoxazolyl, 2-thiazolyl, 4-isothiazolyl, 1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, 2-indolyl, 3-indolyl, 2-benzothiazolyl, 9-carbazolyl or 2-pteridinyl, C.sub.1 -C.sub.4 -perfluoroalkyl, such as trifluoromethyl, pentafluoroethyl, heptafluoroisopropyl or nonafluoro-n-butyl, or CO--V .

R.sup.2 is preferably hydrogen, C.sub.1 -C.sub.4 -alkyl or CO--V, particularly preferably hydrogen.

R.sup.3 is

hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl as stated above, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, such as ethenyl, propen-1-yl, propen-2-yl, propen-3-yl, 2-buten-1-yl or 2-methylpropen-1-yl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl as stated above, unsubstituted or substituted 3-membered to 6-membered heterocyclyl, such as oxiranyl, azetidinyl, tetrahydrofuran-2-yl, pyrrolidin-1-yl or thiopyran-4-yl, unsubstituted or substituted and/or fused aryl as stated above, unsubstituted or substituted and/or fused hetaryl as stated above, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, such as benzyl, 1-phenylethyl, 2-phenylethyl, 4-phenyl-n-butyl, 2-phenyl-2-methylprop-1-yl or naphthylmethyl, unsubstituted or substituted hetaryl-C.sub.1 -C.sub.4 -alkyl, such as pyrid-2-ylmethyl, 2-fur-3-ylethyl, 3-isoxazol-5-ylpropyl or 1-indolylmethyl, unsubstituted or substituted aryl-C.sub.2 -C.sub.4 -alkenyl, such as 1-phenylethenyl or 1-naphth-3-ylprop-1-en-3-yl, or unsubstituted or substituted hetaryl-C.sub.2 -C.sub.4 -alkenyl, such as 2-pyrid-4-ylethenyl or 1-thien-3-ylethenyl, or, if n is 0, furthermore cyano, C.sub.1 -C.sub.4 -perfluoroalkyl or unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl, such as ethynyl, propyn-1-yl, propyn-3-yl, 1-butyn-4-yl or 2-butyn-1-yl or, if n is 1 and Y is oxygen, furthermore unsubstituted or substituted trialkylsilyl, such as trimethylsilyl, triethylsilyl, tert-butyldimethylsilyl or di-tert-butylmethylsilyl.

R.sup.3 is preferably hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted and/or fused aryl, unsubstituted or substituted and/or fused hetaryl or unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl,

particularly preferably hydrogen, C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted phenyl or unsubstituted or substituted benzyl,

R.sup.4 and R.sup.5 are independent of one another and are each hydrogen,

unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl as stated above or unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl as stated above, preferably hydrogen, methyl or ethyl,

R.sup.6 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl as stated above or

unsubstituted or substituted and/or fused aryl or hetaryl as stated above, preferably substituted phenyl,

R.sup.7 and R.sup.8 are each

hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl as stated above, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl as stated above, unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl as stated above, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl as stated above, unsubstituted or substituted and/or fused aryl as stated above, unsubstituted or substituted and/or fused hetaryl as stated above, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl as stated above, unsubstituted or substituted hetaryl-C.sub.1 -C.sub.4 -alkyl as stated above, or COR.sup.10.

R.sup.7 is preferably hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted hetaryl-C.sub.1 -C.sub.4 -alkyl, particularly preferably C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted benzyl, and

R.sup.8 is preferably hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted aryl, particularly preferably unsubstituted or substituted phenyl, R.sup.9 has the same general and preferred meanings as R.sup.4 and is independent of R.sup.8,

R.sup.10 is

unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl as stated above, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl as stated above, unsubstituted or substituted aryl as stated above or unsubstituted or substituted hetaryl as stated above, preferably unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted aryl, particularly preferably methyl or unsubstituted or substituted phenyl,

V is

unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl as stated above, unsubstituted or substituted aryl as stated above, unsubstituted or substituted hetaryl as stated above, hydroxyl, unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy as stated above, unsubstituted or substituted allyloxy, unsubstituted or substituted benzyloxy or unsubstituted or substituted trimethylsilyloxy.

The bond between the two carbon atoms carrying R.sup.1 and R.sup.2 may be a single or a double bond. The double bond is preferred.

The radicals indicated as being unsubstituted or substituted can carry, in any position, one or more, preferably one to three, substituents, which are identical or different. These substituents are

hydrogen, halogen, cyano, nitro, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, haloalkyl, hydroxyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, aryloxy, heteroaryloxy, heterocyclyloxy, haloalkoxy, mercapto, alkylthio, alkenylthio, alkynylthio, cycloalkylthio, arylthio, heteroarylthio, heterocyclylthio, haloalkylthio, amino, alkylamino, alkenylamino, alkynylamino, cycloalkylamino, arylamino, heteroarylamino, heterocyclylamino, dialkylamino, N-alkyl-arylamino, N-alkyl-heteroarylamino, formyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, cycloalkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, heterocyclylcarbonyl, carboxyl, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, cycloalkyloxycarbonyl, aryloxycarbonyl, heteroaryloxycarbonyl, heterocyclyloxy-carbonyl, formyloxy, alkylcarbonyloxy, alkenylcarbonyloxy, alkynylcarbonyloxy, cycloalkylcarbonyloxy, arylcarbonyloxy, heteroarylcarbonyloxy, heterocyclylcarbonyloxy, aminocarbonyl, alkylaminocarbonyl, alkenyl-aminocarbonyl, alkynylaminocarbonyl, cycloalkylamino-carbonyl, arylaminocarbonyl, heteroarylaminocarbonyl, heterocyclylaminocarbonyl, dialkylaminocarbonyl, N-alkyl-arylaminocarbonyl, N-alkyl-heteroarylaminocarbonyl, hydroxylaminocarbonyl, alkoxyaminocarbonyl, alkenyloxyaminocarbonyl, alkynyloxyaminocarbonyl, formamido, alkyl-carbonylamino, alkenylcarbonylamino, alkynylcarbonyl-amino, cycloalkylcarbonylamino, arylcarbonylamino, heteroarylcarbonylamino, heterocyclylcarbonylamino, alkylcarbonyl-N-alkylamino, arylcarbonyl-N-alkylamino, heteroarylcarbonyl-N-alkylamino, aminothiocarbonyl, alkylamino-thiocarbonyl, dialkylaminothiocarbonyl, alkylsulfoxyl, arylsulfoxyl, heteroarylsulfoxyl, alkylsulfonyl, aryl-sulfonyl, heteroarylsulfonyl, hydroxysulfinyl, alkoxysulfinyl, hydroxysulfonyl, alkoxysulfonyl, alkylsulfinyloxy, arylsulfinyloxy, heteroarylsulfinyloxy, alkyl-sulfonyloxy, arylsulfonyloxy, heteroaryl sulfonyloxy, dialkoxyphosphinyl, bis(aryloxy)phosphinyl, trialkylsilyl, trialkylsilyloxy, or a fragment of the formula R'--O--N.dbd.CR", in which R' and R" independently of one another are hydrogen, alkyl, alkenyl or alkynyl and, is R' is not hydrogen, R" can also be alkoxy.

In the abovementioned substituents, halogen and the organic substructures, for example ethyl, each have the abovementioned meanings. The substituents can in turn be substituted by one or more of the abovementioned radicals.

The novel compounds of the formula I may be obtained in the preparation as mixtures of stereoisomers (E/Z isomers at C.dbd.C or C.dbd.N double bonds, diastereomers, enantiomers), which can be separated into their individual components in a conventional manner, for example by crystallization or chromatography. Both the individual isomers and the mixtures thereof can be used as fungicides, insecticides or acaricides, and the present invention relates to all of them. The fungicidal activity is preferred.

The present invention preferably relates to novel compounds of the general formula II ##STR3## where W may occupy any free position on the benzene ring and is hydrogen, chlorine, methyl or methoxy, preferably hydrogen,

X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3 or CHC.sub.2 H.sub.5, Z is oxygen, NR.sup.6, NOR.sup.7 or N--NR.sup.8 R.sup.9, preferably oxygen or NOR.sup.7, R.sup.1 and R.sup.2 are independent of one another and are each hydrogen or C.sub.1 -C.sub.4 -alkyl as stated above, preferably hydrogen, R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted 3-membered to 6-membered heterocyclyl, unsubstituted or substituted and/or fused aryl, unsubstituted or substituted and/or fused hetaryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted hetaryl-C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted aryl-C.sub.2 -C.sub.4 -alkenyl or unsubstituted or substituted hetaryl-C.sub.2 -C.sub.4 -alkenyl, in each case as stated above, preferably hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted aryl, unsubstituted or substituted hetaryl, particularly preferably C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted phenyl, R.sup.4 is hydrogen unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, in each case as stated above, preferably hydrogen, methyl or ethyl, R.sup.6 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted and/or fused aryl or hetaryl, in each case as stated above, preferably unsubstituted or substituted phenyl, R.sup.7 and R.sup.8 are each hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted and/or fused aryl, unsubstituted or substituted and/or fused hetaryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted hetaryl-C.sub.1 -C.sub.4 -alkyl, in each case as stated above, or COR.sup.10, R.sup.7 preferably being hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, or unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, particularly preferably C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted benzyl, and R.sup.8 preferably being unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, particularly preferably C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted benzyl, R.sup.9 has the same general and preferred meanings as R.sup.4 and is independent of R.sup.8 and R.sup.10 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted aryl or unsubstituted or substituted hetaryl, in each case as stated above, preferably C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted phenyl.

The present invention furthermore preferably relates to novel compounds of the general formula III ##STR4## where W may occupy any free position on the benzene ring and is hydrogen, chlorine, methyl or methoxy, preferably hydrogen,

X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3 or CHC.sub.2 H.sub.5, Y is oxygen, sulfur or NR.sup.4, preferably oxygen or NR.sup.4, R.sup.1 is hydrogen or C.sub.1 -C.sub.4 -alkyl, preferably hydrogen, R.sup.2 is hydrogen, C.sub.1 -C.sub.4 -alkyl or CO--V, preferably hydrogen, R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.1 -C.sub.4 -alkenyl, unsubstituted or substituted and/or fused aryl, unsubstituted or substituted and/or fused hetaryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted hetaryl-C.sub.1 -C.sub.4 -alkyl or, if Y is oxygen, furthermore trialkylsilyl, in each case as stated above, preferably C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted phenyl or unsubstituted or substituted benzyl, R.sup.4 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, in each case as stated above, preferably hydrogen, methyl or ethyl, and V is hydroxyl, C.sub.1 -C.sub.4 -alkoxy, allyloxy, trialkylsilyloxy or unsubstituted or substituted benzyloxy, in each case as stated above.

In one aspect, the present invention particularly preferably relates to novel compounds of the general formula IV ##STR5## where X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3 or CHC.sub.2 H.sub.5,

Z is oxygen or NOR.sup.7, R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted and/or fused aryl or unsubstituted or substituted and/or fused hetaryl, in each case as stated above, preferably hydrogen, C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted aryl, particularly preferably hydrogen, methyl or unsubstituted or substituted phenyl, R.sup.7 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, preferably unsubstitued or substituted benzyl, unsubstituted or substituted hetaryl-C.sub.1 -C.sub.4 -alkyl, preferably methyl substituted by five-membered hetaryl, in each case as stated above, or COR.sup.10, R.sup.10 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted aryl or unsubstituted or substituted hetaryl, in each case as stated above, preferably C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted phenyl.

The present invention furthermore particularly preferably relates to novel compounds of the general formula V ##STR6## where X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3 or CHC.sub.2 H.sub.5,

Y is oxygen or NR.sup.4, R.sup.3 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted and/or fused aryl, unsubstituted or substituted and/or fused hetaryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted hetaryl-C.sub.1 -C.sub.4 -alkyl, in each case as stated above, and R.sup.4 is hydrogen or C.sub.1 -C.sub.4 -alkyl, preferably hydrogen, methyl or ethyl.

The novel compounds can be prepared, for example, by the methods shown in the synthesis schemes below. In all schemes, unless restrictions are specifically mentioned, A is an abbreviation for the group R.sup.3 --(Y).sub.n -- defined in claim 1, R is an aliphatic, aromatic or heterocyclic radical and R' may furthermore be hydrogen. B is one of the groups ##STR7## or a fragment from which one of these groups can be synthesized. ##STR8## a N-methylmorpholine N-oxide, .DELTA.T b A--COCH.sub.3, base or acid, if necessary a dehydrating agent

e.g. A--CO--CH.sub.2 --COOtBu, piperidine/p-TsOH, then CF.sub.3 COOH, then .DELTA.T d A--CO--CH.dbd.PR.sub.3 or A--CO--CH.sub.2 P(.dbd.O)Z.sub.2 (Z.dbd.Ar, O-Alkyl)/base e LiCH.sub.2 PO(OR).sub.2, A--CN f A--CO--CH.sub.2 --CO--A, NaOMe g H.sub.2, Pd/C h PdCl.sub.2 (PhCN).sub.2, AgOSO.sub.2 CF.sub.3 or Sn(OSO.sub.2 CF.sub.3).sub.2, N-methylmorpholine .DELTA.T=elevated temperatures, p-TsOH=p-toluenesulfonic acid.

Scheme I shows methods for synthesizing the carbonyl compounds of type 3 or 4 (A.dbd.H, alkyl, aryl, hetaryl, organyloxy, organylthio or mono- or diorganylamino). The .alpha.,.beta.-unsaturated compounds 3 can advantageously be synthesized from aldehydes 2, which can be achieved by aldol [Org. Synth. Coll. I (1941), 77] or Knoevenagel condensation with subsequent elimination of a carbonyl or carboxyl function [Acta Chem. Scand. 17 (1963), 2316], as well as by Wittig [J. Chem. Soc. (1961), 1266] or Horner-Wadsworth-Emmons olefination [Review Org. React. 25 (1977), 73]. Chalcones (i.e. A=aryl) can also be synthesized in a one-vessel reaction by reacting lithiomethanephosphonic esters with aromatic nitriles and the aldehydes 2 [Synthesis (1991), 213].

The aldehydes of type 2 can be prepared by the method described in European Patent 393,428 from the benzyl bromides 1 [for preparation, see European Patents 226,917, 337,211 and 363,818]. The ketones, esters and 1,3-dicarbonyl compounds required for the condensation reactions are generally known building blocks of organic synthesis; the carbonyl-substituted Wittig and Horner reagents are either known or can be synthesized by methods known from the literature [Ang. Chem. 72 (1960), 572 and 73 (1961), 27; Chem. Ber. 95 (1962), 1513; Org. Synth. Coll. VI (1988), 448].

The saturated carbonyl compounds 4 can be prepared from the benzyl bromides 1 by reaction with .beta.-dicarbonyl compounds with elimination of one of the two carbonyl groups (J. Org. Chem. 30 (1965), 3321]; on the other hand, they can be synthesized from the unsaturated analogs 3, for example by hydrogenation [Org. Synth. Coll. I (1941), 101; J. Am. Chem. Soc.111 (1989), 1063]. Conversely, the preparation of carbonyl-substituted alkenes 3 from the analogous alkanes 4 is also possible [Chem. Lett. (1983), 1207].

The methods denoted by a, b, d, f and g in Scheme I are also suitable for the preparation of the substances which are analogous to the compounds 2, 3 and 4 and in which R.sup.1 and R.sup.2 (cf. claim 1, 7 or 8) are not hydrogen. ##STR9## a RNH.sub.2, H.sup.+, dehydration (azeotropic distillation, molecular sieve)

b RR'N--NH.sub.2.HCl or .H.sub.2 SO.sub.4, .DELTA.T c H.sub.2 NOH.HCl, .DELTA.T and/or d H.sub.2 NOR.HCl, .DELTA.T and/or auxiliary base (e.g. pyridine) e R--Br, base (eg. NaOCH.sub.3, K.sub.2 CO.sub.3) f R--COCl, pyridine

Scheme II shows possibilities for converting the aldehdyes and ketones of type 3a (A.dbd.H, organyl) into the N-functional derivatives by standard methods. Thus, imines 5 [Bull. Soc. Chim. Belg. 81 (1972), 643], hydrazones 6 [J. Am. Chem. Soc. 90 (1968), 6821] and oximes [Helv. Chim. Acta 60 (1977), 2294] 7b and oxime ethers 7b [J. Org. Chem. 38 (1973), 3749] are obtainable by condensation of the carbonyl compounds 3a with amines, hydrazines and hydroxylamines or alkoxyamines. For the preparation of the oxime ethers 7b, a two-stage synthesis (conversion of 3a to free oxime 7a, followed by O-alkylation [Helv. Chim. Acta 60 (1977), 2294]) may be advantageous. Oxime esters 7c can likewise be obtained from the oximes 7a by reaction with an acyl chloride/pyridine [J. Org. Chem. 33 (1968), 150].

The reactions described in Scheme II are also suitable for the preparation of analogous compounds in which R.sup.1 and/or R.sup.2 are not H. ##STR10## a CF.sub.3 COOH, .DELTA.T b PdCl.sub.2 or Pd(OOCCH.sub.3).sub.2, PPh.sub.3

c RR'NH, carboxyl-activating agent (eg. di-2-pyridyl disulfide or Ph.sub.2 P(.dbd.O)Cl) d R--Br, base (eg. K.sub.2 CO.sub.3) RSH, carboxyl-activating agent (eg. dicyclohexylcarbodiimide) f chlorinating agent (eg. SOCl.sub.2), .DELTA.T g RR'NH; if necessary+pyridine, N(C.sub.2 H.sub.5).sub.3 h ROH, pyridine N(C.sub.2 H.sub.5).sub.3 i RSH, pyridine, N(C.sub.2 H.sub.5).sub.3

The synthesis of cinnamic acid derivatives of type 3 (A.dbd.OR, SR, NRR') is illustrated in Scheme III. It is advantageously carried out via carboxylic esters 9a (corresponding to type 3 with A.dbd.OR) which can be prepared according to Scheme I and can be hydrolyzed under nonbasic conditions to give the acid 10, for example tert-butyl esters [in acidic medium, J. Am. Chem. Soc. 99 (1977), 2353] or allyl esters [with palladium compounds, Tetrahedron Lett. (1979), 613]. The carboxylic acids 10 can be converted by known methods to, inter alia, mono- or disubstitutedamides 12 [Tetrahedron Lett. (1970), 1901; Synthesis (1980), 385], other esters 9b [European Patent 310,954 and Synthesis (1975), 805] or thioesters 13 [J. Chem. Soc. (C) (1966), 540]. The preparation of such derivatives can also be carried out by the generally known method via the acyl chloride 11 (obtainable by reacting the carboxylic acid 10 with a chlorinating agent, such as thionyl chloride, phosphorus trichloride, phosphoryl chloride or phosgene) by a nucleophilic substitution of the chlorine atom in 11.

The reactions described in Scheme III are also suitable for the preparation of analogous compounds in which R.sup.1 and/or R.sup.2 are not H.

The reaction routes shown in Schemes II and III are also suitable for converting the saturated carbonyl compounds 4 into the corresponding derivatives. Conversion of the (.alpha.,.beta.-unsaturated) products described in the two schemes into their saturated analogs is also possible under suitable hydrogenating or reduction conditions.

Preparation Examples for selected compounds

EXAMPLE 1

Methyl 2-methoximino-2-{2-[3-oxoprop-(E)1-enyl]-phenyl}-acetate (compound No. 77 from Table I)

26.4 g (120 mmol) of methyl 2-methoximino-2-(2-formylphenyl)-acetate (for preparation, see European Patent 393,428, page 3) and 45.6 g of triphenylphosphoranylideneacetaldehyde in 500 ml of toluene are stirred under nitrogen for 20 hours at 60.degree. C. The mixture is cooled and then evaporated down, the residue is taken up in tert-butyl methyl ether/n-hexane, the insoluble substance (triphenylphosphine oxide) is filtered off under suction, the filtrate is evaporated down, diethyl ether is added and the flask is placed in an ice bath. Precipitated Ph.sub.3 PO is likewise filtered off under suction, and the filtrate is evaporated down. Column chromatography (from 95:5 to 90:10 cyclohexane/ethyl acetate) gives 23.8 g (80%) of the title compound as yellowish crystals of melting point 90.degree.-94.degree. C. The product is contaminated with about 10% of the vinylog methyl 2-methoximino-2-{2-[5-oxopenta-(E)1,(E)3-dienyl]-phenyl}-acetate.

.sup.1 H-NMR (CDCl.sub.3, .delta. scale): 3.88 and 4.04 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 6.70 (dd, 1H, CH.dbd.CH--CHO), 7.1-7.7 (m, together 5H, aromatic protons and CH.dbd.CH--CHO); 9.66 (d, 1H, CHO)

EXAMPLE 2

Methyl 2-methoximino-2-{2-[3-(2-chloroprop-2-enyloximino-prop-(E)1-enyl]-phenyl}-acetate (compound No. 57 from Table VI)

3.7 g (15 mmol) of methyl 2-methoximino-2-{2-[3-oxoprop-(E)1-enyl]-phenyl}-acetate (Example 1) and 2.3 g (15mmol) of 2-chloroprop-2-enyloxyamine hydrochloride in 200 ml of tetrahydrofuran (THF) are refluxed for 1 hour. The mixture is allowed to cool, washed twice with saturated sodium chloride solution, dried over magnesium sulfate and evaporated down. Purification by column chromatography (9:1 cyclohexane/ethyl acetate, KG 60) gives the title compound (yellow oil, 2.9 g/58%) as a 4:1 mixture of the anti and syn isomers of the oxime ether.

.sup.1 H-NMR (CDCl.sub.3, .delta. scale), anti-isomer: 3.88 and 4.04 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 4.76 (s, 2H, H.sub.2 C.dbd.CCl--CH.sub.2 O); 5.42 and 5.48 (2 s, each 1H, H.sub.2 C.dbd.CCl); 6.60 and 6.82 (2 d, each 1H, CH.dbd.CH--C.dbd.N), 7.1-7.8 (m, 4H, aromatic protons); 7.92 (d, 1H, CH=N)

EXAMPLE 3

Methyl 2-{2-[3-oxobut-(E)1-enyl]-phenyl}-3-methoxyprop-(E)2 -enoate (compound No. 2 from Table I)

29 g (130 mmol) of methyl (2-formylphenyl)-3-methoxyprop-(E)2-enoate (for preparation, see European Patent 393,428, page 3) and 3.9 g (120 mmol) of triphenylphosphoranylideneacetone in 500 ml of toluene are stirred under nitrogen for 14 hours at 65.degree. C. The mixture is allowed to cool and is evaporated down, the residue is taken up in diethyl ether, the solid (mainly Ph.sub.3 PO) is filtered off under suction and the solvent is stripped off under reduced pressure. Column chromatography gives the title compound (21.4 g/69%) as a brownish oil, sufficiently pure for further reactions. A crystalline product (mp. 69.degree.-71.degree. C.) is obtained by recrystallization from ether/pentane.

.sup.1 H-NMR (CDCl.sub.3, d scale): 2.32 (s, 3H, CH.sub.3 --C.dbd.O); 3.71 and 3.81 (2 s, each 3H, COOCH.sub.3 and CH--OCH.sub.3); 6.70 (d, 1H, CH.dbd.CH--C.dbd.O), 7.2-7.5 (m, together 3H) and 7.72 (d, 1H; aromatic protons); 7.53 (d, 1H, CH.dbd.CH--C.dbd.O); 7.68 (s, 1H, CH--OCH.sub.3)

EXAMPLE 4

Methyl 2-{2-[3-methoximinobut-(E)1-enyl]-phenyl}-3-methoxyprop-(E)2-enoate (compound No. 22 from Table VI)

4.0 g (15 mmol) of methyl 2-{2-[3-oxobut-(E)1-enyl]-phenyl}-3-methoxyprop-(E)2-enoate (Example 3) and 1.3 g (15 mmol) of methoxyamine hydrochloride in 100 ml of methanol are refluxed for 1 hour. The mixture is cooled, after which the methanol is stripped off, the residue is taken up in diethyl ether and the solution is washed with water, dried over magnesium sulfate and evaporated down. The title compound is purified by column chromatography (95:5 cyclohexane/ethyl acetate) and is separated into its C.dbd.N double bond isomers (less polar: anti-oxime ether, oil, 1.4 g; more polar: synoxime ether, oil, 0.5 g; together 1.9 g/44%).

(m, together 3H) and 7.67 (d, 1H; aromatic protons); 7.60 (s, 1H, CH--OCH.sub.3)

EXAMPLE 5

Methyl 2-methoximino-2-{2-[3-oxobut-(E)1-enyl]-phenyl}-acetate (compound No. 78 from Table I)

50 g (226 mmol) of methyl 2-methoximino-2-(2-formylphenyl)-acetate (European Patent 393,428, page 3) and 72 g (227 mmol) of triphenylphosphoranylideneacetone in 1000 ml of toluene are stirred under nitrogen for 5 hours at 65.degree. C. The mixture is allowed to cool, the solvent is stripped off in a rotary evaporator and the title compound (46.9 g/80%) is obtained as yellowish crystals of melting point 115.degree.-117.degree. C. by recrystallization from isopropanol.

.sup.1 H-NMR (CDCl.sub.3, d scale): 2.35 (s, 3H, CH.sub.3 --C.dbd.O); 3.92 and 4.04 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 6.69 (d, 1H, CH.dbd.CH--C.dbd.O); 7.26 (mc, 1H), 7.47 (mc, 2H) and 7.75 (mc, 1H; aromatic protons); 7.31 (d, 1H, CH.dbd.CH--C.dbd.O)

EXAMPLE 6

Methyl 2-methoximino-2-{2-[3-hydroxyiminobut-(E)1-enyl]-phenyl}-acetate (compound No. 71 from Table VI)

10.4 g (40 mmol) of methyl 2-methoximino-2-{2-[3-oxobut-(E)1-enyl]-phenyl}-acetate (Example 5) and 3.1 g (44 mmol) of hydroxylamine hydrochloride in 200 ml of methanol are refluxed for 1 hour. After cooling, the reaction mixture is evaporated down, the residue is digested in diethyl ether and the solid is filtered off under suction. Column chromatography gives the title compound as separate C.dbd.N double bond isomers (less polar: syn-oxime, 2.5 g, colorless crystals, mp. 127.degree.-130.degree. C.; more polar: anti-oxime, 5.0 g, mp. 136.degree.-138.degree. C.; together 7.5 g/68%).

.sup.1 H-NMR (CDCl.sub.3, d scale): syn-isomer, 2.07 (s, 3H, CH.sub.3 --C.dbd.N); 3.98 and 4.06 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 6.72 (d, 1H, CH.dbd.CH--C.dbd.N); 7.00 (mc, 1H), 7.3-7.5 (m, 2H) and 7.80 (mc, 1H; aromatic protons), 7.54 (d, 1H, CH.dbd.CH--C.dbd.N); 8.45 (br, 1H, N--OH)/anti-isomer, 2.08 (s, 3 H, CH.sub.3 --C.dbd.N); 3.90 and 4.05 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 6.73 (d, 1H, CH.dbd.CH--C.dbd.N; 7.20 (mc, 1H), 7.43 (mc, 2H) and 7.79 (mc, 1H; aromatic protons), 7.53 (d, 1H, CH.dbd.CH--C.dbd.N); 8.45 (br, 1H, N--OH)

EXAMPLE 7

Methyl 2-methoximino-2-{2-[3-anti-2,6-difluorobenzyl-oximinobut-(E)1-enyl]-phenyl}-acetate (compound No. 107 from Table VII)

0.9 g (15.2 mmol) of powdered potassium hydroxide is added to 4.0 g (15.2 mmol) of methyl 2-methoximino-2-{2-[3-anti-hydroximinobut-(E)1-enyl]-phenyl}-acetate (Example 6) in 60 ml of dimethylformamide at +5.degree. C. and a solution of 3.1 g (15.2 mmol) of 2,6-difluorobenzyl bromide in 20 ml of dimethylformamide is added dropwise at this temperature. Stirring is carried out for a further hour at +5.degree. C. and the reaction mixture is poured into ice water, extracted 3 times with diethyl ether, dried over magnesium sulfate and evaporated down. Chromatography (9:1 cyclohexane/ethyl acetate, KG 60) gives the title compound (1.2 g/20%) as colorless crystals of melting point 120.degree.-122.degree. C. .sup.1 H-NMR (CDCl.sub.3, d scale): 1.98 (s, 3H, CH.sub.3 --C.dbd.N); 3.87 and 4.01 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3 ; 5.24 (s, 2H, Ar--CH.sub.2 --O); 6.60 and 6.80 (2 d, each 1H, CH--CH.dbd.C.dbd.N); 6.93 (mc, 2H), 7.1-7.5 (m, 6H) and 7.70 (mc, 1H; aromatic protons)

EXAMPLE 8

Methyl 2-methoximino-2-{2-[3-benzyloximinobut-(E)1-enyl]-phenyl}-acetate (compound No. 83 from Table VI)

2.0 g (7.6 mmol) of methyl 2-methoximino-2-{2-[3-oxobut-(E)1-enyl]-phenyl}-acetate (Example 5) and 1.2 g (7.6 mmol) of benzyloxyamine are dissolved in 60 ml of methanol, 1 ml of concentrated hydrochloric acid is added and the reaction mixture is refluxed for 1 hour. It is allowed to cool and is evaporated down, the residue is taken up in diethyl ether, the solution is washed with water and dried over magnesium sulfate and the solvent is stripped off. Column chromatography (from 95:5 to 90:10 cyclohexane/ethyl acetate) gives the title compound as separate C.dbd.N double bond isomers (less polar: anti-oxime ether, 1.1 g, oil; more polar: syn-oxime ether, 0.6 g, oil; together 1.7 g/61%).

.sup.1 H-NMR (CDCl.sub.3, d scale): anti-isomer: 2.04 (s, 3H, CH.sub.3 --C.dbd.N); 3.88 and 4.03 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 5.24 (s, 2H, Ar--CH.sub.2 --O); 6.62 and 6.82 (2 d, each 1H, CH.dbd.CH--C.dbd.N); 7.17 (mc, 1H), 7.3-7.5 (m, 7H) and 7.69 (mc, 1H; aromatic protons)

EXAMPLE 9

Methyl 2-methoximino-2-{2-[3-anti-phenylhydrazonobut-(E)1-enyl]-phenyl}-acetate (compound No. 68 from Table VII)

2.6 g (10 mmol) of methyl 2-methoximino-2-{2-[3-oxobut-(E)1-enyl]-phenyl}-acetate (Example 5) and 1.08 g (10 mmol) of phenylhydrazine in 50 ml of methanol are refluxed for 4 hours. The mixture is allowed to cool, the solvent is stripped off and the product is purified by column chromatography (80:20 cyclohexane/ethyl acetate, KG 60). The anti-hydrazone (oil, 1.5 g/43%) is obtained as the only defined product in the form of yellow crystals from diethyl ether (mp. 155.degree.-158.degree. C.).

.sup.1 H-NMR (CDCl.sub.3, d scale): 1.99 (s, 3H, CH.sub.3 --C.dbd.N); 3.86 and 4.05 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 6.48 (d, 1H, CH.dbd.CH--C.dbd.N); 6.86 (t, 1H), 7.1-7.5 (m, 7H) and 7.74 (d, 1H; aromatic protons); 7.02 (d, 1H, CH.dbd.CH--C.dbd.N)

EXAMPLE 10

Methyl 2-methoximino-2-{2-[3-oxo-3-(4-methoxyphenyl)prop-(E)1-enyl]-phenyl}-acetate (compound No. 57 from Table II)

7.7 g (35 mmol) of Methyl 2-methoximino-2-(2-formylphenyl)-acetate (European Patent 393,428, page 3) and 15.5 g (38 mmol) of triphenylphosphoranylidene-4-methoxyacetophenone in 300 ml of toluene are refluxed for 2 hours. The mixture is cooled and then evaporated down and the residue is subjected to column chromatography (from 95:5 to 85:15 cyclohexane/ethyl acetate, KG 60). The title compound (9.7 g/69%) is obtained as virtually colorless crystals (mp. 137.degree.-141.degree. C.).

.sup.1 H-NMR (CDCl, d scale): 3.86, 3.91 and 4.10 (3 s, each 3H, COOCH.sub.3, NOCH.sub.3 and Ar--OCH.sub.3); 7.00 and 8.02 (2 d, each 2H, protons in p-disubstituted aromatics); 7.2-7.9 (m, 6H, protons in o-disubstituted aromatics and CH.dbd.CH--C.dbd.O)

EXAMPLE 11

Methyl 2-methoximino-2-{2-[3-methoximino-3-(4-methoxyphenyl)-prop-(E)1-enyl]-phenyl}-acetate (compound No. 97 from Table VI)

3.5 g (10 mmol) of methyl 2-methoximino-2-{2-[3-oxo-3-(4-methoxyphenyl)-prop-(E)1-enyl]-phenyl}-acetate (Example 10) and 1.0 g (12 mmol) of methoxyamine hydrochloride are refluxed for 2 hours. The mixture is allowed to reach room temperature (20.degree. C., RT) and the methanol is stripped off. Column chromatography (9:1 cyclohexane/ethyl acetate, KG 60) is the title compound (anti/syn isomer mixture, 0.9 g/24%) as a brownish oil which can be crystallized from pentane/diethyl ether (mp. 100.degree.-104.degree. C.).

.sup.1 H-NMR (CDCl.sub.3, d scale): 3.80, 3.82, 3.94 and 4.01 (4 s, each 3H, COOCH.sub.3, both NOCH.sub.3 and Ar--OCH.sub.3 in anti-isomer); 3.78, 3.83, 3.90 and 3.92 (4 s, each 3H, COOCH.sub.3, both NOCH.sub.3 and Ar--OCH.sub.3 in syn-isomer); 6.30 (d, 1H, CH.dbd.CH--C.dbd.N in syn-isomer); 6.60 (d, 1H, CH.dbd.CH--C.dbd.N in anti-isomer); 6.85-7.9 (m, 9H, aromatic protons and CH.dbd.CH--C.dbd.N in both isomers)

EXAMPLE 12

Methyl 2-methoximino-2-{2-[2-tert-butoxycarbonyl-(E)-ethenyl]-phenyl}-acetate (compound No. 112 from Table I)

17.6 g (80 mmol) of methyl 2-methoximino-2-(2-formylphenyl)-acetate (European Patent 393,428, page 3) and 33 g (88 mmol) of tert-butyl triphenylphosphoranylideneacetate in 500 ml of toluene are stirred under nitrogen for 1 hour at 60.degree. C. The mixture is allowed to cool, the solvent is stripped off, diethyl ether is added to the residue and the mixture is placed in an ice bath. The major amount of triphenylphosphine oxide separates out and is filtered off under suction. The filtrate is evaporated down and the residue is purified by column chromatography (from 95:5 to 93:7 cyclohexane/ethyl acetate). The title compound (24 g/94%) is obtained as a brownish oil.

.sup.1 H-NMR (CDCl.sub.3, d scale): 1.53 (s, 9H, (CH.sub.3).sub.3 CO); 3.85 and 4.03 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 6.33 (d, 1H, CH.dbd.CH--C.dbd.O); 7.1-7.75 (m, 5H, aromatic protons and CH.dbd.CH--C.dbd.O)

EXAMPLE 13

Methyl 2-methoximino-2-{2-[2-carboxyl-(E)ethenyl]-phenyl}-acetate (compound No. 109 from Table I)

A solution of 18 g (48 mmol) of methyl 2-methoximino-2-{2-[2-tert-butoxycarbonyl-(E)ethenyl]phenyl}-acetate (Example 12) in 100 ml of THF is stirred with 20 ml of concentrated hydrochloric acid for 45 minutes at 65.degree. C. The mixture is allowed to cool, the solvent is stripped off, the remaining crystal slurry is triturated with diisopropyl ether/pentane and the solid is filtered off under suction and dried. The title compound (12 g/81%) is obtained as beige crystals (mp. 178.degree.-182.degree. C.).

.sup.1 H-NMR (CDCl.sub.3, d scale): 3.93 and 4.09 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 6.48, d, 1H, CH.dbd.CH--C.dbd.O); 7.23 (mc, 1H), 7.50 (mc, 2H) and 7.78 (mc, 1H; aromatic protons); 7.59 (d, 1H, CH.dbd.CH--C.dbd.O); 10.8 (broad, 1H, COOH)

EXAMPLE 14

Methyl 2-methoximino-2-{2-[2-(2,6-difluorobenzyloxy-carbonyl-(E)ethenyl]-phenyl}-acetate (compound No. 37 from Table III)

3.4 g (13 mmol) of methyl 2-methoximino-2-{2-[2-carboxyl-(E)ethenyl]-phenyl}-acetate (Example 13) are dissolved in 50 ml of dimethylformamide, the solution is cooled to +5.degree. C. and 0.75 g (13 mmol) of powdered potassium hydroxide is added. A solution of 2.7 g (13 mmol) of 2,6-difluorobenzyl bromide in 15 ml of dimethylformamide is added dropwise at the same temperature, after which the reaction mixture is allowed to reach room temperature and is stirred for a further hour. The reaction mixture is stirred into ice water and extracted 3 times with diethyl ether and the combined extracts are washed with water, dried and evaporated down. Trituration of the oily residue with diisopropyl ether gives the title compound (3.2 g/63%) in crystalline form (mp. 108.degree.-110.degree. C.).

.sup.1 H-NMR (CDCl.sub.3, d scale): 3.91 and 4.06 (2 s, each 3H, COOCH.sub.3 and NOCH.sub.3); 5.31 (s, 2H, Ar--CH.sub.2 --O); 6.42 (d, 1H, CH.dbd.CH--C.dbd.O); 6.95 (mc, 2H) and 7.1-7.8 (m, 6H; aromatic protons and CH.dbd.CH--C.dbd.O)

EXAMPLE 15

Methyl 2-methoximino-2-{2-[3-oxo-3-phenyl)propyl]-phenyl}-acetate (compound No. 50 from Table X)

5.0 g (17.5 mmol) of methyl 2-methoximino-2-(2-bromomethylphenyl)-acetate (European Patent 363,818, page 3) and 3.9 g (17.5 mmol) of dibenzoylmethane are dissolved in 50 ml of methanol, and 2.7 g (19.3 mmol) of potassium carbonate and a pinch of potassium iodide are added. Stirring is carried out for 90 minutes under reflux, the mixture is allowed to cool and the solvent is stripped off. Water is added to the residue, the latter is extracted twice with methylene chloride and the combined extracts are dried over magnesium sulfate and evaporated down. Flash chromatography (from 90:10 to 75:25 n-hexane/ethyl acetate) gives the title compound (1.4 g/25%) as a deep red oil.

IR (KBr, .about., in cm.sup.-1): 1722, 1689, 1218, 1205, 1067, 1049, 1015, 957, 748, 689

Examples of compounds preferred because of their action as pesticides are shown in the Tables below.

The double bond C.dbd.X in the Tables below has an E (or anti) configuration, unless stated otherwise, and has a double bond between the carbon atoms substituted by R.sup.1 and R.sup.2 in the general formula I. If only one stereoisomer was isolated in the compounds having a C.dbd.N double bond in the side chain (ie. Z.dbd.N--R.sup.6, N--OR.sup.7 or N--NR.sup.8 R.sup.9), or if the isomers were separated, the configuration is specified in a column headed Isomer by the letters a (for anti) and s (for syn). Mixtures of the two forms which have not been separated appear in this column as percentages: a(70) and s(30) means a mixture of 70% of anti-isomer and 30% of syn-isomer.

The chemical shift (solvent CDCl.sub.3, standard TMS, .delta. scale) of protons corresponding to R.sup.1 and R.sup.2 was used for characterizing compounds obtained in noncrystalline form.

TABLE I__________________________________________________________________________ ##STR11## m.p.No. A R.sup.1 R.sup.2 X (.degree.C.) .delta. (CC .sub.-- H)__________________________________________________________________________ 1 H H H CHOCH.sub.3 2 CH.sub.3 H H CHOCH.sub.3 69-71 3 C.sub.2 H.sub.5 H H CHOCH.sub.3 4 i-C.sub.3 H.sub.7 H H CHOCH.sub.3 5 n-C.sub.4 H.sub.9 H H CHOCH.sub.3 6 t-C.sub.4 H.sub.9 H H CHOCH.sub.3 oil 7.07/7.67 7 H.sub.2 CCH H H CHOCH.sub.3 8 CH.sub.3 CC H H CHOCH.sub.3 9 Cyclopropyl H H CHOCH.sub.3 10 Cyclohexyl H H CHOCH.sub.3 11 N-Methylpiperidin-2-yl H H CHOCH.sub.3 12 C.sub.6 H.sub. 5 H H CHOCH.sub.3 oil 13 .alpha.-Naphthyl H H CHOCH.sub.3 14 .beta.-Naphthyl H H CHOCH.sub.3 15 2-Pyridyl H H CHOCH.sub.3 16 3-Pyridyl H H CHOCH.sub.3 17 4-Pyridyl H H CHOCH.sub.3 18 6-Chloro-2-pyridyl H H CHOCH.sub.3 19 2-Pyrazinyl H H CHOCH.sub.3 20 2-Quinolinyl H H CHOCH.sub.3 21 2-Furyl H H CHOCH.sub.3 22 3-Thienyl H H CHOCH.sub.3 23 N-Methyl-3-Pyrryl H H CHOCH.sub.3 24 N-Methyl-2-Indolyl H H CHOCH.sub.3 25 C.sub.6 H.sub.5 CH.sub.2 H H CHOCH.sub.3 26 .beta.-Naphthylmethyl H H CHOCH.sub.3 27 2-Pyridylmethyl H H CHOCH.sub.3 28 2-Furylmethyl H H CHOCH.sub.3 29 3-Indolylmethyl H H CHOCH.sub.3 30 C.sub.6 H.sub.5 CHCH H H CHOCH.sub.3 31 2-(2-Furyl)ethenyl H H CHOCH.sub.3 32 CF.sub.2 H H CHOCH.sub.3 33 HO H H CHOCH.sub.3 140-143 34 CH.sub.3 O H H CHOCH.sub.3 35 C.sub.2 H.sub.5 O H H CHOCH.sub.3 36 t-C.sub.4 H.sub.9 O H H CHOCH.sub.3 oil 6.30/7.58 37 H.sub.2 CCHCH.sub.2 O H H CHOCH.sub.3 oil 6.44/7.72 38 C.sub.6 H.sub.5 O H H CHOCH.sub.3 103-104 39 C.sub.6 H.sub.5 CH.sub.2 O H H CHOCH.sub.3 111-112 40 (CH.sub.3).sub.3 SiO H H CHOCH.sub.3 41 t-C.sub.4 H.sub.9(CH.sub.3).sub.2 SiO H H CHOCH.sub.3 42 H.sub.2 N H H CHOCH.sub.3 43 CH.sub.3 NH H H CHOCH.sub.3 44 (CH.sub.3).sub.2 N H H CHOCH.sub.3 45 C.sub.6 H.sub.5 NH H H CHOCH.sub.3 155 (oil) 46 C.sub.6 H.sub.5 NCH.sub.3 H H CHOCH.sub.3 47 C.sub.6 H.sub.5 CH.sub.2 NH H H CHOCH.sub.3 48 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NH H H CHOCH.sub.3 49 2-ClC.sub.6 H.sub.4 CH.sub.2 NH H H CHOCH.sub.3 50 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NH H H CHOCH.sub.3 51 4-Cyano-C.sub.6 H.sub.4CH.sub.2 NH H H CHOCH.sub.3 52 2,6-F.sub.2C.sub.6 H.sub.3CH.sub.2 NH H H CHOCH.sub.3 53 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 H H CHOCH.sub.3 122-124 54 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHOCH.sub.3 55 2-ClC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHOCH.sub.3 56 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHOCH.sub.3 57 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHOCH.sub.3 58 N-Morpholinyl H H CHOCH.sub.3 149-152 59 HS H H CHOCH.sub.3 60 C.sub.6 H.sub.5 CH.sub.2 S H H CHOCH.sub.3 61 CH.sub.3 CH.sub.3 H CHOCH.sub.3 62 C.sub.6 H.sub.5 CH.sub.3 H CHOCH.sub.3 63 t-C.sub.4 H.sub.9 O CH.sub.3 H CHOCH.sub.3 64 C.sub.6 H.sub.5 CH.sub.2 O CH.sub.3 H CHOCH.sub.3 65 CH.sub.3 NH CH.sub.3 H CHOCH.sub.3 66 C.sub.6 H.sub.5 NCH.sub.3 CH.sub.3 H CHOCH.sub.3 67 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CH.sub.3 H CHOCH.sub.3 68 C.sub.6 H.sub.5 CH.sub.2 S CH.sub.3 H CHOCH.sub.3 69 CH.sub.3 H CH.sub.3 CHOCH.sub.3 77-79 70 C.sub.6 H.sub.5 H CH.sub.3 CHOCH.sub.3 71 t-C.sub.4 H.sub.9 O H CH.sub.3 CHOCH.sub.3 oil 7.46 72 C.sub.6 H.sub.5 CH.sub.2 O H CH.sub.3 CHOCH.sub.3 73 CH.sub.3 NH H CH.sub.3 CHOCH.sub.3 74 C.sub.6 H.sub.5 NCH.sub.3 H CH.sub.3 CHOCH.sub.3 75 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 H CH.sub.3 CHOCH.sub.3 76 C.sub.6 H.sub.5 CH.sub.2 S H CH.sub.3 CHOCH.sub.3 77 H H H NOCH.sub.3 90-94 78 CH.sub.3 H H NOCH.sub.3 115-117 79 C.sub.2 H.sub.5 H H NOCH.sub.3 80 i-C.sub.3 H.sub.7 H H NOCH.sub.3 81 n-C.sub.4 H.sub.9 H H NOCH.sub.3 82 t-C.sub.4 H.sub.9 H H NOCH.sub.3 67-69 83 H.sub.2 CCH H H NOCH.sub.3 84 CH.sub.3 C C H H NOCH.sub.3 85 Cyclopropyl H H NOCH.sub.3 86 Cyclohexyl H H NOCH.sub.3 87 N-Methylpiperidin-2-yl H H NOCH.sub.3 88 C.sub.6 H.sub.5 H H NOCH.sub.3 98-102 89 .alpha.-Naphthyl H H NOCH.sub.3 90 .beta.-Naphthyl H H NOCH.sub.3 91 2-Pyridyl H H NOCH.sub.3 92 3-Pyridyl H H NOCH.sub.3 93 4-Pyridyl H H NOCH.sub.3 94 6-Chloro-2-pyridyl H H NOCH.sub.3 95 2-Pyrazinyl H H NOCH.sub.3 96 2-Quinolinyl H H NOCH.sub.3 97 2-Furyl H H NOCH.sub.3 98 3-Thienyl H H NOCH.sub.3 99 N-Methyl-3-Pyrryl H H NOCH.sub.3100 N-Methyl-2-Indolyl H H NOCH.sub.3101 C.sub.6 H.sub.5 CH.sub.2 H H NOCH.sub.3102 .beta.-Naphthylmethyl H H NOCH.sub.3103 2-Pyridylmethyl H H NOCH.sub.3104 2-Furylmethyl H H NOCH.sub.3105 3-Indolylmethyl H H NOCH.sub.3106 C.sub.6 H.sub.5 CHCH H H NOCH.sub.3107 2-(2-Furyl)ethenyl H H NOCH.sub.3108 CF.sub.3 H H NOCH.sub.3109 HO H H NOCH.sub.3 178-182110 CH.sub.3 O H H NOCH.sub.3 oil 6.40/7.10111 C.sub.2 H.sub.5 O H H NOCH.sub.3112 t-C.sub.4 H.sub.9 O H H NOCH.sub.3 oil 6.33/7.39113 H.sub.2 CCHCH.sub.2 O H H NOCH.sub.3 oil 6.45/7.52114 C.sub.6 H.sub.5 O H H NOCH.sub.3 110115 C.sub.6 H.sub.5 CH.sub.2 O H H NOCH.sub.3 oil 6.49/7.54116 (CH.sub.3).sub.3 SiO H H NOCH.sub.3117 t-C.sub.4 H.sub.9(CH.sub.3).sub.2 SiO H H NOCH.sub.3118 H.sub.2 N H H NOCH.sub.3119 CH.sub.3 NH H H NOCH.sub.3120 (CH.sub.3).sub.2 N H H NOCH.sub.3121 C.sub.6 H.sub.5 NH H H NOCH.sub.3 115-117112 C.sub.6 H.sub.5 NCH.sub.3 H H NOCH.sub.3 136-138123 C.sub.6 H.sub.5 CH.sub.2 NH H H NOCH.sub.3 107-110124 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NH H H NOCH.sub.3125 2-ClC.sub.6 H.sub.4 CH.sub.2 NH H H NOCH.sub.3126 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NH H H NOCH.sub.3127 4-Cyano-C.sub.6 H.sub.4CH.sub.2 NH H H NOCH.sub.3128 2,6-F.sub.2C.sub.6 H.sub.3CH.sub.2 NH H H NOCH.sub.3129 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 H H NOCH.sub.3 98-101130 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H NOCH.sub.3131 2-ClC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H NOCH.sub.3132 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H NOCH.sub.3133 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H NOCH.sub.3134 N-Morpholinyl H H NOCH.sub.3 132-134135 HS H H NOCH.sub.3136 C.sub.6 H.sub.5 CH.sub.2 S H H NOCH.sub.3137 CH.sub.3 CH.sub.3 H NOCH.sub.3138 C.sub.6 H.sub.5 CH.sub.3 H NOCH.sub.3139 t-C.sub.4 H.sub.9 O CH.sub.3 H NOCH.sub.3140 C.sub.6 H.sub.5 CH.sub.2 O CH.sub.3 H NOCH.sub.3141 CH.sub.3 NH CH.sub.3 H NOCH.sub.3142 C.sub.6 H.sub.5 NCH.sub.3 CH.sub.3 H NOCH.sub.3143 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CH.sub.3 H NOCH.sub.3144 C.sub.6 H.sub.5 CH.sub.2 S CH.sub. 3 H NOCH.sub.3145 CH.sub.3 H CH.sub.3 NOCH.sub.3 oil 7.33146 C.sub.6 H.sub.5 H CH.sub.3 NOCH.sub.3147 t-C.sub.4 H.sub.9 O H CH.sub.3 NOCH.sub.3 oil 7.28148 C.sub.6 H.sub.5 CH.sub.2 O H CH.sub.3 NOCH.sub.3149 CH.sub.3 NH H CH.sub.3 NOCH.sub.3150 C.sub.6 H.sub.5 NCH.sub.3 H CH.sub.3 NOCH.sub.3151 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 H CH.sub.3 NOCH.sub.3152 C.sub.6 H.sub.5 CH.sub.2 S H CH.sub.3 NOCH.sub.3153 H H H CHCH.sub.3154 CH.sub.3 H H CHCH.sub.3155 C.sub.2 H.sub.5 H H CHCH.sub.3156 i-C.sub.3 H.sub.7 H H CHCH.sub.3157 n-C.sub.4 H.sub.9 H H CHCH.sub.3158 t-C.sub.4 H.sub.9 H H CHCH.sub.3159 H.sub.2 CCH H H CHCH.sub.3160 CH.sub.3 CC H H CHCH.sub.3161 Cyclopropyl H H CHCH.sub.3162 Cyclohexyl H H CHCH.sub.3163 N-Methylpiperidin-2-yl H H CHCH.sub.3164 C.sub.6 H.sub.5 H H CHCH.sub.3165 .alpha.-Naphthyl H H CHCH.sub.3166 .beta.-Naphthyl H H CHCH.sub.3167 2-Pyridyl H H CHCH.sub.3168 3-Pyridyl H H CHCH.sub.3169 4-Pyridyl H H CHCH.sub.3170 6-Chloro-2-pyridyl H H CHCH.sub.3171 2-Pyrazinyl H H CHCH.sub.3172 2-Quinolinyl H H CHCH.sub.3173 2-Furyl H H CHCH.sub.3174 3-Thienyl H H CHCH.sub.3175 N-Methyl-3-pyrryl H H CHCH.sub.3176 N-Methyl-2-indolyl H H CHCH.sub.3177 C.sub.6 H.sub.5 CH.sub.2 H H CHCH.sub.3178 .beta.-Naphthylmethyl H H CHCH.sub.3179 2-Pyridylmethyl H H CHCH.sub.3180 2-Furylmethyl H H CHCH.sub.3181 3-Indolylmethyl H H CHCH.sub.3182 C.sub.6 H.sub.5 CHCH H H CHCH.sub.3183 2-(2-Furyl)ethenyl H H CHCH.sub.3184 CF.sub.3 H H CHCH.sub.3185 HO H H CHCH.sub.3186 CH.sub.3 O H H CHCH.sub.3187 C.sub.2 H.sub.5 O H H CHCH.sub.3188 t-C.sub.4 H.sub.9 O H H CHCH.sub.3189 H.sub.2 CCHCH.sub.2 O H H CHCH.sub.3190 C.sub.6 H.sub.5 O H H CHCH.sub.3191 C.sub.6 H.sub.5 CH.sub.2 O H H CHCH.sub. 3192 (CH.sub.3).sub.3 SiO H H CHCH.sub.3193 t-C.sub.4 H.sub.9(CH.sub.3).sub.2 SiO H H CHCH.sub.3194 H.sub.2 N H H CHCH.sub.3195 CH.sub.3 NH H H CHCH.sub.3196 (CH.sub.3).sub.2 N H H CHCH.sub.3197 C.sub.6 H.sub.5 NH H H CHCH.sub.3198 C.sub.6 H.sub.5 NCH.sub.3 H H CHCH.sub.3199 C.sub.6 H.sub.5 CH.sub.2 NH H H CHCH.sub.3200 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NH H H CHCH.sub.3201 2-ClC.sub.6 H.sub.4 CH.sub.2 NH H H CHCH.sub.3202 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NH H H CHCH.sub.3203 4-Cyano-C.sub.6 H.sub.4CH.sub.2 NH H H CHCH.sub.3204 2,6-F.sub.2C.sub.6 H.sub.3CH.sub.2 NH H H CHCH.sub.3205 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 H H CHCH.sub.3206 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHCH.sub.3207 2-ClC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHCH.sub.3208 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHCH.sub.3209 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHCH.sub.3210 N-Morpholinyl H H CHCH.sub.3211 HS H H CHCH.sub.3212 C.sub.6 H.sub.5 CH.sub.2 S H H CHCH.sub.3213 CH.sub.3 CH.sub.3 H CHCH.sub.3214 C.sub.6 H.sub.5 CH.sub.3 H CHCH.sub.3215 t-C.sub.4 H.sub.9 O CH.sub.3 H CHCH.sub.3216 C.sub.6 H.sub.5 CH.sub.2 O CH.sub.3 H CHCH.sub.3217 CH.sub.3 NH CH.sub.3 H CHCH.sub.3218 C.sub.6 H.sub.5 NCH.sub.3 CH.sub.3 H CHCH.sub.3219 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CH.sub.3 H CHCH.sub.3220 C.sub.6 H.sub.5 CH.sub.2 S CH.sub.3 H CHCH.sub.3221 CH.sub.3 H CH.sub.3 CHCH.sub.3222 C.sub.6 H.sub.5 H CH.sub.3 CHCH.sub.3223 t-C.sub.4 H.sub.9 O H CH.sub.3 CHCH.sub.3224 C.sub.6 H.sub.5 CH.sub.2 O H CH.sub.3 CHCH.sub.3225 CH.sub.3 NH H CH.sub.3 CHCH.sub.3226 C.sub.6 H.sub.5 NCH.sub.3 H CH.sub.3 CHCH.sub.3227 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 H CH.sub.3 CHCH.sub.3228 C.sub.6 H.sub.5 CH.sub.2 S H CH.sub.3 CHCH.sub.3229 H H H CHC.sub.2 H.sub.5230 CH.sub.3 H H CHC.sub.2 H.sub.5231 C.sub.2 H.sub.5 H H CHC.sub.2 H.sub.5232 i-C.sub.3 H.sub.7 H H CHC.sub.2 H.sub.5233 n-C.sub.4 H.sub.9 H H CHC.sub.2 H.sub.5234 t-C.sub.4 H.sub.9 H H CHC.sub.2 H.sub.5235 H.sub.2 CCH H H CHC.sub.2 H.sub.5236 CH.sub.3 CC H H CHC.sub.2 H.sub.5237 Cyclopropyl H H CHC.sub.2 H.sub.5238 Cyclohexyl H H CHC.sub.2 H.sub.5239 N-Methylpiperidin-2-yl H H CHC.sub.2 H.sub.5240 C.sub.6 H.sub.5 H H CHC.sub.2 H.sub.5241 .alpha.-Naphthyl H H CHC.sub.2 H.sub.5242 .beta.-Naphthyl H H CHC.sub.2 H.sub.5243 2-Pyridyl H H CHC.sub.2 H.sub.5244 3-Pyridyl H H CHC.sub.2 H.sub.5245 4-Pyridyl H H CHC.sub.2 H.sub.5246 6-Chloro-2-pyridyl H H CHC.sub.2 H.sub.5247 2-Pyrazinyl H H CHC.sub.2 H.sub.5248 2-Quinolinyl H H CHC.sub.2 H.sub.5249 2-Furyl H H CHC.sub.2 H.sub.5250 3-Thienyl H H CHC.sub.2 H.sub.5251 N-Methyl-3-pyrryl H H CHC.sub.2 H.sub.5252 N-Methyl-2-indolyl H H CHC.sub.2 H.sub.5253 C.sub.6 H.sub.5 CH.sub.2 H H CHC.sub.2 H.sub.5254 .beta.-Naphthylmethyl H H CHC.sub.2 H.sub.5255 2-Pyridylmethyl H H CHC.sub.2 H.sub.5256 2-Furylmethyl H H CHC.sub.2 H.sub.5257 3-Indolylmethyl H H CHC.sub.2 H.sub.5258 C.sub.6 H.sub.5 CHCH H H CHC.sub.2 H.sub.5259 2-(2-Furyl)ethenyl H H CHC.sub.2 H.sub.5260 CF.sub.3 H H CHC.sub.2 H.sub.5261 HO H H CHC.sub.2 H.sub.5262 CH.sub.3 O H H CHC.sub.2 H.sub.5263 C.sub.2 H.sub.5 O H H CHC.sub.2 H.sub.5264 t-C.sub.4 H.sub.9 O H H CHC.sub.2 H.sub.5265 H.sub.2 CCHCH.sub.2 O H H CHC.sub.2 H.sub.5266 C.sub.6 H.sub.5 O H H CHC.sub.2 H.sub.5267 C.sub.6 H.sub.5 CH.sub.2 O H H CHC.sub. 2 H.sub.5268 (CH.sub.3).sub.3 SiO H H CHC.sub.2 H.sub.5269 t-C.sub.4 H.sub.9(CH.sub.3).sub.2 SiO H H CHC.sub.2 H.sub.5270 H.sub.2 N H H CHC.sub.2 H.sub.5271 CH.sub.3 NH H H CHC.sub.2 H.sub.5272 (CH.sub.3).sub.2 N H H CHC.sub.2 H.sub.5273 C.sub.6 H.sub.5 NH H H CHC.sub.2 H.sub.5274 C.sub.6 H.sub.5 NCH.sub.3 H H CHC.sub.2 H.sub.5275 C.sub.6 H.sub.5 CH.sub.2 NH H H CHC.sub.2 H.sub.5276 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NH H H CHC.sub.2 H.sub.5277 2-ClC.sub.6 H.sub.4 CH.sub.2 NH H H CHC.sub.2 H.sub.5278 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NH H H CHC.sub.2 H.sub.5279 4-Cyano-C.sub.6 H.sub.4CH.sub.2 NH H H CHC.sub.2 H.sub.5280 2,6-F.sub.2C.sub.6 H.sub.3CH.sub.2 NH H H CHC.sub.2 H.sub.5281 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 H H CHC.sub.2 H.sub.5282 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHC.sub.2 H.sub.5283 2-ClC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHC.sub.3 H.sub.5284 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHC.sub.2 H.sub.5285 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 H H CHC.sub.2 H.sub.5286 N-Morpholinyl H H CHC.sub.2 H.sub.5287 HS H H CHC.sub.2 H.sub.5288 C.sub.6 H.sub.5 CH.sub.2 S H H CHC.sub.2 H.sub.5289 CH.sub.3 CH.sub.3 H CHC.sub.2 H.sub.5290 C.sub.6 H.sub.5 CH.sub.3 H CHC.sub.2 H.sub.5291 t-C.sub.4 H.sub.9 O CH.sub.3 H CHC.sub.2 H.sub.5292 C.sub.6 H.sub.5 CH.sub.2 O CH.sub.3 H CHC.sub.2 H.sub.5293 CH.sub.3 NH CH.sub.3 H CHC.sub.2 H.sub.5294 C.sub.6 H.sub.5 NCH.sub.3 CH.sub.3 H CHC.sub.2 H.sub.5295 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CH.sub.3 H CHC.sub.2 H.sub.5296 C.sub.6 H.sub.5 CH.sub.2 S CH.sub.3 H CHC.sub.2 H.sub.5297 CH.sub.3 H CH.sub.3 CHC.sub.2 H.sub.5298 C.sub.6 H.sub.5 H CH.sub.3 CHC.sub.2 H.sub.5299 t-C.sub.4 H.sub.9 O H CH.sub.3 CHC.sub.2 H.sub.5300 C.sub.6 H.sub.5 CH.sub.2 O H CH.sub.3 CHC.sub.2 H.sub.5301 CH.sub.3 NH H CH.sub.3 CHC.sub.2 H.sub.5302 C.sub.6 H.sub.5 NCH.sub.3 H CH.sub.3 CHC.sub.2 H.sub.5303 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 H CH.sub.3 CHC.sub.2 H.sub.5304 C.sub.6 H.sub.5 CH.sub.2 S H CH.sub.3 CHC.sub.2 H.sub.5305 2-CH.sub.3C.sub.6 H.sub.4 O H H CHOCH.sub.3 oil 6.61/7.89306 3-CH.sub.3C.sub.6 H.sub.4 O H H CHOCH.sub.3 oil 6.60/7.87307 4-CH.sub.3C.sub.6 H.sub.4 O H H CHOCH.sub.3308 3-CF.sub.3C.sub.6 H.sub.4 O H H CHOCH.sub.3 oil 6.60/7.88309 4-ClC.sub.6 H.sub.4 O H H CHOCH.sub.3310 4-t-C.sub.4 H.sub.9C.sub.6 H.sub.4 O H H CHOCH.sub.3 106-107311 4-CH.sub.3 ONC(CH.sub.3)C.sub.6 H.sub.4 O H H CHOCH.sub.3 136-138312 3,4-Cl.sub.2 C.sub.6 H.sub.3 O H H CHOCH.sub.3 88-90313 3,5-Cl.sub.2C.sub.6 H.sub.3 O H H CHOCH.sub.3 93-95314 2-Phenyloxazol-4-yl- H H CHOCH.sub.3 oil 6.48/7.33 methoxy315 CH.sub.3 OOCCH.sub.2 O H H CHOCH.sub.3 oil 6.47/7.78316 t-C.sub.4 H.sub.9 OOCCH.sub.2 O H H CHOCH.sub.3 oil 6.47/7.76317 t-C.sub.4 H.sub.9 NH H H CHOCH.sub.3 168-169318 CH.sub.3 OOOCH(CH.sub.3)NH H H CHOCH.sub.3 130-133319 CH.sub.3 OOCCH(i-C.sub.4 H.sub.9)NH H H CHOCH.sub.3 142-144320 Piperidin-1-yl H H CHOCH.sub.3 134-135321 CH.sub.2C(CH.sub.3)CH.sub.2 ONH H H CHOCH.sub.3322 CH.sub.2CClCH.sub.2 ONH H H CHOCH.sub.3323 3',4'-Cl.sub.2C.sub.6 H.sub.3CH.sub.2 ONH H H CHOCH.sub.3 112-114324 HO H CH.sub.3 CHOCH.sub.3 7.73325 2-CH.sub.3C.sub.6 H.sub.4 O H CH.sub.3 CHOCH.sub.3326 3-CF.sub.3C.sub.6 H.sub.4 O H CH.sub.3 CHOCH.sub.3327 4-ClC.sub. 6 H.sub.4 O H CH.sub.3 CHOCH.sub.3328 3,5-Cl.sub.2C.sub.6 H.sub.4 O H CH.sub.3 CHOCH.sub.3329 2-CH.sub.3C.sub.6 H.sub.4 O H H NOCH.sub.3 oil 6.63/7.69330 3-CH.sub.3C.sub.6 H.sub.4 O H H NOCH.sub.3 86-87331 4-CH.sub.3 C.sub.6 H.sub.4 O H H NOCH.sub.3332 3-CF.sub.3C.sub.6 H.sub.4 O H H NOCH.sub.3 96-98333 4-ClC.sub.6 H.sub.4 O H H NOCH.sub.3334 4-t-C.sub.4 H.sub.9C.sub.6 H.sub.4 O H H NOCH.sub.3 139-140335 4-CH.sub.3 ONC(CH.sub.3)C.sub.6 H.sub.4 O H H NOCH.sub.3 79-81336 3,4-Cl.sub.2C.sub.6 H.sub.3 O H H NOCH.sub.3 136-138337 3,5-Cl.sub.2C.sub.6 H.sub.3 O H H NOCH.sub.3 115-116338 2-Phenyloxazol-4-yl- H H NOCH.sub.3 134-135 methoxy339 CH.sub.3 OOCCH.sub.2 O H H NOCH.sub.3 oil 6.50/7.77340 t-C.sub.4 H.sub.9 OOCCH.sub.2 O H H NOCH.sub.3 oil 6.48/7.53341 t-C.sub.4 H.sub.9 NH H H NOCH.sub.3 199-202342 CH.sub.3 OOOCH(CH.sub.3)NH H H NOCH.sub.3343 CH.sub.3 OOCCH(i-C.sub.4 H.sub.9)NH H H NOCH.sub.3344 Piperidin-1-yl H H NOCH.sub.3 122-124345 CH.sub.2C(CH.sub.3)CH.sub.2 ONH H H NOCH.sub.3 133-136346 CH.sub.2CClCH.sub.2 ONH H H NOCH.sub.3347 3',4'-Cl.sub.2C.sub.6 H.sub.3CH.sub.2 ONH H H NOCH.sub.3 119-120348 HO H CH.sub.3 NOCH.sub.3349 2-CH.sub.3C.sub.6 H.sub.4 O H CH.sub.3 NOCH.sub.3350 3-CF.sub.3C.sub.6 H.sub.4 O H CH.sub.3 NOCH.sub.3351 4-ClC.sub.6 H.sub.4 O H CH.sub.3 NOCH.sub.3352 3,5-Cl.sub.2C.sub.6 H.sub.3 O H CH.sub.3 NOCH.sub.3353 i-C.sub.3 H.sub.7 O H H CHOCH.sub.3 75-76354 i-C.sub.3 H.sub.7 O H CH.sub.3 CHOCH.sub.3355 i-C.sub.3 H.sub.7 O H H NOCH.sub.3356 i-C.sub.3 H.sub.7 O H CH.sub.3 NOCH.sub.3__________________________________________________________________________ TABLE II__________________________________________________________________________ ##STR12## m.p.No. Q.sub.m X (.degree.C.) .delta. (CC .sub.--H)__________________________________________________________________________1 3-F CHOCH.sub.32 2,6-F.sub.2 CHOCH.sub.33 2-Cl CHOCH.sub.34 3-Cl CHOCH.sub.35 4-Cl CHOCH.sub.36 2,6-Cl.sub.2 CHOCH.sub.37 3,4-Cl.sub.2 CHOCH.sub.38 3-Br CHOCH.sub.39 4-I CHOCH.sub.310 2-Cl, 6-F CHOCH.sub.311 2-CH.sub.3 CHOCH.sub.312 3-CH.sub.3 CHOCH.sub.313 4-CH.sub.3 CHOCH.sub.314 2,4-(CH.sub.3).sub.2 CHOCH.sub.315 2,4,6-(CH.sub.3).sub.3 CHOCH.sub.316 3-C.sub.2 H.sub.5 CHOCH.sub.317 R-t-C.sub.4 H.sub.9 CHOCH.sub.318 4-Cyclohexyl CHOCH.sub.319 3-CH.sub.2 C.sub.6 H.sub.5 CHOCH.sub.320 2-OCH.sub.3 CHOCH.sub.321 3-OCH.sub.3 CHOCH.sub.322 4-OCH.sub.3 CHOCH.sub.3 Oil 7.50/ 7.8123 2-O-i-C.sub.3 H.sub.7 CHOCH.sub.324 3-OCH.sub.2 C.sub.6 H.sub.5 CHOCH.sub.325 3-CF.sub.3 CHOCH.sub.326 3-NO.sub.2 CHOCH.sub.327 4-NO.sub.2 CHOCH.sub.328 3-Cyano CHOCH.sub.329 2-Cl, 4-CH.sub.3 CHOCH.sub.330 2-COOCH.sub.3 CHOCH.sub.331 4-CH.sub.2 OCH.sub.3 CHOCH.sub.332 4-COCH.sub.3 CHOCH.sub.333 2-CH.sub.3 -4-COCH.sub.3 CHOCH.sub.334 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHOCH.sub.335 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHOCH.sub.336 3-F NOCH.sub.337 2,6-F.sub.2 NOCH.sub.338 2-Cl NOCH.sub.339 3-Cl NOCH.sub.340 4-Cl NOCH.sub.3 104-10741 2,6-Cl.sub.2 NOCH.sub.342 3,4-Cl.sub.2 NOCH.sub.343 3-Br NOCH.sub.344 4-I NOCH.sub.345 2-Cl, 6-F NOCH.sub.346 2-CH.sub.3 NOCH.sub.347 3-CH.sub.3 NOCH.sub.348 4-CH.sub.3 NOCH.sub.349 2,4-(CH.sub.3).sub.2 NOCH.sub.350 2,4,6-(CH.sub.3).sub.3 NOCH.sub.351 3-C.sub.2 H.sub.5 NOCH.sub.352 4-t-C.sub.4 H.sub.9 NOCH.sub.353 4-Cyclohexyl NOCH.sub.354 3-CH.sub.2 C.sub.6 H.sub.5 NOCH.sub.355 2-OCH.sub.3 NOCH.sub.356 3-OCH.sub.3 NOCH.sub.3 98-10257 4-OCH.sub.3 NOCH.sub.3 137-14158 2-O-i-C.sub.3 H.sub.7 NOCH.sub.359 3-OCH.sub.2 C.sub.6 H.sub.5 NOCH.sub.360 3-CF.sub.3 NOCH.sub.361 3-NO.sub.2 NOCH.sub.362 4-NO.sub.2 NOCH.sub.363 3-Cyano NOCH.sub.364 2-Cl, 4-CH.sub.3 NOCH.sub.365 2-COOCH.sub.3 NOCH.sub.366 4-CH.sub.2 OCH.sub.3 NOCH.sub.367 4-COCH.sub.3 NOCH.sub.368 2-CH.sub.3 -4-COCH.sub.3 NOCH.sub.369 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 NOCH.sub.370 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 NOCH.sub.371 3-F CHCH.sub.372 2,6-F.sub.2 CHCH.sub.373 2-Cl CHCH.sub.374 3-Cl CHCH.sub.375 4-Cl CHCH.sub.376 2,6-Cl.sub.2 CHCH.sub.377 3,4-Cl.sub.2 CHCH.sub.378 3-Br CHCH.sub.379 R-I CHCH.sub.380 2-Cl, 6-F CHCH.sub.381 2-CH.sub.3 CHCH.sub.382 3-CH.sub.3 CHCH.sub.383 4-CH.sub.3 CHCH.sub.384 2,4-(CH.sub.3).sub.2 CHCH.sub.385 2,4,6-(CH.sub.3).sub.3 CHCH.sub.386 3-C.sub.2 H.sub.5 CHCH.sub.387 4-t-C.sub.4 H.sub.9 CHCH.sub.388 4-Cyclohexyl CHCH.sub.389 3-CH.sub.2 C.sub.6 H.sub.5 CHCH.sub.390 2-OCH.sub.3 CHCH.sub.391 3-OCH.sub. 3 CHCH.sub.392 4-OCH.sub.3 CHCH.sub.393 2-O-i-C.sub.3 H.sub.7 CHCH.sub.394 3-OCH.sub.2 C.sub.6 H.sub.5 CHCH.sub.395 3-CF.sub.3 CHCH.sub.396 3-NO.sub.2 CHCH.sub.397 4-NO.sub.2 CHCH.sub.398 3-Cyano CHCH.sub.399 2-Cl, 4-CH.sub.3 CHCH.sub.3100 2-COOCH.sub.3 CHCH.sub.3101 4-CH.sub.2 OCH.sub.3 CHCH.sub.3102 4-COCH.sub.3 CHCH.sub.3103 2-CH.sub.3 -4-COCH.sub.3 CHCH.sub.3104 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHCH.sub.3105 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHCH.sub.3106 3-F CHC.sub.2 H.sub.5107 2,6-F.sub.2 CHC.sub.2 H.sub.5108 2-Cl CHC.sub.2 H.sub.5109 3-Cl CHC.sub.2 H.sub.5110 4-Cl CHC.sub.2 H.sub.5111 2,6-Cl.sub.2 CHC.sub.2 H.sub.5112 3,4-Cl.sub.2 CHC.sub.2 H.sub.5113 3-Br CHC.sub.2 H.sub.5114 4-I CHC.sub.2 H.sub.5115 2-Cl, 6-F CHC.sub.2 H.sub.5116 2-CH.sub.3 CHC.sub.2 H.sub.5117 3-CH.sub.3 CHC.sub.2 H.sub.5118 4-CH.sub.3 CHC.sub.2 H.sub.5119 2,4-(CH.sub.3).sub.2 CHC.sub.2 H.sub.5120 2,4,6-(CH.sub.3).sub.3 CHC.sub.2 H.sub.5121 3-C.sub.2 H.sub.5 CHC.sub.2 H.sub.5122 4-t-C.sub.4 H.sub.9 CHC.sub.2 H.sub.5123 4-Cyclohexyl CHC.sub.2 H.sub.5124 3-CH.sub.2 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5125 2-OCH.sub.3 CHC.sub.2 H.sub.5126 3-OCH.sub.3 CHC.sub.2 H.sub.5127 4-OCH.sub.3 CHC.sub.2 H.sub.5128 2-O-i-C.sub.3 H.sub.7 CHC.sub.2 H.sub.5129 3-OCH.sub.2 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5130 3-CF.sub.3 CHC.sub.2 H.sub.5131 3-NO.sub.2 CHC.sub.2 H.sub.5132 4-NO.sub.2 CHC.sub.2 H.sub.5133 3-Cyano CHC.sub.2 H.sub.5134 2-Cl, 4-CH.sub.3 CHC.sub.2 H.sub.5135 2-COOCH.sub.3 CHC.sub.2 H.sub.5136 4-CH.sub.2 OCH.sub.3 CHC.sub.2 H.sub.5137 4-COCH.sub.3 CHC.sub.2 H.sub.5138 2-CH.sub.3 -4-COCH.sub.3 CHC.sub.2 H.sub.5139 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHC.sub.2 H.sub.5140 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHC.sub.2 H.sub.5__________________________________________________________________________ TABLE III__________________________________________________________________________ ##STR13## m.p.No. Q.sub.m X (.degree.C.) .delta. (CC .sub.--H)__________________________________________________________________________1 3-F CHOCH.sub.32 2,6-F.sub.29 CHOCH.sub.3 114-1163 2-Cl CHOCH.sub.34 3-Cl CHOCH.sub.35 4-Cl CHOCH.sub.36 2,6-Cl.sub.2 CHOCH.sub.37 3,4-Cl.sub.2 CHOCH.sub.38 3-Br CHOCH.sub.39 4-I CHOCH.sub.310 2-Cl, 6-F CHOCH.sub.311 2-CH.sub.3 CHOCH.sub.3 110-11212 3-CH.sub.3 CHOCH.sub.3 oil 6.44/ 6.7313 4-CH.sub.3 CHOCH.sub.314 2,4-(CH.sub.3).sub.2 CHOCH.sub.315 2,4,6-(CH.sub.3).sub.3 CHOCH.sub.316 3-C.sub.2 H.sub.5 CHOCH.sub.317 4-t-C.sub.4 H.sub.9 CHOCH.sub.318 4-Cyclohexyl CHOCH.sub.319 3-CH.sub.2 C.sub.6 H.sub.5 CHOCH.sub.320 2-OCH.sub.3 CHOCH.sub.321 3-OCH.sub.3 CHOCH.sub.322 4-OCH.sub.3 CHOCH.sub. 323 2-O-i-C.sub.3 H.sub.7 CHOCH.sub.324 3-OCH.sub.2 C.sub.6 H.sub.5 CHOCH.sub.325 3-CF.sub.3 CHOCH.sub.326 3-NO.sub.2 CHOCH.sub.327 2-Cyano CHOCH.sub.3 141-14228 3-Cyano CHOCH.sub.3 93-9429 2-Cl, 4-CH.sub.3 CHOCH.sub.330 2-COOCH.sub.3 CHOCH.sub.331 4-CH.sub.2 OCH.sub.3 CHOCH.sub.332 4-COCH.sub.3 CHOCH.sub.333 2-CH.sub.3 -4-COCH.sub.3 CHOCH.sub.334 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHOCH.sub.335 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHOCH.sub.336 3-F NOCH.sub.337 2,6-F.sub.2 NOCH.sub.3 108-11038 2-Cl NOCH.sub.339 3-Cl NOCH.sub.340 4-Cl NOCH.sub.341 2,6-Cl.sub.2 NOCH.sub.342 3,4-Cl.sub.2 NOCH.sub.343 3-Br NOCH.sub.344 4-I NOCH.sub.345 2-Cl, 6-F NOCH.sub.346 2-CH.sub.3 NOCH.sub.3 91-9447 3-CH.sub.3 NOCH.sub.3 oil 6.45/ 7.5148 4-CH.sub.3 NOCH.sub.349 2,4-(CH.sub.3).sub.2 NOCH.sub.350 2,4,6-(CH.sub.3).sub.3 NOCH.sub.351 3-C.sub.2 H.sub.5 NOCH.sub.352 4-t-C.sub.4 H.sub.9 NOCH.sub.353 4-Cyclohexyl NOCH.sub.354 3-CH.sub.2 C.sub.6 H.sub.5 NOCH.sub.355 2-OCH.sub.3 NOCH.sub.3 87-8856 3-OCH.sub.3 NOCH.sub.357 4-OCH.sub.3 NOCH.sub.358 2-O-i-C.sub.3 H.sub.7 NOCH.sub.359 3-OCH.sub.2 C.sub.6 H.sub.5 NOCH.sub.360 3-CF.sub.3 NOCH.sub.361 3-NO.sub.2 NOCH.sub.362 2-Cyano NOCH.sub.3 127-12963 3-Cyano NOCH.sub.3 104-10664 2-Cl, 4-CH.sub.3 NOCH.sub.365 2-COOCH.sub.3 NOCH.sub.366 4-CH.sub.2 OCH.sub.3 NOCH.sub.367 4-COCH.sub.3 NOCH.sub.368 2-CH.sub.3 -4-COCH.sub.3 NOCH.sub.369 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 NOCH.sub.370 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 NOCH.sub.371 3-F CHCH.sub.372 2,6-F.sub.2 CHCH.sub.373 2-Cl CHCH.sub.374 3-Cl CHCH.sub.375 4-Cl CHCH.sub.376 2,6-Cl.sub.2 CHCH.sub.377 3,4-Cl.sub.2 CHCH.sub.378 3-Br CHCH.sub.379 4-I CHCH.sub.380 2-Cl, 6-F CHCH.sub.381 2-CH.sub.3 CHCH.sub.382 3-CH.sub.3 CHCH.sub.383 4-CH.sub.3 CHCH.sub.384 2,4-(CH.sub.3).sub.2 CHCH.sub.385 2,4,6-(CH.sub.3).sub.3 CHCH.sub.386 3-C.sub.2 H.sub.5 CHCH.sub.387 4-t-C.sub.4 H.sub.9 CHCH.sub.388 4-Cyclohexyl CHCH.sub.389 3-CH.sub.2 C.sub.6 H.sub.5 CHCH.sub.390 2-OCH.sub.3 CHCH.sub.391 3-OCH.sub.3 CHCH.sub.392 4-OCH.sub.3 CHCH.sub.393 2-O-i-C.sub.3 H.sub.7 CHCH.sub.394 3-OCH.sub.2 C.sub.6 H.sub.5 CHCH.sub.395 3-CF.sub.3 CHCH.sub.396 3-NO.sub.2 CHCH.sub.397 2-Cyano CHCH.sub.398 3-Cyano CHCH.sub.399 2-Cl, 4-CH.sub.3 CHCH.sub.3100 2-COOCH.sub.3 CHCH.sub.3101 4-CH.sub.2 OCH.sub.3 CHCH.sub.3102 4-COCH.sub.3 CHCH.sub.3103 2-CH.sub.3 -4-COCH.sub.3 CHCH.sub.3104 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHCH.sub.3105 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHCH.sub.3106 3-F CHC.sub.2 H.sub.5107 2,6-F.sub.2 CHC.sub.2 H.sub.5108 2-Cl CHC.sub.2 H.sub.5109 3-Cl CHC.sub.2 H.sub.5110 4-Cl CHC.sub.2 H.sub.5111 2,6-Cl.sub.2 CHC.sub.2 H.sub.5112 3,4-Cl.sub.2 CHC.sub.2 H.sub.5113 3-Br CHC.sub.2 H.sub.5114 4-I CHC.sub.2 H.sub.5115 2-Cl, 6-F CHC.sub.2 H.sub.5116 2-CH.sub.3 CHC.sub.2 H.sub.5117 3-CH.sub.3 CHC.sub.2 H.sub.5118 4-CH.sub.3 CHC.sub.2 H.sub. 5119 2,4-(CH.sub.3).sub.2 CHC.sub.2 H.sub.5120 2,4,6-(CH.sub.3).sub.3 CHC.sub.2 H.sub.5121 3-C.sub.2 H.sub.5 CHC.sub.2 H.sub.5122 4-t-C.sub.4 H.sub.9 CHC.sub.2 H.sub.5123 4-Cyclohexyl CHC.sub.2 H.sub.5124 3-CH.sub.2 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5125 2-OCH.sub.3 CHC.sub.2 H.sub.5126 3-OCH.sub.3 CHC.sub.2 H.sub.5127 4-OCH.sub.3 CHC.sub.2 H.sub.5128 2-O-i-C.sub.3 H.sub.7 CHC.sub.2 H.sub.5129 3-OCH.sub.2 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5130 3-CF.sub.3 CHC.sub.2 H.sub.5131 3-NO.sub.2 CHC.sub.2 H.sub.5132 2-Cyano CHC.sub.2 H.sub.5133 3-Cyano CHC.sub.2 H.sub.5134 2-Cl, 4-CH.sub.3 CHC.sub.2 H.sub.5135 2-COOCH.sub.3 CHC.sub.2 H.sub.5136 4-CH.sub.2 OCH.sub.3 CHC.sub.2 H.sub.5137 4-COCH.sub.3 CHC.sub.2 H.sub.5138 2-CH.sub.3 -4-COCH.sub.3 CHC.sub.2 H.sub.5139 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHC.sub.2 H.sub.5140 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CHC.sub.2 H.sub.5__________________________________________________________________________ TABLE IV__________________________________________________________________________ ##STR14## m.p.No. Q.sub.m R X (.degree.C.) .delta. (CC .sub.-- H)__________________________________________________________________________ 1 3-F H CHOCH.sub.3 165-168 2 2,6-F.sub.2 H CHOCH.sub.3 3 2-Cl H CHOCH.sub.3 4 3-Cl H CHOCH.sub.3 5 4-Cl H CHOCH.sub.3 6 2,6-Cl.sub.2 H CHOCH.sub.3 7 3,4-Cl.sub.2 H CHOCH.sub.3 8 3-Br H CHOCH.sub.3 9 4-I H CHOCH.sub.3 10 2-Cl, 6-F H CHOCH.sub.3 11 2-CH.sub.3 H CHOCH.sub.3 12 3-CH.sub.3 H CHOCH.sub.3 150-152 13 4-CH.sub.3 H CHOCH.sub.3 14 2,4-(CH.sub.3).sub.2 H CHOCH.sub.3 15 2,4,6-(CH.sub.3).sub.3 H CHOCH.sub.3 16 3-C.sub.2 H.sub.5 H CHOCH.sub.3 17 4-t-C.sub.4 H.sub.9 H CHOCH.sub.3 18 4-Cyclohexyl H CHOCH.sub.3 19 3-CH.sub.2 C.sub.6 H.sub.5 H CHOCH.sub.3 20 2-OCH.sub.3 H CHOCH.sub.3 21 3-OCH.sub.3 H CHOCH.sub.3 22 4-OCH.sub.3 H CHOCH.sub.3 23 2-O-i-C.sub.3 H.sub.7 H CHOCH.sub.3 24 3-OCH.sub.2 C.sub.6 H.sub.5 H CHOCH.sub.3 25 3-CF.sub.3 H CHOCH.sub.3 26 3-NO.sub.2 H CHOCH.sub.3 27 4-NO.sub.2 H CHOCH.sub.3 28 3-Cyano H CHOCH.sub.3 29 2-Cl, 4-CH.sub.3 H CHOCH.sub.3 30 2-COOCH.sub.3 H CHOCH.sub.3 140-143 31 4-CH.sub.2 OCH.sub.3 H CHOCH.sub.3 32 4-COCH.sub.3 H CHOCH.sub.3 33 2-CH.sub.3 -4-COCH.sub.3 H CHOCH.sub.3 34 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHOCH.sub.3 35 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHOCH.sub.3 36 3-F CH.sub.3 CHOCH.sub.3 37 2,6-F.sub.2 CH.sub.3 CHOCH.sub.3 38 2-Cl CH.sub.3 CHOCH.sub.3 39 3-Cl CH.sub.3 CHOCH.sub.3 40 4-Cl CH.sub.3 CHOCH.sub.3 41 2,6-Cl.sub.2 CH.sub.3 CHOCH.sub.3 42 3,4-Cl.sub.2 CH.sub.3 CHOCH.sub.3 43 3-Br CH.sub.3 CHOCH.sub.3 44 4-I CH.sub.3 CHOCH.sub.3 45 2-Cl, 6-F CH.sub.3 CHOCH.sub.3 46 2-CH.sub.3 CH.sub.3 CHOCH.sub.3 47 3-CH.sub.3 CH.sub.3 CHOCH.sub.3 48 4-CH.sub.3 CH.sub.3 CHOCH.sub.3 49 2,4-(CH.sub.3).sub.2 CH.sub.3 CHOCH.sub.3 50 2,4,6-(CH.sub.3).sub.3 CH.sub.3 CHOCH.sub.3 51 3-C.sub.2 H.sub.5 CH.sub.3 CHOCH.sub.3 52 4-t-C.sub.4 H.sub.9 CH.sub.3 CHOCH.sub.3 53 4-Cyclohexyl CH.sub.3 CHOCH.sub.3 54 3-CH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHOCH.sub.3 55 2-OCH.sub.3 CH.sub.3 CHOCH.sub.3 56 3-OCH.sub.3 CH.sub.3 CHOCH.sub.3 57 4-OCH.sub.3 CH.sub.3 CHOCH.sub.3 58 2-O-i-C.sub.3 H.sub.7 CH.sub.3 CHOCH.sub.3 59 3-OCH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHOCH.sub.3 60 3-CF.sub.3 CH.sub.3 CHOCH.sub.3 61 3-NO.sub.2 CH.sub.3 CHOCH.sub.3 62 4-NO.sub.2 CH.sub.3 CHOCH.sub.3 63 3-Cyano CH.sub.3 CHOCH.sub.3 64 2-Cl, 4-CH.sub.3 CH.sub.3 CHOCH.sub.3 65 2-COOCH.sub.3 CH.sub.3 CHOCH.sub.3 66 4-CH.sub.2 OCH.sub.3 CH.sub.3 CHOCH.sub.3 67 4-COCH.sub.3 CH.sub.3 CHOCH.sub.3 68 2-CH.sub.3 -4-COCH.sub.3 CH.sub.3 CHOCH.sub.3 69 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHOCH.sub.3 70 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHOCH.sub.3 71 3-F H NOCH.sub.3 138-141 72 2,6-F.sub.2 H NOCH.sub.3 73 2-Cl H NOCH.sub.3 74 3-Cl H NOCH.sub.3 75 4-Cl H NOCH.sub.3 76 2,6-Cl.sub.2 H NOCH.sub.3 77 3,4-Cl.sub.2 H NOCH.sub.3 78 3-Br H NOCH.sub.3 79 4-I H NOCH.sub.3 80 2-Cl, 6-F H NOCH.sub.3 81 2-CH.sub.3 H NOCH.sub.3 82 3-CH.sub.3 H NOCH.sub.3 125-127 83 4-CH.sub.3 H NOCH.sub.3 84 2,4-(CH.sub.3).sub.2 H NOCH.sub.3 85 2,4,6-(CH.sub.3).sub.3 H NOCH.sub.3 86 3-C.sub.2 H.sub.5 H NOCH.sub.3 87 4-t-C.sub.4 H.sub.9 H NOCH.sub.3 88 4-Cyclohexyl H NOCH.sub.3 89 3-CH.sub.2 C.sub.6 H.sub.5 H NOCH.sub.3 90 2-OCH.sub.3 H NOCH.sub.3 91 3-OCH.sub.3 H NOCH.sub.3 92 4-OCH.sub.3 H NOCH.sub.3 93 2-O-i-C.sub.3 H.sub.7 H NOCH.sub.3 94 3-OCH.sub.2 C.sub.6 H.sub.5 H NOCH.sub.3 95 3-CF.sub.3 H NOCH.sub.3 96 3-NO.sub.2 H NOCH.sub.3 97 4-NO.sub.2 H NOCH.sub.3 98 3-Cyano H NOCH.sub.3 99 2-Cl, 4-CH.sub.3 H NOCH.sub.3100 2-COOCH.sub.3 H NOCH.sub.3 165 (de- comp.)101 4-CH.sub.2 OCH.sub.3 H NOCH.sub.3102 4-COCH.sub.3 H NOCH.sub.3103 2-CH.sub.3 -4-COCH.sub.3 H NOCH.sub.3104 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H NOCH.sub.3105 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H NOCH.sub.3106 3-F CH.sub.3 NOCH.sub.3107 2,6-F.sub.2 CH.sub.3 NOCH.sub.3108 2-Cl CH.sub.3 NOCH.sub.3109 3-Cl CH.sub.3 NOCH.sub.3110 4-Cl CH.sub.3 NOCH.sub.3111 2,6-Cl.sub.2 CH.sub.3 NOCH.sub.3112 3,4-Cl.sub.2 CH.sub.3 NOCH.sub.3113 3-Br CH.sub.3 NOCH.sub.3114 4-I CH.sub.3 NOCH.sub.3115 2-Cl, 6-F CH.sub.3 NOCH.sub.3116 2-CH.sub.3 CH.sub.3 NOCH.sub.3117 3-CH.sub.3 CH.sub.3 NOCH.sub.3118 4-CH.sub.3 CH.sub.3 NOCH.sub.3119 2,4-(CH.sub.3).sub.2 CH.sub.3 NOCH.sub.3120 2,4,6-(CH.sub.3).sub.3 CH.sub.3 NOCH.sub.3121 3-C.sub.2 H.sub.5 CH.sub.3 NOCH.sub.3122 4-t-C.sub.4 H.sub.9 CH.sub.3 NOCH.sub.3123 4-Cyclohexyl CH.sub.3 NOCH.sub.3124 3-CH.sub.2 C.sub.6 H.sub.5 CH.sub.3 NOCH.sub.3125 2-OCH.sub.3 CH.sub.3 NOCH.sub.3126 3-OCH.sub.3 CH.sub.3 NOCH.sub.3127 4-OCH.sub.3 CH.sub.3 NOCH.sub.3128 2-O-i-C.sub.3 H.sub.7 CH.sub.3 NOCH.sub.3129 3-OCH.sub.2 C.sub.6 H.sub.5 CH.sub.3 NOCH.sub.3130 3-CF.sub.3 CH.sub.3 NOCH.sub.3131 3-NO.sub.2 CH.sub.3 NOCH.sub.3132 4-NO.sub.2 CH.sub.3 NOCH.sub.3133 3-Cyano CH.sub.3 NOCH.sub.3134 2-Cl, 4-CH.sub.3 CH.sub.3 NOCH.sub.3135 2-COOCH.sub.3 CH.sub.3 NOCH.sub.3136 4-CH.sub.2 OCH.sub.3 CH.sub.3 NOCH.sub.3137 4-COCH.sub.3 CH.sub.3 NOCH.sub.3138 2-CH.sub.3 -4-COCH.sub.3 CH.sub.3 NOCH.sub.3139 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 NOCH.sub. 3140 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 NOCH.sub.3141 3-F H CHCH.sub.3142 2,6-F.sub.2 H CHCH.sub.3143 2-Cl H CHCH.sub.3144 3-Cl H CHCH.sub.3145 4-Cl H CHCH.sub.3146 2,6-Cl.sub.2 H CHCH.sub.3147 3,4-Cl.sub.2 H CHCH.sub.3148 3-Br H CHCH.sub.3149 4-I H CHCH.sub.3150 2-Cl, 6-F H CHCH.sub.3151 2-CH.sub.3 H CHCH.sub.3152 3-CH.sub.3 H CHCH.sub.3153 4-CH.sub.3 H CHCH.sub.3154 2,4-(CH.sub.3).sub.2 H CHCH.sub.3155 2,4,6-(CH.sub.3).sub.3 H CHCH.sub.3156 3-C.sub.2 H.sub.5 H CHCH.sub.3157 4-t-C.sub.4 H.sub.9 H CHCH.sub.3158 4-Cyclohexyl H CHCH.sub.3159 3-CH.sub.2 C.sub.6 H.sub.5 H CHCH.sub.3160 2-OCH.sub.3 H CHCH.sub.3161 3-OCH.sub.3 H CHCH.sub.3162 4-OCH.sub.3 H CHCH.sub.3163 2-O-i-C.sub.3 H.sub.7 H CHCH.sub.3164 3-OCH.sub.2 C.sub.6 H.sub.5 H CHCH.sub.3165 3-CF.sub.3 H CHCH.sub.3166 3-NO.sub.2 H CHCH.sub.3167 4-NO.sub.2 H CHCH.sub.3168 3-Cyano H CHCH.sub.3169 2-Cl, 4-CH.sub.3 H CHCH.sub. 3170 2-COOCH.sub.3 H CHCH.sub.3171 4-CH.sub.2 OCH.sub.3 H CHCH.sub.3172 4-COCH.sub.3 H CHCH.sub.3173 2-CH.sub.3 -4-COCH.sub.3 H CHCH.sub.3174 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHCH.sub.3175 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHCH.sub.3176 3-F CH.sub.3 CHCH.sub.3177 2,6-F.sub.2 CH.sub.3 CHCH.sub.3178 2-Cl CH.sub.3 CHCH.sub.3179 3-Cl CH.sub.3 CHCH.sub.3180 4-Cl CH.sub.3 CHCH.sub.3181 2,6-Cl.sub.2 CH.sub.3 CHCH.sub.3182 3,4-Cl.sub.2 CH.sub.3 CHCH.sub.3183 3-Br CH.sub.3 CHCH.sub.3184 4-I CH.sub.3 CHCH.sub.3185 2-Cl, 6-F CH.sub.3 CHCH.sub.3186 2-CH.sub.3 CH.sub.3 CHCH.sub.3187 3-CH.sub.3 CH.sub.3 CHCH.sub.3188 4-CH.sub.3 CH.sub.3 CHCH.sub.3189 2,4-(CH.sub.3).sub.2 CH.sub.3 CHCH.sub.3190 2,4,6-(CH.sub.3).sub.3 CH.sub.3 CHCH.sub.3191 3-C.sub.2 H.sub.5 CH.sub.3 CHCH.sub.3192 4-t-C.sub.4 H.sub.9 CH.sub.3 CHCH.sub.3193 4-Cyclohexyl CH.sub.3 CHCH.sub.3194 3-CH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHCH.sub.3195 2-OCH.sub.3 CH.sub.3 CHCH.sub.3196 3-OCH.sub.3 CH.sub.3 CHCH.sub.3197 4-OCH.sub.3 CH.sub.3 CHCH.sub.3198 2-O-i-C.sub.3 H.sub.7 CH.sub.3 CHCH.sub.3199 3-OCH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHCH.sub.3200 3-CF.sub.3 CH.sub.3 CHCH.sub.3201 3-NO.sub.2 CH.sub.3 CHCH.sub.3202 4-NO.sub.2 CH.sub.3 CHCH.sub.3203 3-Cyano CH.sub.3 CHCH.sub.3204 2-Cl, 4-CH.sub.3 CH.sub.3 CHCH.sub.3205 2-COOCH.sub.3 CH.sub.3 CHCH.sub.3206 4-CH.sub.2 OCH.sub.3 CH.sub.3 CHCH.sub.3207 4-COCH.sub.3 CH.sub.3 CHCH.sub.3208 2-CH.sub.3 -4-COCH.sub.3 CH.sub.3 CHCH.sub.3209 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHCH.sub.3210 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHCH.sub.3211 3-F H CHC.sub.2 H.sub.5212 2,6-F.sub.2 H CHC.sub.2 H.sub.5213 2-Cl H CHC.sub.2 H.sub.5214 3-Cl H CHC.sub.2 H.sub.5215 4-Cl H CHC.sub.2 H.sub.5216 2,6-Cl.sub.2 H CHC.sub.2 H.sub.5217 3,4-Cl.sub.2 H CHC.sub.2 H.sub.5218 3-Br H CHC.sub.2 H.sub.5219 4-I H CHC.sub.2 H.sub.5220 2-Cl, 6-F H CHC.sub.2 H.sub. 5221 2-CH.sub.3 H CHC.sub.2 H.sub.5222 3-CH.sub.3 H CHC.sub.2 H.sub.5223 4-CH.sub.3 H CHC.sub.2 H.sub.5224 2,4-(CH.sub.3).sub.2 H CHC.sub.2 H.sub.5225 2,4,6-(CH.sub.3).sub.3 H CHC.sub.2 H.sub.5226 3-C.sub.2 H.sub.5 H CHC.sub.2 H.sub.5227 4-t-C.sub.4 H.sub.9 H CHC.sub.2 H.sub.5228 4-Cyclohexyl H CHC.sub.2 H.sub.5229 3-CH.sub.2 C.sub.6 H.sub.5 H CHC.sub.2 H.sub.5230 2-OCH.sub.3 H CHC.sub.2 H.sub.5231 3-OCH.sub.3 H CHC.sub.2 H.sub.5232 4-OCH.sub.3 H CHC.sub.2 H.sub.5233 2-O-i-C.sub.3 H.sub.7 H CHC.sub.2 H.sub.5234 3-OCH.sub.2 C.sub.6 H.sub.5 H CHC.sub.2 H.sub.5235 3-CF.sub.3 H CHC.sub.2 H.sub.5236 3-NO.sub.2 H CHC.sub.2 H.sub.5237 4-NO.sub.2 H CHC.sub.2 H.sub.5238 3-Cyano H CHC.sub.2 H.sub.5239 2-Cl, 4-CH.sub.3 H CHC.sub.2 H.sub.5240 2-COOCH.sub.3 H CHC.sub.2 H.sub.5241 4-CH.sub.2 OCH.sub.3 H CHC.sub.2 H.sub.5242 4-COCH.sub.3 H CHC.sub.2 H.sub.5243 2-CH.sub.3 -4-COCH.sub. 3 H CHC.sub.2 H.sub.5244 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHC.sub.2 H.sub.5245 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHC.sub.2 H.sub.5246 3-F CH.sub.3 CHC.sub.2 H.sub.5247 2,6-F.sub.2 CH.sub.3 CHC.sub.2 H.sub.5248 2-Cl CH.sub.3 CHC.sub.2 H.sub.5249 3-Cl CH.sub.3 CHC.sub.2 H.sub.5250 4-Cl CH.sub.3 CHC.sub.2 H.sub.5251 2,6-Cl.sub.2 CH.sub.3 CHC.sub.2 H.sub.5252 3,4-Cl.sub.2 CH.sub.3 CHC.sub.2 H.sub.5253 3-Br CH.sub.3 CHC.sub.2 H.sub.5254 4-I CH.sub.3 CHC.sub.2 H.sub.5255 2-Cl, 6-F CH.sub.3 CHC.sub.2 H.sub.5256 2-CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5257 3-CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5258 4-CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5259 2,4-(CH.sub.3).sub.2 CH.sub.3 CHC.sub.2 H.sub.5260 2,4,6-(CH.sub.3).sub.3 CH.sub.3 CHC.sub.2 H.sub.5261 3-C.sub.2 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5262 4-t-C.sub.4 H.sub.9 CH.sub.3 CHC.sub.2 H.sub.5263 4-Cyclohexyl CH.sub.3 CHC.sub.2 H.sub.5264 2-CH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5265 2-OCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5266 3-OCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5267 4-OCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5268 2-O-i-C.sub.3 H.sub.7 CH.sub.3 CHC.sub.2 H.sub.5269 3-OCH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5270 3-CF.sub.3 CH.sub.3 CHC.sub.2 H.sub.5271 3-NO.sub.2 CH.sub.3 CHC.sub.2 H.sub.5272 4-NO.sub.2 CH.sub.3 CHC.sub.2 H.sub.5273 3-Cyano CH.sub.3 CHC.sub.2 H.sub.5274 2-Cl, 4-CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5275 2-COOCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5276 4-CH.sub.2 OCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5277 4-COCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5278 2-CH.sub.3 -4-COCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5279 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5280 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5__________________________________________________________________________ TABLE V______________________________________ ##STR15## Iso- m.p. .delta.No. R A X mer (.degree.C.) (CC .sub.--H)______________________________________1 CH.sub.3 H CHOCH.sub.32 t-C.sub.4 H.sub.9 H CHOCH.sub.33 C.sub.6 H.sub.5 H CHOCH.sub.34 2-ClC.sub.6 H.sub.4 H CHOCH.sub.35 3-ClC.sub.6 H.sub.4 H CHOCH.sub.36 4-ClC.sub.6 H.sub.4 H CHOCH.sub.37 2-CH.sub.3 C.sub.6 H.sub.4 H CHOCH.sub.38 3-CH.sub.3 OC.sub.6 H.sub.4 H CHOCH.sub.39 4-Cyano-C.sub.6 H.sub.4 H CHOCH.sub.310 2,6-F.sub.2C.sub.6 H.sub.3 H CHOCH.sub.311 3-Pyridyl H CHOCH.sub.312 2-Furyl H CHOCH.sub.313 .beta.-Naphthyl H CHOCH.sub.314 CH.sub.3 CH.sub.3 CHOCH.sub.315 t-C.sub.4 H.sub.9 CH.sub.3 CHOCH.sub.316 C.sub.6 H.sub.5 CH.sub.3 CHOCH.sub.317 2-ClC.sub.6 H.sub.4 CH.sub.3 CHOCH.sub.318 3-ClC.sub.6 H.sub.4 CH.sub.3 CHOCH.sub.319 4-ClC.sub.6 H.sub.4 CH.sub.3 CHOCH.sub.320 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CHOCH.sub.321 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 CHOCH.sub.322 4-Cyano-C.sub.6 H.sub.4 CH.sub.3 CHOCH.sub.323 2,6-F.sub.2C.sub.6 H.sub.3 CH.sub.3 CHOCH.sub.324 3-Pyridyl CH.sub.3 CHOCH.sub.325 2-Furyl CH.sub.3 CHOCH.sub.326 .beta.-Napththyl CH.sub.3 CHOCH.sub.327 CH.sub.3 C.sub.6 H.sub.5 CHOCH.sub.328 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CHOCH.sub.329 2-CH.sub.3 C.sub.6 H.sub.4 C.sub.6 H.sub.5 CHOCH.sub.330 2,6-F.sub.2 C.sub.6 H.sub.3 C.sub.6 H.sub.5 CHOCH.sub.331 CH.sub.3 H NOCH.sub.332 t-C.sub.4 H.sub.9 H NOCH.sub.333 C.sub.6 H.sub.5 H NOCH.sub.334 2-ClC.sub.6 H.sub.4 H NOCH.sub.335 3-ClC.sub.6 H.sub.4 H NOCH.sub.336 4-ClC.sub.6 H.sub.4 H NOCH.sub.337 2-CH.sub.3 C.sub.6 H.sub.4 H NOCH.sub.338 3-CH.sub.3 OC.sub.6 H.sub. 4 H NOCH.sub.339 4-Cyano-C.sub.6 H.sub.4 H NOCH.sub.340 2,6-F.sub.2C.sub.6 H.sub.3 H NOCH.sub.341 3-Pyridyl H NOCH.sub.342 2-Furyl H NOCH.sub.343 .beta.-Naphthyl H NOCH.sub.344 CH.sub.3 CH.sub.3 NOCH.sub.345 t-C.sub.4 H.sub.9 CH.sub.3 NOCH.sub.346 C.sub.6 H.sub.5 CH.sub.3 NOCH.sub.347 2-ClC.sub.6 H.sub.4 CH.sub.3 NOCH.sub.348 3-ClC.sub.6 H.sub.4 CH.sub.3 NOCH.sub.349 4-ClC.sub.6 H.sub.4 CH.sub.3 NOCH.sub.350 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 NOCH.sub.351 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 NOCH.sub.352 4-Cyano-C.sub.6 H.sub.4 CH.sub.3 NOCH.sub.353 2,6-F.sub.2C.sub.6 H.sub.3 CH.sub.3 NOCH.sub.354 3-Pyridyl CH.sub.3 NOCH.sub.355 2-Furyl CH.sub.3 NOCH.sub.356 .beta.-Naphthyl CH.sub.3 NOCH.sub.357 CH.sub.3 C.sub.6 H.sub.5 NOCH.sub.358 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NOCH.sub.359 2-CH.sub.3 C.sub.6 H.sub.4 C.sub.6 H.sub.5 NOCH.sub.360 2,6-F.sub.2 C.sub.6 H.sub.3 C.sub.6 H.sub.5 NOCH.sub.361 CH.sub.3 H CHCH.sub.362 t-C.sub.4 H.sub.9 H CHCH.sub.363 C.sub.6 H.sub.5 H CHCH.sub.364 2-ClC.sub.6 H.sub.4 H CHCH.sub.365 3-ClC.sub.6 H.sub.4 H CHCH.sub.366 4-ClC.sub.6 H.sub.4 H CHCH.sub.367 2-CH.sub.3 C.sub.6 H.sub.4 H CHCH.sub.368 3-CH.sub.3 OC.sub.6 H.sub.4 H CHCH.sub.369 4-Cyano-C.sub.6 H.sub.4 H CHCH.sub.370 2,6-F.sub.2C.sub.6 H.sub.3 H CHCH.sub.371 3-Pyridyl H CHCH.sub.372 2-Furyl H CHCH.sub.373 .beta.-Napththyl H CHCH.sub.374 CH.sub.3 CH.sub.3 CHCH.sub.375 t-C.sub.4 H.sub.9 CH.sub.3 CHCH.sub.376 C.sub.6 H.sub.5 CH.sub.3 CHCH.sub.377 2-ClC.sub.6 H.sub.4 CH.sub.3 CHCH.sub.378 3-ClC.sub.6 H.sub.4 CH.sub.3 CHCH.sub.379 4-ClC.sub.6 H.sub.4 CH.sub.3 CHCH.sub.380 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CHCH.sub.381 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 CHCH.sub.382 4-Cyano-C.sub.6 H.sub.4 CH.sub.3 CHCH.sub.383 2,6-F.sub.2C.sub.6 H.sub.3 CH.sub.3 CHCH.sub.384 3-Pyridyl CH.sub.3 CHCH.sub.385 2-Furyl CH.sub. 3 CHCH.sub.386 .beta.-Napththyl CH.sub.3 CHCH.sub.387 CH.sub.3 C.sub.6 H.sub.5 CHCH.sub.388 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CHCH.sub.389 2-CH.sub.3 C.sub.6 H.sub.4 C.sub.6 H.sub.5 CHCH.sub.390 2,6-F.sub.2 C.sub.6 H.sub.3 C.sub.6 H.sub.5 CHCH.sub.391 CH.sub.3 H CHC.sub.2 H.sub.592 t-C.sub.4 H.sub.9 H CHC.sub.2 H.sub.593 C.sub.6 H.sub.5 H CHC.sub.2 H.sub.594 2-ClC.sub.6 H.sub.4 H CHC.sub.2 H.sub.595 3-ClC.sub.6 H.sub.4 H CHC.sub.2 H.sub.596 4-ClC.sub.6 H.sub.4 H CHC.sub.2 H.sub.597 2-CH.sub.3 C.sub.6 H.sub.4 H CHC.sub.2 H.sub.598 3-CH.sub.3 OC.sub.6 H.sub.4 H CHC.sub.2 H.sub.599 4-Cyano-C.sub.6 H.sub.4 H CHC.sub.2 H.sub.5100 2,6-F.sub.2C.sub.6 H.sub.3 H CHC.sub.2 H.sub.5101 3-Pyridyl H CHC.sub.2 H.sub.5102 2-Furyl H CHC.sub.2 H.sub.5103 .beta.-Napththyl H CHC.sub.2 H.sub.5104 CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5105 t-C.sub.4 H.sub.9 CH.sub.3 CHC.sub.2 H.sub.5106 C.sub.6 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5107 2-ClC.sub.6 H.sub.4 CH.sub.3 CHC.sub.2 H.sub.5108 3-ClC.sub.6 H.sub.4 CH.sub.3 CHC.sub.2 H.sub.5109 4-ClC.sub.6 H.sub.4 CH.sub.3 CHC.sub.2 H.sub.5110 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CHC.sub.2 H.sub.5111 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 CHC.sub.2 H.sub.5112 4-Cyano-C.sub.6 H.sub.4 CH.sub.3 CHC.sub.2 H.sub.5113 2,6-F.sub.2C.sub.6 H.sub.3 CH.sub.3 CHC.sub.2 H.sub.5114 3-Pyridyl CH.sub.3 CHC.sub.2 H.sub.5115 2-Furyl CH.sub.3 CHC.sub.2 H.sub.5116 .beta.-Naphthyl CH.sub.3 CHC.sub.2 H.sub.5117 CH.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5118 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5119 2-CH.sub.3 C.sub.6 H.sub.4 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5120 2,6-F.sub.2 C.sub.6 H.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5______________________________________ TABLE VI__________________________________________________________________________ ##STR16## Iso- m.p.No. R A X mer (.degree.C.) .delta.(CC .sub.--H)__________________________________________________________________________ 1 H H CHOCH.sub.3 2 CH.sub.3 H CHOCH.sub.3 3 C.sub.2 H.sub.5 H CHOCH.sub.3 4 i-C.sub.3 H.sub.7 H CHOCH.sub.3 5 t-C.sub.4 H.sub.9 H CHOCH.sub.3 6 H.sub.2 CCHCH.sub.2 H CHOCH.sub.3 7 H.sub.2 CCClCH.sub.2 H CHOCH.sub.3 8 CH.sub.3CClCHCH.sub.2 H CHOCH.sub.3 9 HCCCH.sub.2 H CHOCH.sub.3 10 Cyclopropyl H CHOCH.sub.3 11 C.sub.6 H.sub.5 H CHOCH.sub.3 12 4-Pyridyl H CHOCH.sub.3 13 C.sub.6 H.sub. 5 CH.sub.2 H CHOCH.sub.3 14 2-Pyridylmethyl H CHOCH.sub.3 15 5-Chlorothien- H CHOCH.sub.3 2-ylmethyl 16 CH.sub.3 CO H CHOCH.sub.3 17 C.sub.6 H.sub.5 CO H CHOCH.sub.3 18 2-Furyl-CO H CHOCH.sub.3 19 CH.sub.3 OOCCH.sub.2 H CHOCH.sub.3 20 NCCH.sub.2 H CHOCH.sub.3 21 H CH.sub.3 CHOCH.sub.3 a oil 6.70/6.86 s oil 6.93/6.54 22 CH.sub.3 CH.sub.3 CHOCH.sub.3 a oil both 6.81 s oil 6.90/7.42 23 C.sub.2 H.sub.5 CH.sub.3 CHOCH.sub.3 a(80) oil both 6.81 s(20) 6.88/7.43 24 i-C.sub.3 H.sub.7 CH.sub.3 CHOCH.sub.3 a oil both 6.80 25 t-C.sub.4 H.sub.9 CH.sub.3 CHOCH.sub.3 a(80) oil 6.76/6.84 s(20) oil 6.85/7.46 26 H.sub.2 CCHCH.sub.2 CH.sub.3 CHOCH.sub.3 a oil both 6.81 s oil 6.90/7.46 27 H.sub.2 CCClCH.sub.2 CH.sub.3 CHOCH.sub.3 a oil 6.75/6.87 s oil 6.92/7.47 28 CH.sub.3 CClCHCH.sub.2 CH.sub.3 CHOCH.sub.3 29 HCCCH.sub.2 CH.sub.3 CHOCH.sub.3 30 Cyclopropyl CH.sub.3 CHOCH.sub.3 31 C.sub.6 H.sub.5 CH.sub.3 CHOCH.sub.3 32 4-Pyridyl CH.sub.3 CHOCH.sub.3 33 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 CHOCH.sub.3 a(90) 130-132 s(10) 34 2-Pyridylmethyl CH.sub.3 CHOCH.sub.3 35 5-Chlorthien-2- CH.sub.3 CHOCH.sub.3 ylmethyl 36 CH.sub.3 CO CH.sub.3 CHOCH.sub.3 37 C.sub.6 H.sub.5 CO CH.sub.3 CHOCH.sub.3 38 2-Furyl-CO CH.sub.3 CHOCH.sub.3 39 CH.sub.3 OOCCH.sub.2 CH.sub.3 CHOCH.sub.3 40 NCCH.sub.2 CH.sub.3 CHOCH.sub.3 41 H C.sub.6 H.sub.5 CHOCH.sub.3 42 CH.sub.3 C.sub.6 H.sub.5 CHOCH.sub.3 43 C.sub.6 H.sub.5 CH.sub.2 C.sub.6 H.sub.5 CHOCH.sub.3 44 H.sub.2 CCClCH.sub.2 C.sub.6 H.sub.5 CHOCH.sub.3 45 NCCH.sub.2 C.sub.6 H.sub. 5 CHOCH.sub.3 46 H p-CH.sub.3 OC.sub.6 H.sub.4 CHOCH.sub.3 47 CH.sub.3 p-CH.sub.3 OC.sub.6 H.sub.4 CHOCH.sub.3 48 C.sub.6 H.sub.5 CH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHOCH.sub.3 49 H.sub.2 CCClCH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHOCH.sub.3 50 NCCH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHOCH.sub.3 51 H H NOCH.sub.3 a oil 6.58/6.82 52 CH.sub.3 H NOCH.sub.3 a 86-88 53 C.sub.2 H.sub.5 H NOCH.sub.3 54 i-C.sub.3 H.sub.7 H NOCH.sub.3 55 t-C.sub.4 H.sub.9 H NOCH.sub.3 56 H.sub.2 CCHCH.sub.2 H NOCH.sub.3 57 H.sub.2 CCClCH.sub.2 H NOCH.sub.3 oil 6.60/6.82 oil 6.65/6.80 58 CH.sub.3CClCHCH.sub.2 H NOCH.sub.3 59 HCCCH.sub.2 H NOCH.sub.3 60 Cyclopropyl H NOCH.sub.3 61 C.sub.6 H.sub. 5 H NOCH.sub.3 62 4-Pyridyl H NOCH.sub.3 63 C.sub.6 H.sub.5 CH.sub.2 H NOCH.sub.3 a(85) 81-83 s(15) 64 2-Pyridylmethyl H NOCH.sub.3 65 5-Chlorothien- H NOCH.sub.3 2-ylmethyl 66 CH.sub.3 CO H NOCH.sub.3 67 C.sub.6 H.sub.5 CO H NOCH.sub.3 68 2-Furyl-CO H NOCH.sub.3 69 CH.sub.3 OOCCH.sub.2 H NOCH.sub.3 70 NCCH.sub.2 H NOCH.sub.3 71 H CH.sub.3 NOCH.sub.3 a 136-138 s 127-130 72 CH.sub.3 CH.sub.3 NOCH.sub.3 s 80-81 6.68/7.46 a oil 73 C.sub.2 H.sub.5 CH.sub.3 NOCH.sub.3 a(85) oil 6.60/6.82 s(15) 6.69/7.46 74 i-C.sub.3 H.sub.7 CH.sub.3 NOCH.sub.3 a oil 6.58/6.84 75 t-C.sub.4 H.sub.9 CH.sub.3 NOCH.sub.3 76 H.sub.2 CCHCH.sub.2 CH.sub.3 NOCH.sub.3 77 H.sub.2 CCClCH.sub.2 CH.sub.3 NOCH.sub.3 a oil 6.64/6.82 s oil 6.72/7.51 78 CH.sub.3 CClCHCH.sub.2 CH.sub.3 NOCH.sub.3 a oil 6.61/6.81 79 HCCCH.sub.2 CH.sub.3 NOCH.sub.3 80 Cyclopropyl CH.sub.3 NOCH.sub.3 81 C.sub.6 H.sub.5 CH.sub.3 NCCH.sub.3 82 4-Pyridyl CH.sub.3 NOCH.sub.3 83 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 NOCH.sub.3 a oil 6.62/6.82 84 2-Pyridylmethyl CH.sub.3 NOCH.sub.3 85 5-Chlorothien- CH.sub.3 NOCH.sub.3 a oil 6.63/6.81 2-ylmethyl 86 CH.sub.3 CO CH.sub.3 NOCH.sub.3 87 C.sub.6 H.sub.5 CO CH.sub.3 NOCH.sub.3 88 2-Furyl-CO CH.sub.3 NOCH.sub.3 89 CH.sub.3 OOCCH.sub.2 CH.sub.3 NOCH.sub.3 a oil 6.65/6.80 90 NCCH.sub.2 CH.sub.3 NOCH.sub.3 a 81-85 91 H C.sub.6 H.sub.5 NOCH.sub.3 a(70) 164-165 s(30) 92 CH.sub.3 C.sub.6 H.sub.5 NOCH.sub.3 a 175-179 93 C.sub.6 H.sub.5 CH.sub.2 C.sub.6 H.sub.5 NOCH.sub.3 94 H.sub.2 CCClCH.sub.2 C.sub.6 H.sub.5 NOCH.sub.3 95 NCCH.sub.2 C.sub.6 H.sub.5 NOCH.sub.3 96 H p-CH.sub.3 OC.sub.6 H.sub.4 NOCH.sub.3 97 CH.sub.3 p-CH.sub.3 OC.sub.6 H.sub.4 NOCH.sub.3 a(40) 100-104 s(60) 98 C.sub.6 H.sub.5 CH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 NOCH.sub.3 99 H.sub.2 CCClCH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 NOCH.sub.3100 NCCH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 NOCH.sub.3101 H H CHCH.sub.3102 CH.sub.3 H CHCH.sub.3103 C.sub.2 H.sub.5 H CHCH.sub.3104 i-C.sub.3 H.sub.7 H CHCH.sub.3105 t-C.sub.4 H.sub.9 H CHCH.sub.3106 H.sub.2 CCHCH.sub.2 H CHCH.sub.3107 H.sub.2 CCClCH.sub.2 H CHCH.sub.3108 CH.sub.3CClCHCH.sub.2 H CHCH.sub.3109 HCCCH.sub.2 H CHCH.sub.3110 Cyclopropyl H CHCH.sub.3111 C.sub.6 H.sub.5 H CHCH.sub.3112 4-Pyridyl H CHCH.sub.3113 C.sub.6 H.sub.5 CH.sub.2 H CHCH.sub.3114 2-Pyridylmethyl H CHCH.sub.3115 5-Chlorothien- H CHCH.sub.3 2-ylmethyl116 CH.sub.3 CO H CHCH.sub.3117 C.sub.6 H.sub.5 CO H CHCH.sub.3118 2-Furyl-CO H CHCH.sub.3119 CH.sub.3 OOCCH.sub.2 H CHCH.sub.3120 NCCH.sub.2 H CHCH.sub.3121 H CH.sub.3 CHCH.sub.3122 CH.sub.3 CH.sub.3 CHCH.sub.3123 C.sub.2 H.sub.5 CH.sub.3 CHCH.sub.3124 i-C.sub.3 H.sub.7 CH.sub.3 CHCH.sub.3125 t-C.sub.4 H.sub.9 CH.sub.3 CHCH.sub.3126 H.sub.2 CCHCH.sub.2 CH.sub.3 CHCH.sub.3127 H.sub.2 CCClCH.sub.2 CH.sub.3 CHCH.sub.3128 CH.sub.3 CClCHCH.sub.2 CH.sub.3 CHCH.sub.3129 HCCCH.sub.2 CH.sub.3 CHCH.sub.3130 Cyclopropyl CH.sub.3 CHCH.sub.3131 C.sub.6 H.sub.5 CH.sub.3 CHCH.sub.3132 4-Pyridyl CH.sub.3 CHCH.sub.3133 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 CHCH.sub.3134 2-Pyridylmethyl CH.sub.3 CHCH.sub.3135 5-Chlorothien- CH.sub.3 CHCH.sub.3 2-ylmethyl136 CH.sub.3 CO CH.sub.3 CHCH.sub.3137 C.sub.6 H.sub.5 CO CH.sub.3 CHCH.sub.3138 2-Furyl-CO CH.sub.3 CHCH.sub.3139 CH.sub.3 OOCCH.sub.2 CH.sub.3 CHCH.sub.3140 NCCH.sub.2 CH.sub.3 CHCH.sub.3141 H C.sub.6 H.sub.5 CHCH.sub.3142 CH.sub.3 C.sub.6 H.sub.5 CHCH.sub.3143 C.sub.6 H.sub.5 CH.sub.2 C.sub.6 H.sub.5 CHCH.sub.3144 H.sub.2 CCClCH.sub.2 C.sub.6 H.sub.5 CHCH.sub.3145 NCCH.sub.2 C.sub.6 H.sub.5 CHCH.sub.3146 H p-CH.sub.3 OC.sub.6 H.sub.4 CHCH.sub.3147 CH.sub.3 p-CH.sub.3 OC.sub.6 H.sub.4 CHCH.sub.3148 C.sub.6 H.sub.5 CH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHCH.sub.3149 H.sub.2 CCClCH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHCH.sub.3150 NCCH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHCH.sub.3151 H H CHC.sub.2 H.sub. 5152 CH.sub.3 H CHC.sub.2 H.sub.5153 C.sub.2 H.sub.5 H CHC.sub.2 H.sub.5154 i-C.sub.3 H.sub.7 H CHC.sub.2 H.sub.5155 t-C.sub.4 H.sub.9 H CHC.sub.2 H.sub.5156 H.sub.2 CCHCH.sub.2 H CHC.sub.2 H.sub.5157 H.sub.2 CCClCH.sub.2 H CHC.sub.2 H.sub.5158 CH.sub.3CClCHCH.sub.2 H CHC.sub.2 H.sub.5159 HCCCH.sub.2 H CHC.sub.2 H.sub.5160 Cyclopropyl H CHC.sub.2 H.sub.5161 C.sub.6 H.sub.5 H CHC.sub.2 H.sub.5162 4-Pyridyl H CHC.sub.2 H.sub.5163 C.sub.6 H.sub.5 CH.sub.2 H CHC.sub.2 H.sub.5164 2-Pyridylmethyl H CHC.sub.2 H.sub.5165 5-Chlorothien- H CHC.sub.2 H.sub.5 2-ylmethyl166 CH.sub.3 CO H CHC.sub.2 H.sub.5167 C.sub.6 H.sub.5 CO H CHC.sub.2 H.sub.5168 2-Furyl-CO H CHC.sub.2 H.sub.5169 CH.sub.3 OOCCH.sub.2 H CHC.sub.2 H.sub.5170 NCCH.sub.2 H CHC.sub.2 H.sub.5171 H CH.sub.3 CHC.sub.2 H.sub.5172 CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5173 C.sub.2 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5174 i-C.sub.3 H.sub.7 CH.sub.3 CHC.sub.2 H.sub.5175 t-C.sub.4 H.sub.9 CH.sub.3 CHC.sub.2 H.sub.5176 H.sub.2 CCHCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5177 H.sub.2 CCClCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5178 CH.sub.3 CClCHCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5179 HCCCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5180 Cyclopropyl CH.sub.3 CHC.sub.2 H.sub.5181 C.sub.6 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5182 4-Pyridyl CH.sub.3 CHC.sub.2 H.sub.5183 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5184 2-Pyridylmethyl CH.sub.3 CHC.sub.2 H.sub.5185 5-Chlorothien- CH.sub.3 CHC.sub.2 H.sub.5 2-ylmethyl186 CH.sub.3 CO CH.sub.3 CHC.sub.2 H.sub.5187 C.sub.6 H.sub.5 CO CH.sub.3 CHC.sub.2 H.sub.5188 2-FurylCO CH.sub.3 CHC.sub.2 H.sub.5189 CH.sub.3 OOCCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5190 NCCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5191 H C.sub.6 H.sub.5 CHC.sub.2 H.sub.5192 CH.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5193 C.sub.6 H.sub.5 CH.sub.2 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5194 H.sub.2 CCClCH.sub.2 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5195 NCCH.sub.2 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5196 H p-CH.sub.3 OC.sub.6 H.sub.4 CHC.sub.2 H.sub.5197 CH.sub.3 p-CH.sub.3 OC.sub.6 H.sub.4 CHC.sub.2 H.sub.5198 C.sub.6 H.sub.5 CH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHC.sub.2 H.sub.5199 H.sub.2 CCClCH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHC.sub.2 H.sub.5200 NCCH.sub.2 p-CH.sub.3 OC.sub.6 H.sub.4 CHC.sub.2 H.sub.5201 n-C.sub.4 H.sub.9 CH.sub.3 CHOCH.sub.3 a(90) oil both 6.80 s(10) 6.84/7.43202 2-Methylallyl CH.sub.3 CHOCH.sub.3 a(80) oil both 6.81 s(20) 6.92/7.50203 2-Bromoallyl CH.sub.3 CHOCH.sub.3 a(75) oil 6.75/6.87 s(25) 6.92/7.47204 2-Isopropyl- CH.sub.3 CHOCH.sub.3 a(70) 164-166 6-hydroxy-pyri- s(30) midin-4-yl205 CH.sub.3 t-C.sub.4 H.sub.9 CHOCH.sub.3206 C.sub.2 H.sub.5 t-C.sub.4 H.sub.9 CHOCH.sub.3207 i-C.sub.3 H.sub.7 t-C.sub.4 H.sub.9 CHOCH.sub.3208 t-C.sub.4 H.sub.9 t-C.sub.4 H.sub.9 CHOCH.sub.3209 2-Chloroallyl t-C.sub.4 H.sub.9 CHOCH.sub.3210 Benzyl t-C.sub.4 H.sub.9 CHOCH.sub.3211 CH.sub.3 CH.sub.3 O CHOCH.sub.3212 t-C.sub.4 H.sub.9 CH.sub.3 O CHOCH.sub.3213 2-Chloroallyl CH.sub.3 O CHOCH.sub.3214 Benzyl CH.sub.3 O CHOCH.sub.3215 n-C.sub.4 H.sub.9 CH.sub.3 NOCH.sub.3216 2-Methylallyl CH.sub.3 NOCH.sub.3 a(80) oil 6.62/6.83 s(20) 6.70/7.50217 2-Bromoallyl CH.sub.3 NOCH.sub.3 a(85) oil 6.64/6.80 s(15) 6.78/7.51218 2-Isopropyl- CH.sub.3 NOCH.sub.3 a(70) 176-178 6-hydroxy-pyri- s(30) midin-4-yl219 CH.sub.3 t-C.sub.4 H.sub.9 NOCH.sub.3 s 84-86220 C.sub.2 H.sub.5 t-C.sub.4 H.sub.9 NOCH.sub. 3221 i-C.sub.3 H.sub.7 t-C.sub.4 H.sub.9 NOCH.sub.3 s 6.59/7.40222 t-C.sub.4 H.sub.9 t-C.sub.4 H.sub.9 NOCH.sub.3 s oil 6.60/7.49223 2-Chloroallyl t-C.sub.4 H.sub.9 NOCH.sub.3 s oil 6.60/7.22224 Benzyl t-C.sub.4 H.sub.9 NOCH.sub.3225 CH.sub.3 CH.sub.3 O NOCH.sub.3226 t-C.sub.4 H.sub.9 CH.sub.3 O NOCH.sub.3227 2-Chloroallyl CH.sub.3 O NOCH.sub.3228 Benzyl CH.sub.3 O NOCH.sub.3__________________________________________________________________________ TABLE VII__________________________________________________________________________ ##STR17## Iso- m.p.No. Q.sub.m A X mer (.degree.C.) .delta. (CC .sub.--H)__________________________________________________________________________1 3-F H CHOCH.sub.32 2,6-F.sub.2 H CHOCH.sub.33 2-Cl H CHOCH.sub.34 3-Cl H CHOCH.sub.35 4-Cl H CHOCH.sub.36 2,6-Cl.sub.2 H CHOCH.sub.37 3,4-Cl.sub.2 H CHOCH.sub.38 3-Br H CHOCH.sub.39 4-I H CHOCH.sub.310 2-Cl, 6-F H CHOCH.sub.311 2-CH.sub.3 H CHOCH.sub.312 3-CH.sub.3 H CHOCH.sub.313 4-CH.sub.3 H CHOCH.sub.314 2,4-(CH.sub.3).sub.2 H CHOCH.sub.315 4,6-(CH.sub.3).sub.3 H CHOCH.sub.316 3-C.sub.2 H.sub.5 H CHOCH.sub.317 4-t-C.sub.4 H.sub.9 H CHOCH.sub.318 4-Cyclohexyl H CHOCH.sub.319 3-CH.sub.2 C.sub.6 H.sub.5 H CHOCH.sub.320 2-OCH.sub.3 H CHOCH.sub.321 3-OCH.sub.3 H CHOCH.sub.322 4-OCH.sub.3 H CHOCH.sub.323 2-O-i-C3H7 H CHOCH.sub.324 3-OCH.sub.2 C.sub.6 H.sub.5 H CHOCH.sub.325 3-CF.sub.3 H CHOCH.sub.326 3-NO.sub.2 H CHOCH.sub.327 4-NO.sub.2 H CHOCH.sub.328 3-Cyano H CHOCH.sub.329 2-Cl, 4-CH.sub.3 H CHOCH.sub.330 2-COOCH.sub.3 H CHOCH.sub.331 4-CH.sub.2 OCH.sub.3 H CHOCH.sub.332 4-COCH.sub.3 H CHOCH.sub.333 2-CH.sub.3 -4-COCH.sub.3 H CHOCH.sub.334 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHOCH.sub.335 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 H CHOCH.sub.3 CHCH.sub.236 3-F CH.sub.3 CHOCH.sub.3 a oil 6.77/6.8337 2,6-F.sub.2 CH.sub.3 CHOCH.sub.3 a 116-118 s 180-8238 2-Cl CH.sub.3 CHOCH.sub.339 3-Cl CH.sub.3 CHOCH.sub.340 4-Cl CH.sub.3 CHOCH.sub.341 2,6-Cl.sub.2 CH.sub.3 CHOCH.sub.3 a 131-133 s oil 6.85/7.3842 3,4-Cl.sub.2 CH.sub.3 CHOCH.sub.3 a oil 6.74/6.8743 3-Br CH.sub.3 CHOCH.sub.3 a oil 6.75/6.8544 4-I CH.sub.3 CHOCH.sub.345 2-Cl, 6-F CH.sub.3 CHOCH.sub.346 2-CH.sub.3 CH.sub.3 CHOCH.sub.3 a oil both 6.8247 3-CH.sub.3 CH.sub.3 CHOCH.sub.3 a(75) oil both 6.81 s(25) 6.89/7.4848 4-CH.sub.3 CH.sub.3 CHOCH.sub.3 a oil both 6.7849 2,4-(CH.sub.3).sub.2 CH.sub.3 CHOCH.sub.350 2,4,6-(CH.sub.3).sub.3 CH.sub.3 CHOCH.sub.351 3-C.sub.2 H.sub.5 CH.sub.3 CHOCH.sub.352 4-t-C.sub.4 H.sub.9 CH.sub.3 CHOCH.sub.353 4-Cyclohexyl CH.sub.3 CHOCH.sub.354 3-CH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHOCH.sub.355 2-OCH.sub.3 CH.sub.3 CHOCH.sub.356 3-OCH.sub.3 CH.sub.3 CHOCH.sub.357 4-OCH.sub.3 CH.sub.3 CHOCH.sub.358 2-O-i-C.sub.3 H.sub.7 CH.sub.3 CHOCH.sub.359 3-OCH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHOCH.sub.360 2-CF.sub.3 CH.sub.3 CHOCH.sub.3 a oil 6.76/6.8661 3-NO.sub.2 CH.sub.3 CHOCH.sub.362 4-NO.sub.2 CH.sub.3 CHOCH.sub.363 3-Cyano CH.sub.3 CHOCH.sub.3 a oil 6.73/6.8464 2-Cl, 4-CH.sub.3 CH.sub.3 CHOCH.sub.365 2-COOCH.sub.3 CH.sub.3 CHOCH.sub. 366 4-CH.sub.2 OCH.sub.3 CH.sub.3 CHOCH.sub.367 4-COCH.sub.3 CH.sub.3 CHOCH.sub.368 2-CH.sub.3 -4-OCH.sub.3 CH.sub.3 CHOCH.sub.369 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHOCH.sub.370 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CH.sub.3 CHOCH.sub.3 CHCH.sub.271 3-F H NOCH.sub.3 a 83-8572 2,6-F.sub.2 H NOCH.sub.3 a 120-12273 2-Cl H NOCH.sub.374 3-Cl H NOCH.sub.375 4-Cl H NOCH.sub.376 2,6-Cl.sub.2 H NOCH.sub.3 a(80) 127-129 s(20)77 3,4-Cl.sub.2 H NOCH.sub.3 a oil 6.57/6.7878 3-Br H NOCH.sub.3 a 126-12879 4-I H NOCH.sub.380 2-Cl, 6-F H NOCH.sub.381 2-CH.sub.3 H NOCH.sub.382 3-CH.sub.3 H NOCH.sub.383 4-CH.sub.3 H NOCH.sub.3 a oil 6.62/6.8284 2,4-(CH.sub.3).sub.2 H NOCH.sub.385 2,4,6-(CH.sub.3).sub.3 H NOCH.sub.386 3-C.sub.2 H.sub.5 H NOCH.sub.387 4-t-C.sub.4 H.sub.9 H NOCH.sub.388 4-Cyclohexyl H NOCH.sub.389 3-CH.sub.2 C.sub.6 H.sub.5 H NOCH.sub.390 2-OCH.sub.3 H NOCH.sub. 391 3-OCH.sub.3 H NOCH.sub.392 4-OCH.sub.3 H NOCH.sub.393 2-O-i-C.sub.3 H.sub.7 H NOCH.sub.394 3-OCH.sub.2 C.sub.6 H.sub.5 H NOCH.sub.395 3-CF.sub.3 H NOCH.sub.3 a(80) 63-66 s(20)96 3-NO.sub.2 H NOCH.sub.397 4-NO.sub.2 H NOCH.sub.398 3-Cyano H NOCH.sub.3 a oil 6.58/6.7899 2-Cl, 4-CH.sub.3 H NOCH.sub.3100 2-COOCH.sub.3 H NOCH.sub.3101 4-CH.sub.2 OCH.sub.3 H NOCH.sub.3102 4-COCH.sub.3 H NOCH.sub.3103 2-CH.sub.3 -4-COCH.sub.3 H NOCH.sub.3104 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H NOCH.sub.3105 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.3 H NOCH.sub.3 CHCH.sub.2106 3-F CH.sub.3 NOCH.sub.3 a oil 6.62/6.80107 2,6-F.sub.2 CH.sub.3 NOCH.sub.3 a 82-83 (Zers.)108 2-Cl CH.sub.3 NOCH.sub.3109 3-Cl CH.sub.3 NOCH.sub.3110 4-Cl CH.sub.3 NOCH.sub.3111 2,6-Cl.sub.2 CH.sub.3 NOCH.sub.3 a 126-128112 3,4-Cl.sub.2 CH.sub.3 NOCH.sub.3 a oil 6.62/6.78113 3-Br CH.sub.3 NOCH.sub.3 a oil 6.63/6.82114 4-I CH.sub.3 NOCH.sub.3115 2-Cl, 6-F CH.sub.3 NOCH.sub.3116 2-CH.sub.3 CH.sub.3 NOCH.sub.3 a oil 6.62/6.83117 3-CH.sub.3 CH.sub.3 NOCH.sub.3 a(80) oil 6.60/6.82 s(20) 6.75/7.49118 4-CH.sub.3 CH.sub.3 NOCH.sub.3119 2,4-(CH.sub.3).sub.2 CH.sub.3 NOCH.sub.3120 2,4,6-(CH.sub.3).sub.3 CH.sub.3 NOCH.sub.3121 3-C.sub.2 H.sub.5 CH.sub.3 NOCH.sub.3122 4-t-C.sub.4 H.sub.9 CH.sub.3 NOCH.sub.3123 4-Cyclohexyl CH.sub.3 NOCH.sub.3124 3-CH.sub.2 C.sub.6 H.sub.5 CH.sub.3 NOCH.sub.3125 2-OCH.sub.3 CH.sub.3 NOCH.sub.3126 3-OCH.sub.3 CH.sub.3 NOCH.sub.3127 4-OCH.sub.3 CH.sub.3 NOCH.sub.3128 2-O-i-C.sub.3 H.sub.7 CH.sub.3 NOCH.sub.3129 OCH.sub.2 C.sub.6 H.sub.5 CH.sub.3 NOCH.sub.3130 3-CF.sub.3 CH.sub.3 NOCH.sub.3 a oil 6.64/6.79131 3-NO.sub.2 CH.sub.3 NOCH.sub.3132 4-NO.sub.2 CH.sub.3 NOCH.sub.3 oil 6.65/6.79133 3-Cyano CH.sub.3 NOCH.sub.3 oil 6.64/6.79134 2-Cl, 4-CH.sub.3 CH.sub.3 NOCH.sub.3135 2-COOCH.sub.3 CH.sub.3 NOCH.sub.3136 4-CH.sub.2 OCH.sub.3 CH.sub.3 NOCH.sub.3137 4-COCH.sub.3 CH.sub.3 NOCH.sub.3138 2-CH.sub. 3 -4-COCH.sub.3 CH.sub.3 NOCH.sub.3139 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 NOCH.sub.3140 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CH.sub.3 NOCH.sub.3 CHCH.sub.2141 3-F H CHCH.sub.3142 2,6-F.sub.2 H CHCH.sub.3143 2-Cl H CHCH.sub.3144 3-Cl H CHCH.sub.3145 4-Cl H CHCH.sub.3146 2,6-Cl.sub.2 H CHCH.sub.3147 3,4-Cl.sub.2 H CHCH.sub.3148 3-Br H CHCH.sub.3149 4-I H CHCH.sub.3150 2-Cl, 6-F H CHCH.sub.3151 2-CH.sub.3 H CHCH.sub.3152 3-CH.sub.3 H CHCH.sub.3153 4-CH.sub.3 H CHCH.sub.3154 2,4-(CH.sub.3).sub. H CHCH.sub.3155 2,4,6-(CH.sub.3).sub.3 H CHCH.sub.3156 3-C.sub.2 H.sub.5 H CHCH.sub.3157 4-t-C.sub.4 H.sub.9 H CHCH.sub.3158 4-Cyclohexyl H CHCH.sub.3159 3-CH.sub.2 C.sub.6 H.sub.5 H CHCH.sub.3160 2-OCH.sub.3 H CHCH.sub.3161 3-OCH.sub.3 H CHCH.sub.3162 4-OCH.sub.3 H CHCH.sub.3163 2-O-i-C.sub.3 H.sub.7 H CHCH.sub.3164 3-OCH.sub.2 C.sub.6 H.sub.5 H CHCH.sub.3165 3-CF.sub.3 H CHCH.sub.3166 3-NO.sub.2 H CHCH.sub.3167 4-NO.sub.2 H CHCH.sub.3168 3-Cyano H CHCH.sub.3169 2-Cl, 4-CH.sub.3 H CHCH.sub.3170 2-COOCH.sub.3 H CHCH.sub.3171 4-CH.sub.2 CCH.sub.3 H CHCH.sub.3172 4-COCH.sub.3 H CHCH.sub.3173 2-CH.sub.3 -4-COCH.sub.3 H CHCH.sub.3174 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHCH.sub.3175 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 H CHCH.sub.3 CHCH.sub.2176 3-F CH.sub.3 CHCH.sub.3177 2,6-F.sub.2 CH.sub.3 CHCH.sub.3178 2-Cl CH.sub.3 CHCH.sub.3179 3-Cl CH.sub.3 CHCH.sub.3180 4-Cl CH.sub.3 CHCH.sub.3181 2,6-Cl.sub.2 CH.sub.3 CHCH.sub.3182 3,4-Cl.sub.2 CH.sub.3 CHCH.sub.3183 3-Br CH.sub.3 CHCH.sub.3184 4-I CH.sub.3 CHCH.sub.3185 2-Cl, 6-F CH.sub.3 CHCH.sub.3186 2-CH.sub.3 CH.sub.3 CHCH.sub.3187 3-CH.sub.3 CH.sub.3 CHCH.sub.3188 4-CH.sub.3 CH.sub.3 CHCH.sub.3189 2,4-(CH.sub.3).sub.2 CH.sub.3 CHCH.sub.3190 2,4,6-(CH.sub.3).sub.3 CH.sub.3 CHCH.sub.3191 3-C.sub.2 H.sub.5 CH.sub.3 CHCH.sub.3192 4-t-C.sub.4 H.sub.9 CH.sub.3 CHCH.sub.3193 4-Cyclohexyl CH.sub.3 CHCH.sub.3194 3-CH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHCH.sub.3195 2-OCH.sub.3 CH.sub.3 CHCH.sub.3196 3-OCH.sub.3 CH.sub.3 CHCH.sub.3197 4-OCH.sub.3 CH.sub.3 CHCH.sub.3198 2-O-i-C.sub.3 H.sub.7 CH.sub.3 CHCH.sub.3199 3-OCH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHCH.sub.3200 3-CF.sub.3 CH.sub.3 CHCH.sub.3201 3-NO.sub.2 CH.sub.3 CHCH.sub.3202 4-NO.sub.2 CH.sub.3 CHCH.sub.3203 3-Cyano CH.sub.3 CHCH.sub.3204 2-Cl, 4-CH.sub.3 CH.sub.3 CHCH.sub.3205 2-COOCH.sub.3 CH.sub.3 CHCH.sub.3206 4-CH.sub.2 OCH.sub.3 CH.sub.3 CHCH.sub.3207 4-COCH.sub.3 CH.sub.3 CHCH.sub.3208 2-CH.sub.3 -4-COCH.sub.3 CH.sub.3 CHCH.sub.3209 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHCH.sub.3210 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CH.sub.3 CHCH.sub.3 CHCH.sub.2211 3-F H CHC.sub.2 H.sub.5212 2,6-F.sub.2 H CHC.sub.2 H.sub.5213 2-Cl H CHC.sub.2 H.sub.5214 3-Cl H CHC.sub.2 H.sub.5215 4-Cl H CHC.sub.2 H.sub.5216 2,6-Cl.sub.2 H CHC.sub.2 H.sub.5217 3,4-Cl.sub.2 H CHC.sub.2 H.sub.5218 3-Br H CHC.sub.2 H.sub.5219 4-I H CHC.sub.2 H.sub.5220 2-Cl, 6-F H CHC.sub.2 H.sub.5221 2-CH.sub.3 H CHC.sub.2 H.sub.5222 3-CH.sub.3 H CHC.sub.2 H.sub.5223 4-CH.sub.3 H CHC.sub.2 H.sub.5224 2,4-(CH.sub.3).sub.2 H CHC.sub.2 H.sub.5225 2,4,6-(CH.sub.3).sub.3 H CHC.sub.2 H.sub.5226 3-C.sub.2 H.sub.5 H CHC.sub.2 H.sub.5227 4-t-C.sub.4 H.sub.9 H CHC.sub.2 H.sub.5228 4-Cyclohexyl H CHC.sub.2 H.sub.5229 3-CH.sub.2 C.sub.6 H.sub.5 H CHC.sub.2 H.sub.5230 2-OCH.sub.3 H CHC.sub.2 H.sub.5231 3-OCH.sub.3 H CHC.sub.2 H.sub.5232 4-OCH.sub.3 H CHC.sub.2 H.sub.5233 2-O-i-C.sub.3 H.sub.7 H CHC.sub.2 H.sub.5234 3-OCH.sub.2 C.sub.6 H.sub.5 H CHC.sub.2 H.sub.5235 3-CF.sub.3 H CHC.sub.2 H.sub.5236 3-NO.sub.2 H CHC.sub.2 H.sub.5237 4-NO.sub.2 H CHC.sub.2 H.sub.5238 3-Cyano H CHC.sub.2 H.sub.5239 2-Cl, 4-CH.sub.3 H CHC.sub.3 H.sub.5240 2-COOCH.sub.3 H CHC.sub.2 H.sub.5241 4-CH.sub.2 OCH.sub.3 H CHC.sub.2 H.sub.5242 4-COCH.sub.3 H CHC.sub.2 H.sub.5243 2-CH.sub.3 -4-COCH.sub.3 H CHC.sub.2 H.sub.5244 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 H CHC.sub.2 H.sub.5245 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 H CHC.sub.2 H.sub.5 CHCH.sub.2246 3-F CH.sub.3 CHC.sub.2 H.sub.5247 2,6-F.sub.2 CH.sub.3 CHC.sub.2 H.sub.5248 2-Cl CH.sub.3 CHC.sub.2 H.sub.5249 3-Cl CH.sub.3 CHC.sub.2 H.sub.5250 4-Cl CH.sub.3 CHC.sub.2 H.sub.5251 2,6-Cl.sub.2 CH.sub.3 CHC.sub.2 H.sub.5252 3,4-Cl.sub.2 CH.sub.3 CHC.sub.2 H.sub.5253 3-Br CH.sub.3 CHC.sub.2 H.sub.5254 4-I CH.sub.3 CHC.sub.2 H.sub.5255 2-Cl, 6-F CH.sub.3 CHC.sub.2 H.sub.5256 2-CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5257 3-CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5258 4-CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5259 2,4-(CH.sub.3).sub.2 CH.sub.3 CHC.sub.2 H.sub.5260 2,4,6-(CH.sub.3).sub.3 CH.sub.3 CHC.sub.2 H.sub.5261 3-C.sub.2 H.sub.5 CH.sub. 3 CHC.sub.2 H.sub.5262 4-t-C.sub.4 H.sub.9 CH.sub.3 CHC.sub.2 H.sub.5263 4-Cyclohexyl CH.sub.3 CHC.sub.2 H.sub.5264 3-CH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5265 2-OCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5266 3-OCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5267 4-OCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5268 2-O-i-C.sub.3 H.sub.7 CH.sub.3 CHC.sub.2 H.sub.5269 3-OCH.sub.2 C.sub.6 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5270 3-CF.sub.3 CH.sub.3 CHC.sub.2 H.sub.5271 3-NO.sub.2 CH.sub.3 CHC.sub.2 H.sub.5272 4-NO.sub.2 CH.sub.3 CHC.sub.2 H.sub.5273 3-Cyano CH.sub.3 CHC.sub.2 H.sub.5274 2-Cl, 4-CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5275 2-COOCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5276 4-CH.sub.2 OCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5277 4-COCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5278 2-CH.sub.3 -4-COCH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5279 4-C(CH.sub.3)NOCH.sub.2 CHCH.sub.2 CH.sub.3 CHC.sub.2 H.sub.5280 2-CH.sub.3 -4-C(CH.sub.3)NOCH.sub.2 CH.sub.3 CH CH.sub.2281 4-F CH.sub.3 CHOCH.sub.3 a oil 6.76/6.83282 2-OCH.sub.3 t-C.sub.4 H.sub.9 CHOCH.sub.3283 3-F t-C.sub.4 H.sub.9 CHOCH.sub.3284 4-CH.sub.3 t-C.sub.4 H.sub.9 CHOCH.sub.3285 3,5-Cl.sub.2 t-C.sub.4 H.sub.9 CHOCH.sub.3286 2-OCH.sub.3 CH.sub.3 O CHOCH.sub.3287 3-CF.sub.3 CH.sub.3 O CHOCH.sub.3288 4-CH.sub.3 CH.sub.3 O CHOCH.sub.3289 3,5-Cl.sub.2 CH.sub.3 O CHOCH.sub.3290 4-F CH.sub.3 NOCH.sub.3 a oil 6.62/6.80291 2-OCH.sub.3 t-C.sub.4 H.sub.9 NOCH.sub.3292 3-F t-C.sub.4 H.sub.9 NOCH.sub.3 s oil 6.4/7.44293 4-CH.sub.3 t-C.sub.4 H.sub.9 NOCH.sub.3294 3,5-Cl.sub.2 t-C.sub.4 H.sub.9 NOCH.sub.3295 2-OCH.sub.3 CH.sub.3 O NOCH.sub.3296 3-CF.sub.3 CH.sub.3 O NOCH.sub.3297 4-CH.sub.3 CH.sub.3 O NOCH.sub.3298 3,5-Cl.sub.2 CH.sub.3 O NOCH.sub.3__________________________________________________________________________ TABLE VIII__________________________________________________________________________ ##STR18## Iso- m.p.No. R R' A X mer (.degree.C.) .delta. (CC .sub.-- H)__________________________________________________________________________1 H H H CHOCH.sub.32 CH.sub.3 H H CHOCH.sub.33 t-C.sub.4 H.sub.9 H H CHOCH.sub.34 C.sub.6 H.sub.5 H H CHOCH.sub.35 2-ClC.sub.6 H.sub.4 H H CHOCH.sub.36 3-NO.sub.2 C.sub.6 H.sub.4 H H CHOCH.sub.37 4-CH.sub.3 OC.sub.6 H.sub.4 H H CHOCH.sub.38 C.sub.6 H.sub.5 CH.sub.2 H H CHOCH.sub.39 2-ClC.sub.6 H.sub.4 CH.sub.2 H H CHOCH.sub.310 3-NO.sub.2 C.sub.6 H.sub.4 CH.sub.2 H H CHOCH.sub.311 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 H H CHOCH.sub.312 CH.sub.3 CO H H CHOCH.sub.313 C.sub.6 H.sub.5 CO H H CHOCH.sub.314 CH.sub.3 CH.sub.3 H CHOCH.sub.315 C.sub.6 H.sub.5 CH.sub.3 H CHOCH.sub.316 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 H CHOCH.sub.317 CH.sub.3 CO CH.sub.3 H CHOCH.sub.318 C.sub.6 H.sub.5 CO CH.sub.3 H CHOCH.sub.319 H H CH.sub.3 CHOCH.sub.320 CH.sub.3 H CH.sub.3 CHOCH.sub.321 t-C.sub.4 H.sub.9 H CH.sub.3 CHOCH.sub.322 C.sub.6 H.sub.5 H CH.sub.3 CHOCH.sub.323 2-Cl-C.sub.6 H.sub.4 H CH.sub.3 CHOCH.sub.324 3-NO.sub.2C.sub.6 H.sub.4 H CH.sub.3 CHOCH.sub.325 4-CH.sub.3 OC.sub.6 H.sub.4 H CH.sub.3 CHOCH.sub.326 C.sub.6 H.sub.5 CH.sub.2 H CH.sub.3 CHOCH.sub.327 2-ClC.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHOCH.sub.328 3-NO.sub.2 C.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHOCH.sub.329 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHOCH.sub.330 CH.sub.3 CO H CH.sub.3 CHOCH.sub.331 C.sub.6 H.sub.5 CO H CH.sub.3 CHOCH.sub.332 CH.sub.3 CH.sub.3 CH.sub.3 CHOCH.sub.333 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 CHOCH.sub.334 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 CH.sub.3 CHOCH.sub.335 CH.sub.3 CO CH.sub.3 CH.sub.3 CHOCH.sub.336 C.sub.6 H.sub.5 CO CH.sub.3 CH.sub.3 CHOCH.sub.337 CH.sub.3 H C.sub.6 H.sub.5 CHOCH.sub.338 C.sub.6 H.sub.5 H C.sub.6 H.sub.5 CHOCH.sub.339 C.sub.6 H.sub.5 CH.sub.2 H C.sub.6 H.sub.5 CHOCH.sub.340 CH.sub.3 CO H C.sub.6 H.sub.5 CHOCH.sub.341 C.sub.6 H.sub.5 CO H C.sub.6 H.sub.5 CHOCH.sub.342 CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 CHOCH.sub.343 C.sub.6 H.sub.5 CH.sub.3 C.sub.6 H.sub.5 CHOCH.sub.344 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 C.sub.6 H.sub.5 CHOCH.sub.345 CH.sub.3 CO CH.sub.3 C.sub.6 H.sub.5 CHOCH.sub.346 C.sub.6 H.sub.5 CO CH.sub.3 C.sub.6 H.sub.5 CHOCH.sub.347 H H H NOCH.sub.348 CH.sub.3 H H NOCH.sub.349 t-C.sub.4 H.sub.9 H H NOCH.sub.350 C.sub.6 H.sub.5 H H NOCH.sub.351 2-ClC.sub.6 H.sub.4 H H NOCH.sub.352 3-NO.sub.2 C.sub.6 H.sub.4 H H NOCH.sub.353 4-CH.sub.3 OC.sub.6 H.sub.4 H H NOCH.sub.354 C.sub.6 H.sub.5 CH.sub.2 H H NOCH.sub.355 2-ClC.sub.6 H.sub.4 CH.sub.2 H H NOCH.sub.356 3-NO.sub.2 C.sub.6 H.sub.4 CH.sub.2 H H NOCH.sub.357 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 H H NOCH.sub.358 CH.sub.3 CO H H NOCH.sub.359 C.sub.6 H.sub.5 CO H H NOCH.sub.360 CH.sub.3 CH.sub.3 H NOCH.sub.361 C.sub.6 H.sub.5 CH.sub.3 H NOCH.sub.362 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 H NOCH.sub.363 CH.sub.3 CO CH.sub.3 H NOCH.sub.364 C.sub.6 H.sub.5 CO CH.sub.3 H NOCH.sub.365 H H CH.sub.3 NOCH.sub.366 CH.sub.3 H CH.sub.3 NOCH.sub.367 t-C.sub.4 H.sub.9 H CH.sub.3 NOCH.sub.368 C.sub.6 H.sub.5 H CH.sub.3 NOCH.sub.3 a 155-15869 2-Cl-C.sub.6 H.sub.4 H CH.sub.3 NOCH.sub.370 3-NO.sub.2C.sub.6 H.sub.4 H CH.sub.3 NOCH.sub.3 a 170 (de- comp.)71 4-CH.sub.3 OC.sub.6 H.sub.4 H CH.sub.3 NOCH.sub.372 C.sub.6 H.sub.5 CH.sub.2 H CH.sub.3 NOCH.sub.373 2-ClC.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 NOCH.sub.374 3-NO.sub.2 C.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 NOCH.sub.375 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 NOCH.sub.376 CH.sub.3 CO H CH.sub.3 NOCH.sub.377 C.sub.6 H.sub.5 CO H CH.sub.3 NOCH.sub.378 CH.sub.3 CH.sub.3 CH.sub.3 NOCH.sub.379 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 NOCH.sub.380 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 CH.sub.3 NOCH.sub.381 CH.sub.3 CO CH.sub.3 CH.sub.3 NOCH.sub.382 C.sub.6 H.sub.5 CO CH.sub.3 CH.sub.3 NOCH.sub.383 CH.sub.3 H C.sub.6 H.sub.5 NOCH.sub.3 s oil 6.57/7.5284 C.sub.6 H.sub.5 H C.sub.6 H.sub.5 NOCH.sub.385 C.sub.6 H.sub.5 CH.sub.2 H C.sub.6 H.sub.5 NOCH.sub.386 CH.sub.3 CO H C.sub.6 H.sub.5 NOCH.sub.387 C.sub.6 H.sub.5 CO H C.sub.6 H.sub.5 NOCH.sub.388 CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 NOCH.sub.389 C.sub.6 H.sub.5 CH.sub.3 C.sub.6 H.sub.5 NOCH.sub.390 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 C.sub.6 H.sub.5 NOCH.sub.391 CH.sub.3 CO CH.sub.3 C.sub.6 H.sub.5 NOCH.sub.392 C.sub.6 H.sub.5 CO CH.sub.3 C.sub.6 H.sub.5 NOCH.sub.393 H H H CHCH.sub.394 CH.sub.3 H H CHCH.sub.395 t-C.sub.4 H.sub.9 H H CHCH.sub.396 C.sub.6 H.sub.5 H H CHCH.sub.397 2-ClC.sub.6 H.sub.4 H H CHCH.sub.398 3-NO.sub.2 C.sub.6 H.sub.4 H H CHCH.sub.399 4-CH.sub.3 OC.sub.6 H.sub.4 H H CHCH.sub.3100 C.sub.6 H.sub.5 CH.sub. 2 H H CHCH.sub.3101 2-ClC.sub.6 H.sub.4 CH.sub.2 H H CHCH.sub.3102 3-NO.sub.2 C.sub.6 H.sub.4 CH.sub.2 H H CHCH.sub.3103 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 H H CHCH.sub.3104 CH.sub.3 CO H H CHCH.sub.3105 C.sub.6 H.sub.5 CO H H CHCH.sub.3106 CH.sub.3 CH.sub.3 H CHCH.sub.3107 C.sub.6 H.sub.5 CH.sub.3 H CHCH.sub.3108 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 H CHCH.sub.3109 CH.sub.3 CO CH.sub.3 H CHCH.sub.3110 C.sub.6 H.sub.5 CO CH.sub.3 H CHCH.sub.3111 H H CH.sub.3 CHCH.sub.3112 CH.sub.3 H CH.sub.3 CHCH.sub.3113 t-C.sub.4 H.sub.9 H CH.sub.3 CHCH.sub.3114 C.sub.6 H.sub.5 H CH.sub.3 CHCH.sub.3115 2-Cl-C.sub.6 H.sub.4 H CH.sub.3 CHCH.sub.3116 3-NO.sub.2C.sub.6 H.sub.4 H CH.sub.3 CHCH.sub.3117 4-CH.sub.3 OC.sub.6 H.sub.4 H CH.sub.3 CHCH.sub.3118 C.sub.6 H.sub.5 CH.sub.2 H CH.sub.3 CHCH.sub.3119 2-ClC.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHCH.sub.3120 3-NO.sub.2 C.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHCH.sub.3121 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHCH.sub.3122 CH.sub.3 CO H CH.sub.3 CHCH.sub.3123 C.sub.6 H.sub.5 CO H CH.sub.3 CHCH.sub.3124 CH.sub.3 CH.sub.3 CH.sub.3 CHCH.sub.3125 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 CHCH.sub.3126 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 CH.sub.3 CHCH.sub.3127 CH.sub.3 CO CH.sub.3 CH.sub.3 CHCH.sub.3128 C.sub.6 H.sub.5 CO CH.sub.3 CH.sub.3 CHCH.sub.3129 CH.sub.3 H C.sub.6 H.sub.5 CHCH.sub.3130 C.sub.6 H.sub.5 H C.sub.6 H.sub.5 CHCH.sub.3131 C.sub.6 H.sub.5 CH.sub.2 H C.sub.6 H.sub.5 CHCH.sub.3132 CH.sub.3 CO H C.sub.6 H.sub.5 CHCH.sub.3133 C.sub.6 H.sub.5 CO H C.sub.6 H.sub.5 CHCH.sub.3134 CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 CHCH.sub.3135 C.sub.6 H.sub.5 CH.sub.3 C.sub.6 H.sub.5 CHCH.sub.3136 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 C.sub.6 H.sub.5 CHCH.sub.3137 CH.sub.3 CO CH.sub.3 C.sub.6 H.sub.5 CHCH.sub.3138 C.sub.6 H.sub.5 CO CH.sub.3 C.sub.6 H.sub.5 CHCH.sub.3139 H H H CHC.sub.2 H.sub.5140 CH.sub.3 H H CHC.sub.2 H.sub.5141 t-C.sub.4 H.sub.9 H H CHC.sub.2 H.sub.5142 C.sub.6 H.sub.5 H H CHC.sub.2 H.sub.5143 2-ClC.sub.6 H.sub.4 H H CHC.sub.2 H.sub.5144 3-NO.sub.2 C.sub.6 H.sub.4 H H CHC.sub.2 H.sub.5145 4-CH.sub.3 OC.sub.6 H.sub.4 H H CHC.sub.2 H.sub.5146 C.sub.6 H.sub.5 CH.sub.2 H H CHC.sub.2 H.sub.5147 2-ClC.sub.6 H.sub.4 CH.sub.2 H H CHC.sub.2 H.sub.5148 3-NO.sub.2 C.sub.6 H.sub.4 CH.sub.2 H H CHC.sub.2 H.sub.5149 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 H H CHC.sub.2 H.sub.5150 CH.sub.3 CO H H CHC.sub.2 H.sub.5151 C.sub.6 H.sub.5 CO H H CHC.sub.2 H.sub.5152 CH.sub.3 CH.sub.3 H CHC.sub.2 H.sub.5153 C.sub.6 H.sub.5 CH.sub.3 H CHC.sub.2 H.sub.5154 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 H CHC.sub.2 H.sub.5155 CH.sub.3 CO CH.sub.3 H CHC.sub.2 H.sub.5156 C.sub.6 H.sub.5 CO CH.sub.3 H CHC.sub.2 H.sub.5157 H H CH.sub.3 CHC.sub.2 H.sub.5158 CH.sub.3 H CH.sub.3 CHC.sub.2 H.sub.5159 t-C.sub.4 H.sub.9 H CH.sub.3 CHC.sub.2 H.sub.5160 C.sub.6 H.sub.5 H CH.sub.3 CHC.sub.2 H.sub.5161 2-Cl-C.sub.6 H.sub.4 H CH.sub.3 CHC.sub.2 H.sub.5162 3-NO.sub.2C.sub.6 H.sub.4 H CH.sub.3 CHC.sub.2 H.sub.5163 4-CH.sub.3 OC.sub.6 H.sub.4 H CH.sub.3 CHC.sub.2 H.sub.5164 C.sub.6 H.sub.5 CH.sub.2 H CH.sub.3 CHC.sub.2 H.sub.5165 2-ClC.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHC.sub.2 H.sub.5166 3-NO.sub.2 C.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHC.sub.2 H.sub.5167 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 H CH.sub.3 CHC.sub.2 H.sub.5168 CH.sub.3 CO H CH.sub.3 CHC.sub.2 H.sub.5169 C.sub.6 H.sub.5 CO H CH.sub.3 CHC.sub.2 H.sub.5170 CH.sub.3 CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5171 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5172 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5173 CH.sub.3 CO CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5174 C.sub.6 H.sub.5 CO CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5175 CH.sub.3 H C.sub.6 H.sub.5 CHC.sub.2 H.sub.5176 C.sub.6 H.sub.5 H C.sub.6 H.sub.5 CHC.sub.2 H.sub.5177 C.sub.6 H.sub.5 CH.sub.2 H C.sub.6 H.sub.5 CHC.sub.2 H.sub.5178 CH.sub.3 CO H C.sub.6 H.sub.5 CHC.sub.2 H.sub.5179 C.sub.6 H.sub.5 CO H C.sub.6 H.sub.5 CHC.sub.2 H.sub.5180 CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5181 C.sub.6 H.sub.5 CH.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5182 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5183 CH.sub.3 CO CH.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5184 C.sub.6 H.sub.5 CO CH.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5__________________________________________________________________________ TABLE IX__________________________________________________________________________ ##STR19##No. A X m.p. (.degree.C.) .delta. (C .sub.--H.sub.2C .sub.--H.sub.2)__________________________________________________________________________1 H CHOCH.sub.32 CH.sub.3 CHOCH.sub.33 t-C.sub.4 H.sub.9 CHOCH.sub.34 C.sub.6 H.sub.5 CHOCH.sub.35 2-CH.sub.3 C.sub.6 H.sub.4 CHOCH.sub.36 2-ClC.sub.6 H.sub.4 CHOCH.sub.37 3-CH.sub.3 OC.sub.6 H.sub.4 CHOCH.sub.38 4-Cyano-C.sub.6 H.sub.4 CHOCH.sub.39 2,6-F.sub.2C.sub.6 H.sub.3 CHOCH.sub.310 .beta.-Naphthyl CHOCH.sub.311 3-Pyridyl CHOCH.sub.312 2-Furyl CHOCH.sub.313 N-Methyl-3-indolyl CHOCH.sub.314 CF.sub.3 CHOCH.sub.315 HO CHOCH.sub.316 t-C.sub.4 H.sub.9 O CHOCH.sub.317 CH.sub.2CHCH.sub.2 O CHOCH.sub.318 C.sub.6 H.sub.5 CH.sub.2 O CHOCH.sub.319 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.320 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.321 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.322 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.323 2,6-F.sub.2C.sub.6 H.sub.3 CH.sub.2 O CHOCH.sub.324 2-Pyridyl-methoxy CHOCH.sub.325 t-C.sub.4 H.sub.9(CH.sub.3).sub.2SiO CHOCH.sub.326 CH.sub.3 NH CHOCH.sub.327 C.sub.6 H.sub.5 NH CHOCH.sub.328 2-CH.sub.3 C.sub.6 H.sub.4 NH CHOCH.sub.329 2-ClC.sub.6 H.sub.4 NH CHOCH.sub.330 3-CH.sub.3 OC.sub.6 H.sub.4 NH CHOCH.sub.331 4-Cyano-C.sub.6 H.sub.4 NH CHOCH.sub.332 2,6-F.sub.2C.sub.6 H.sub.3 NH CHOCH.sub.333 C.sub.6 H.sub.5 NCH.sub.3 CHOCH.sub.334 2-ClC.sub.6 H.sub.4 NCH.sub.3 CHOCH.sub.335 4-Cyano-C.sub.6 H.sub.4 NCH.sub.3 CHOCH.sub.336 C.sub.6 H.sub.5 CH.sub.2 NH CHOCH.sub.337 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NH CHOCH.sub.338 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHOCH.sub.339 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NH CHOCH.sub.340 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NH CHOCH.sub.341 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 NH CHOCH.sub.342 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHOCH.sub.343 2-ClC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 CHOCH.sub.344 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 CHOCH.sub.345 HS CHOCH.sub.346 C.sub.6 H.sub.5 CH.sub.2 S CHOCH.sub.347 H NOCH.sub.348 CH.sub.3 NOCH.sub.3 oil 2.69 (mc)49 t-C.sub.4 H.sub.9 NOCH.sub.350 C.sub.6 H.sub.5 NOCH.sub.3 oil51 2-CH.sub.3 C.sub.6 H.sub.4 NOCH.sub.352 2-ClC.sub.6 H.sub.4 NOCH.sub.353 3-CH.sub.3 OC.sub.6 H.sub.4 NOCH.sub.354 4-Cyano-C.sub.6 H.sub.4 NOCH.sub.355 2,6-F.sub.2C.sub.6 H.sub.3 NOCH.sub.356 .beta.-Naphthyl NOCH.sub.357 3-Pyridyl NOCH.sub.358 2-Furyl NOCH.sub.359 N-Methyl-3-indolyl NOCH.sub.360 CF.sub.3 NOCH.sub.361 HO NOCH.sub.362 t-C.sub.4 H.sub.9 O NOCH.sub.363 CH.sub.2CHCH.sub.2 O NOCH.sub.364 C.sub.6 H.sub.5 CH.sub.2 O NOCH.sub.365 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.366 2-ClC.sub.6 H.sub. 4 CH.sub.2 O NOCH.sub.367 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.368 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.369 2,6-F.sub.2C.sub.6 H.sub.3 CH.sub.2 O NOCH.sub.370 2-Pyridyl-methoxy NOCH.sub.371 t-C.sub.4 H.sub.9(CH.sub.3).sub.2SiO NOCH.sub.372 CH.sub.3 NH NOCH.sub.373 C.sub.6 H.sub.5 NH NOCH.sub.374 2-CH.sub.3 C.sub.6 H.sub.4 NH NOCH.sub.375 2-ClC.sub.6 H.sub.4 NH NOCH.sub.376 3-CH.sub.3 OC.sub.6 H.sub.4 NH NOCH.sub.377 4-Cyano-C.sub.6 H.sub.4 NH NOCH.sub.378 2,6-F.sub.2C.sub.6 H.sub.3 NH NOCH.sub.379 C.sub.6 H.sub.5 NCH.sub.3 NOCH.sub.380 2-ClC.sub.6 H.sub.4 NCH.sub.3 NOCH.sub.381 4-Cyano-C.sub.6 H.sub.4 NCH.sub.3 NOCH.sub.382 C.sub.6 H.sub.5 CH.sub.2 NH NOCH.sub.383 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NH NOCH.sub.384 2-ClC.sub.6 H.sub.4 CH.sub.2 NH NOCH.sub.385 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NH NOCH.sub.386 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NH NOCH.sub.387 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 NH NOCH.sub.388 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 NOCH.sub.389 2-ClC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 NOCH.sub.390 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 NOCH.sub.391 HS NOCH.sub.392 C.sub.6 H.sub.5 CH.sub.2 S NOCH.sub.393 H CHCH.sub.394 CH.sub.3 CHCH.sub.395 t-C.sub.4 H.sub.9 CHCH.sub.396 C.sub.6 H.sub.5 CHCH.sub.397 2-CH.sub.3 C.sub.6 H.sub.4 CHCH.sub.398 2-ClC.sub.6 H.sub.4 CHCH.sub.399 3-CH.sub.3 OC.sub.6 H.sub.4 CHCH.sub.3100 4-Cyano-C.sub.6 H.sub.4 CHCH.sub.3101 2,6-F.sub.2C.sub.6 H.sub.3 CHCH.sub.3102 .beta.-Naphthyl CHCH.sub.3103 3-Pyridyl CHCH.sub.3104 2-Furyl CHCH.sub.3105 N-Methyl-3-indolyl CHCH.sub.3106 CF.sub.3 CHCH.sub.3107 HO CHCH.sub.3108 t-C.sub.4 H.sub.9 O CHCH.sub.3109 CH.sub.2CHCH.sub.2 O CHCH.sub.3110 C.sub.6 H.sub.5 CH.sub.2 O CHCH.sub.3111 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3112 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3113 3-CH.sub. 3 OC.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3114 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3115 2,6-F.sub.2C.sub.6 H.sub.3 CH.sub.2 O CHCH.sub.3116 2-Pyridyl-methoxy CHCH.sub.3117 t-C.sub.4 H.sub.9(CH.sub.3).sub.2SiO CHCH.sub.3118 CH.sub.3 NH CHCH.sub.3119 C.sub.6 H.sub.5 NH CHCH.sub.3120 2-CH.sub.3 C.sub.6 H.sub.4 NH CHCH.sub.3121 2-ClC.sub.6 H.sub.4 NH CHCH.sub.3122 3-CH.sub.3 OC.sub.6 H.sub.4 NH CHCH.sub.3123 4-Cyano-C.sub.6 H.sub.4 NH CHCH.sub.3124 2,6-F.sub.2C.sub.6 H.sub.3 NH CHCH.sub.3125 C.sub.6 H.sub.5 NCH.sub.3 CHCH.sub.3126 2-ClC.sub.6 H.sub.4 NCH.sub.3 CHCH.sub.3127 4-Cyano-C.sub.6 H.sub.4 NCH.sub.3 CHCH.sub.3128 C.sub.6 H.sub.5 CH.sub.2 NH CHCH.sub.3129 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NH CHCH.sub.3130 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHCH.sub.3131 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NH CHCH.sub.3132 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NH CHCH.sub.3133 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 NH CHCH.sub.3134 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHCH.sub.3135 2-ClC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 CHCH.sub.3136 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 CHCH.sub.3137 HS CHCH.sub.3138 C.sub.6 H.sub.5 CH.sub.2 S CHCH.sub.3139 H CHC.sub.2 H.sub.5140 CH.sub.3 CHC.sub.2 H.sub.5141 t-C.sub.4 H.sub.9 CHC.sub.2 H.sub.5142 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5143 2-CH.sub.3 C.sub.6 H.sub.4 CHC.sub.2 H.sub.5144 2-ClC.sub.6 H.sub.4 CHC.sub.2 H.sub.5145 3-CH.sub.3 OC.sub.6 H.sub.4 CHC.sub.2 H.sub.5146 4-Cyano-C.sub.6 H.sub.4 CHC.sub.2 H.sub.5147 2,6-F.sub.2C.sub.6 H.sub.3 CHC.sub.2 H.sub.5148 .beta.-Naphthyl CHC.sub.2 H.sub.5149 3-Pyridyl CHC.sub.2 H.sub.5150 2-Furyl CHC.sub.2 H.sub.5151 N-Methyl-3-indolyl CHC.sub.2 H.sub.5152 CF.sub.3 CHC.sub.2 H.sub.5153 HO CHC.sub.2 H.sub.5154 t-C.sub.4 H.sub.9 O CHC.sub.2 H.sub.5155 CH.sub.2CHCH.sub.2 O CHC.sub.2 H.sub.5156 C.sub.6 H.sub.5 CH.sub.2 O CHC.sub.2 H.sub.5157 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5158 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5159 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5160 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5161 2,6-F.sub.2C.sub.6 H.sub.3 CH.sub.2 O CHC.sub.2 H.sub.5162 2-Pyridyl-methoxy CHC.sub.2 H.sub.5163 t-C.sub.4 H.sub.9(CH.sub.3).sub.2SiO CHC.sub.2 H.sub.5164 CH.sub.3 NH CHC.sub.2 H.sub.5165 C.sub.6 H.sub.5 NH CHC.sub.2 H.sub.5166 2-CH.sub.3 C.sub.6 H.sub.4 NH CHC.sub.2 H.sub.5167 2-ClC.sub.6 H.sub.4 NH CHC.sub.2 H.sub.5168 3-CH.sub.3 OC.sub.6 H.sub.4 NH CHC.sub.2 H.sub.5169 4-Cyano-C.sub.6 H.sub.4 NH CHC.sub.2 H.sub.5170 2,6-F.sub.2C.sub.6 H.sub.3 NH CHC.sub.2 H.sub.5171 C.sub.6 H.sub.5 NCH.sub.3 CHC.sub.2 H.sub.5172 2-ClC.sub.6 H.sub.4 NCH.sub.3 CHC.sub.2 H.sub.5173 4-Cyano-C.sub.6 H.sub.4 NCH.sub.3 CHC.sub.2 H.sub.5174 C.sub.6 H.sub.5 CH.sub.2 NH CHC.sub.2 H.sub.5175 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 NH CHC.sub.2 H.sub.5176 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHC.sub.2 H.sub.5177 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 NH CHC.sub.2 H.sub.5178 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NH CHC.sub.2 H.sub.5179 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 NH CHC.sub.2 H.sub.5180 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHC.sub.2 H.sub.5181 2-ClC.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 CHC.sub.2 H.sub.5182 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 NCH.sub.3 CHC.sub.2 H.sub.5183 HS CHC.sub.2 H.sub.5184 C.sub.6 H.sub.5 CH.sub.2 S CHC.sub.2 H.sub.5__________________________________________________________________________ TABLE X__________________________________________________________________________ ##STR20## Iso- m.p.No. A B X mer (.degree.C.) .delta. (C .sub.--H.sub.2 C .sub.--H.sub.2)__________________________________________________________________________1 H CH.sub.3 CHOCH.sub.32 H t-C.sub.4 H.sub.9 CHOCH.sub.33 H C.sub.6 H.sub.5 CHOCH.sub.34 H 2-CH.sub.3 C.sub.6 H.sub.4 CHOCH.sub.35 H 4-Cyano-C.sub.6 H.sub.4 CHOCH.sub.36 H 2,6-F.sub.2 C.sub.6 H.sub.3 CHOCH.sub.37 CH.sub.3 CH.sub.3 CHOCH.sub.38 CH.sub.3 t-C.sub.4 H.sub.9 CHOCH.sub.39 CH.sub.3 C.sub.6 H.sub.5 CHOCH.sub.310 CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 CHOCH.sub.311 CH.sub.3 4-Cyano-C.sub.6 H.sub.4 CHOCH.sub.312 CH.sub.3 2,6-F.sub.2 C.sub.6 H.sub.3 CHOCH.sub.313 C.sub.6 H.sub. 5 CH.sub.3 CHOCH.sub.314 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CHOCH.sub.315 C.sub.6 H.sub.5 2,6-F.sub.2 C.sub.6 H.sub.3 CHOCH.sub.316 H HO CHOCH.sub.317 H CH.sub.3 O CHOCH.sub.318 H t-C.sub.4 H.sub.9 O CHOCH.sub.319 H H.sub.2 CCClCH.sub.2 O CHOCH.sub.320 H C.sub.6 H.sub.5 CH.sub.2 O CHOCH.sub.321 H 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.322 H 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.323 H 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.324 H 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.325 H 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O CHOCH.sub.326 H 3-Pyridylmethoxy CHOCH.sub.327 H 5-Chlorothien-2-ylme- CHOCH.sub.3 thoxy28 H CH.sub.3 CO CHOCH.sub.329 H C.sub.6 H.sub.5 CO CHOCH.sub.330 CH.sub.3 HO CHOCH.sub.331 CH.sub.3 CH.sub.3 O CHOCH.sub.332 CH.sub.3 t-C.sub.4 H.sub.9 O CHOCH.sub.333 CH.sub.3 H.sub.2 CCClCH.sub.2 O CHOCH.sub.334 CH.sub.3 C.sub. 6 H.sub.5 CH.sub.2 O CHOCH.sub.335 CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.336 CH.sub.3 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.337 CH.sub.3 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.338 CH.sub.3 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHOCH.sub.339 CH.sub.3 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O CHOCH.sub.340 CH.sub.3 3-Pyridylmethoxy CHOCH.sub.341 CH.sub.3 5-Chlorothien-2-ylme- CHOCH.sub.3 thoxy42 CH.sub.3 CH.sub.3 CO CHOCH.sub.343 CH.sub.3 C.sub.6 H.sub.5 CO CHOCH.sub.344 C.sub.6 H.sub.5 HO CHOCH.sub.345 C.sub.6 H.sub.5 CH.sub.3 O CHOCH.sub.346 C.sub.6 H.sub.5 H.sub.2 CCClCH.sub.2 O CHOCH.sub.347 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CH.sub.2 O CHOCH.sub.348 C.sub.6 H.sub.5 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O CHOCH.sub.349 C.sub.6 H.sub.5 CH.sub.3 O CHOCH.sub.350 H CH.sub.3 NH CHOCH.sub.351 H (CH.sub.3).sub.2 N CHOCH.sub.352 H C.sub.6 H.sub.5 NH CHOCH.sub.353 H 2-ClC.sub.6 H.sub.4 NH CHOCH.sub.354 H C.sub.6 H.sub.5 NCH.sub.3 CHOCH.sub.355 H C.sub.6 H.sub.5 CH.sub.2 NH CHOCH.sub.356 H 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHOCH.sub.357 H C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHOCH.sub.358 H CH.sub.3 CO CHOCH.sub.359 H C.sub.6 H.sub.5 CO CHOCH.sub.360 CH.sub.3 CH.sub.3 NH CHOCH.sub.361 CH.sub.3 (CH.sub.3).sub.2 N CHOCH.sub.362 CH.sub.3 C.sub.6 H.sub.5 NH CHOCH.sub.363 CH.sub.3 2-ClC.sub.6 H.sub.4 NH CHOCH.sub.364 CH.sub.3 C.sub.6 H.sub.5 NCH.sub.3 CHOCH.sub.365 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 NH CHOCH.sub.366 CH.sub.3 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHOCH.sub.367 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHOCH.sub.368 CH.sub.3 CH.sub.3 CO CHOCH.sub.369 CH.sub.3 C.sub.6 H.sub.5 CO CHOCH.sub.370 C.sub.6 H.sub.5 CH.sub.3 NH CHOCH.sub.371 C.sub.6 H.sub.5 (CH.sub. 3).sub.2 N CHOCH.sub.372 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NH CHOCH.sub.373 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NCH.sub.3 CHOCH.sub.374 C.sub.6 H.sub.5 CH.sub.3 CO CHOCH.sub.375 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CO CHOCH.sub.376 H CH.sub.3 NOCH.sub.377 H t-C.sub.4 H.sub.9 NOCH.sub.378 H C.sub.6 H.sub.5 NOCH.sub.379 H 2-CH.sub.3 C.sub.6 H.sub.4 NOCH.sub.380 H 4-Cyano-C.sub.6 H.sub.4 NOCH.sub.381 H 2,6-F.sub.2 C.sub.6 H.sub.3 NOCH.sub.382 CH.sub.3 CH.sub.3 NOCH.sub.383 CH.sub.3 t-C.sub.4 H.sub.9 NOCH.sub.384 CH.sub.3 C.sub.6 H.sub.5 NOCH.sub.385 CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 NOCH.sub.386 CH.sub.3 4-Cyano-C.sub.6 H.sub.4 NOCH.sub.387 CH.sub.3 2,6-F.sub.2 C.sub.6 H.sub.3 NOCH.sub.388 C.sub.6 H.sub.5 CH.sub.3 NOCH.sub.389 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NOCH.sub.390 C.sub.6 H.sub.5 2,6-F.sub.2 C.sub.6 H.sub.3 NOCH.sub.391 H HO NOCH.sub.392 H CH.sub.3 O NOCH.sub.393 H t-C.sub.4 H.sub.9 O NOCH.sub.394 H H.sub.2 CCClCH.sub.2 O NOCH.sub.395 H C.sub.6 H.sub.5 CH.sub.2 O NOCH.sub.396 H 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.397 H 2-ClC.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.398 H 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.399 H 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.3100 H 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O NOCH.sub.3101 H 3-Pyridylmethoxy NOCH.sub.3102 H 5-Chlorothien-2-ylme- NOCH.sub.3 thoxy103 H CH.sub.3 CO NOCH.sub.3104 H C.sub.6 H.sub.5 CO NOCH.sub.3105 CH.sub.3 HO NOCH.sub.3106 CH.sub.3 CH.sub.3 O NOCH.sub.3107 CH.sub.3 t-C.sub.4 H.sub.9 O NOCH.sub.3108 CH.sub.3 H.sub.2 CCClCH.sub.2 O NOCH.sub.3109 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 O NOCH.sub.3110 CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.3111 CH.sub.3 2-ClC.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.3112 CH.sub.3 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.3113 CH.sub.3 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O NOCH.sub.3114 CH.sub.3 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O NOCH.sub.3115 CH.sub.3 3-Pyridylmethoxy NOCH.sub.3116 CH.sub.3 5-Chlorothien-2-ylme- NOCH.sub.3 thoxy117 CH.sub.3 CH.sub.3 CO NOCH.sub.3118 CH.sub.3 C.sub.6 H.sub.5 CO NOCH.sub.3119 C.sub.6 H.sub.5 HO NOCH.sub.3120 C.sub.6 H.sub.5 CH.sub.3 O NOCH.sub.3121 C.sub.6 H.sub.5 H.sub.2 CCClCH.sub.2 O NOCH.sub.3122 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CH.sub.2 O NOCH.sub.3123 C.sub.6 H.sub.5 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O NOCH.sub.3124 C.sub.6 H.sub.5 CH.sub.3 O NOCH.sub.3125 H CH.sub.3 NH NOCH.sub.3126 H (CH.sub.3).sub.2 N NOCH.sub.3127 H C.sub.6 H.sub.5 NH NOCH.sub.3128 H 2-ClC.sub.6 H.sub.4 NH NOCH.sub.3129 H C.sub.6 H.sub.5 NCH.sub.3 NOCH.sub.3130 H C.sub.6 H.sub.5 CH.sub.2 NH NOCH.sub.3131 H 2-ClC.sub.6 H.sub.4 CH.sub.2 NH NOCH.sub.3132 H C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 NOCH.sub.3133 H CH.sub.3 CO NOCH.sub.3134 H C.sub.6 H.sub.5 CO NOCH.sub.3135 CH.sub.3 CH.sub.3 NH NOCH.sub.3136 CH.sub.3 (CH.sub.3).sub.2 N NOCH.sub.3137 CH.sub.3 C.sub.6 H.sub.5 NH NOCH.sub.3138 CH.sub.3 2-ClC.sub.6 H.sub.4 NH NOCH.sub.3139 CH.sub.3 C.sub.6 H.sub.5 NCH.sub.3 NOCH.sub.3140 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 NH NOCH.sub.3141 CH.sub.3 2-ClC.sub.6 H.sub.4 CH.sub.2 NH NOCH.sub.3142 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 NOCH.sub.3143 CH.sub.3 CH.sub.3 CO NOCH.sub.3144 CH.sub.3 C.sub.6 H.sub.5 CO NOCH.sub.3145 C.sub.6 H.sub.5 CH.sub.3 NH NOCH.sub.3146 C.sub.6 H.sub.5 (CH.sub.3).sub.2 N NOCH.sub.3147 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NH NOCH.sub.3148 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NCH.sub.3 NOCH.sub.3149 C.sub.6 H.sub.5 CH.sub.3 CO NOCH.sub.3150 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CO NOCH.sub.3151 H CH.sub.3 CHCH.sub.3152 H t-C.sub.4 H.sub.9 CHCH.sub.3153 H C.sub.6 H.sub.5 CHCH.sub.3154 H 2-CH.sub.3 C.sub.6 H.sub.4 CHCH.sub.3155 H 4-Cyano-C.sub.6 H.sub.4 CHCH.sub.3156 H 2,6-F.sub.2 C.sub.6 H.sub.3 CHCH.sub.3157 CH.sub.3 CH.sub.3 CHCH.sub.3158 CH.sub.3 t-C.sub.4 H.sub.9 CHCH.sub.3159 CH.sub.3 C.sub.6 H.sub.5 CHCH.sub.3160 CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 CHCH.sub.3161 CH.sub.3 4-Cyano-C.sub.6 H.sub.4 CHCH.sub.3162 CH.sub.3 2,6-F.sub.2 C.sub.6 H.sub.3 CHCH.sub.3163 C.sub.6 H.sub.5 CH.sub.3 CHCH.sub.3164 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CHCH.sub.3165 C.sub.6 H.sub.5 2,6-F.sub.2 C.sub.6 H.sub.3 CHCH.sub.3166 H HO CHCH.sub.3167 H CH.sub.3 O CHCH.sub.3168 H t-C.sub.4 H.sub.9 O CHCH.sub.3169 H H.sub.2 CCClCH.sub.2 O CHCH.sub.3170 H C.sub.6 H.sub.5 CH.sub.2 O CHCH.sub.3171 H 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3172 H 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3173 H 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3174 H 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3175 H 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O CHCH.sub.3176 H 3-Pyridylmethoxy CHCH.sub.3177 H 5-Chlorothien-2-ylme- CHCH.sub.3 thoxy178 H CH.sub.3 CO CHCH.sub.3179 H C.sub.6 H.sub.5 CO CHCH.sub.3180 CH.sub.3 HO CHCH.sub.3181 CH.sub.3 CH.sub.3 O CHCH.sub.3182 CH.sub.3 t-C.sub.4 H.sub.9 O CHCH.sub.3183 CH.sub.3 H.sub.2 CCClCH.sub.2 O CHCH.sub.3184 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 O CHCH.sub.3185 CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3186 CH.sub.3 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3187 CH.sub.3 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3188 CH.sub.3 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3189 CH.sub.3 2,6-F.sub.2 C.sub.6 H.sub.4 CH.sub.2 O CHCH.sub.3190 CH.sub.3 3-Pyridylmethoxy CHCH.sub.3191 CH.sub.3 5-Chlorothien-2-ylme- CHCH.sub.3 thoxy192 CH.sub.3 CH.sub.3 CO CHCH.sub.3193 CH.sub.3 C.sub.6 H.sub.5 CO CHCH.sub.3194 C.sub.6 H.sub.5 HO CHCH.sub.3195 C.sub.6 H.sub.5 CH.sub.3 O CHCH.sub.3196 C.sub.6 H.sub.5 H.sub.2 CCClCH.sub.2 O CHCH.sub.3197 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CH.sub.2 O CHCH.sub.3198 C.sub.6 H.sub.5 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O CHCH.sub.3199 C.sub.6 H.sub.5 CH.sub.3 O CHCH.sub.3200 H CH.sub.3 NH CHCH.sub.3201 H (CH.sub.3).sub.2 N CHCH.sub.3202 H C.sub.6 H.sub.5 NH CHCH.sub.3203 H 2-ClC.sub.6 H.sub.4 NH CHCH.sub.3204 H C.sub.6 H.sub.5 NCH.sub.3 CHCH.sub.3205 H C.sub.6 H.sub.5 CH.sub.2 NH CHCH.sub.3206 H 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHCH.sub.3207 H C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHCH.sub.3208 H CH.sub.3 CO CHCH.sub.3209 H C.sub.6 H.sub.5 CO CHCH.sub.3210 CH.sub.3 CH.sub.3 NH CHCH.sub.3211 CH.sub.3 (CH.sub.3).sub.2 N CHCH.sub.3212 CH.sub.3 C.sub.6 H.sub.5 NH CHCH.sub.3213 CH.sub.3 2-ClC.sub.6 H.sub.4 NH CHCH.sub.3214 CH.sub.3 C.sub.6 H.sub.5 NCH.sub.3 CHCH.sub.3215 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 NH CHCH.sub.3216 CH.sub.3 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHCH.sub.3217 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHCH.sub.3218 CH.sub.3 CH.sub.3 CO CHCH.sub.3219 CH.sub.3 C.sub.6 H.sub.5 CO CHCH.sub.3220 C.sub.6 H.sub.5 CH.sub.3 NH CHCH.sub.3221 C.sub.6 H.sub.5 (CH.sub.3).sub.2 N CHCH.sub.3222 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NH CHCH.sub.3223 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NCH.sub.3 CHCH.sub.3224 C.sub.6 H.sub.5 CH.sub.3 CO CHCH.sub.3225 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CO CHCH.sub.3226 H CH.sub.3 CHC.sub.2 H.sub.5227 H t-C.sub.4 H.sub.9 CHC.sub.2 H.sub.5228 H C.sub.6 H.sub.5 CHC.sub.2 H.sub.5229 H 2-CH.sub.3 C.sub.6 H.sub.4 CHC.sub.2 H.sub.5230 H 4-Cyano-C.sub.6 H.sub.4 CHC.sub.2 H.sub.5231 H 2,6-F.sub.2 C.sub.6 H.sub.3 CHC.sub.2 H.sub.5232 CH.sub.3 CH.sub.3 CHC.sub.2 H.sub.5233 CH.sub.3 t-C.sub.4 H.sub.9 CHC.sub.2 H.sub.5234 CH.sub.3 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5235 CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 CHC.sub.2 H.sub.5236 CH.sub.3 4-Cyano-C.sub.6 H.sub.4 CHC.sub.2 H.sub.5237 CH.sub.3 2,6-F.sub.2 C.sub.6 H.sub.3 CHC.sub.2 H.sub.5238 C.sub.6 H.sub.5 CH.sub.3 CHC.sub.2 H.sub.5239 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CHC.sub.2 H.sub.5240 C.sub.6 H.sub.5 2,6-F.sub.2 C.sub.6 H.sub.3 CHC.sub.2 H.sub.5241 H HO CHC.sub.2 H.sub.5242 H CH.sub.3 O CHC.sub.2 H.sub.5243 H t-C.sub.4 H.sub.9 O CHC.sub.2 H.sub.5244 H H.sub.2 CCClCH.sub.2 O CHC.sub.2 H.sub.5245 H C.sub.6 H.sub.5 CH.sub.2 O CHC.sub. 2 H.sub.5246 H 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5247 H 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5248 H 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5249 H 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5250 H 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O CHC.sub.2 H.sub.5251 H 3-Pyridylmethoxy CHC.sub.2 H.sub.5252 H 5-Chlorothien-2-ylme- CHC.sub.2 H.sub.5 thoxy253 H CH.sub.3 CO CHC.sub.2 H.sub.5254 H C.sub.6 H.sub.5 CO CHC.sub.2 H.sub.5255 CH.sub.3 HO CHC.sub.2 H.sub.5256 CH.sub.3 CH.sub.3 O CHC.sub.2 H.sub.5257 CH.sub.3 t-C.sub.4 H.sub.9 O CHC.sub.2 H.sub.5258 CH.sub.3 H.sub.2 CCClCH.sub.2 O CHC.sub.2 H.sub.5259 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 O CHC.sub.2 H.sub.5260 CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5261 CH.sub.3 2-ClC.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5262 CH.sub.3 3-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5263 CH.sub.3 4-Cyano-C.sub.6 H.sub.4 CH.sub.2 O CHC.sub.2 H.sub.5264 CH.sub.3 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O CHC.sub.2 H.sub.5265 CH.sub.3 3-Pyridylmethoxy CHC.sub.2 H.sub.5266 CH.sub.3 5-Chlorothien-2-ylme- CHC.sub.2 H.sub.5 thoxy267 CH.sub.3 CH.sub.3 CO CHC.sub.2 H.sub.5268 CH.sub.3 C.sub.6 H.sub.5 CO CHC.sub.2 H.sub.5269 C.sub.6 H.sub.5 HO CHC.sub.2 H.sub.5270 C.sub.6 H.sub.5 CH.sub.3 O CHC.sub.2 H.sub.5271 C.sub.6 H.sub.5 H.sub.2 CCClCH.sub.2 O CHC.sub.2 H.sub.5272 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CH.sub.2 O CHC.sub.2 H.sub.5273 C.sub.6 H.sub.5 2,6-F.sub.2 C.sub.6 H.sub.3 CH.sub.2 O CHC.sub.2 H.sub.5274 C.sub.6 H.sub.5 CH.sub.3 O CHC.sub.2 H.sub.5275 H CH.sub.3 NH CHC.sub.2 H.sub.5276 H (CH.sub.3).sub.2 N CHC.sub.2 H.sub.5277 H C.sub.6 H.sub.5 NH CHC.sub.2 H.sub.5278 H 2-ClC.sub.6 H.sub.4 NH CHC.sub.2 H.sub.5279 H C.sub.6 H.sub.5 NCH.sub.3 CHC.sub.2 H.sub.5280 H C.sub.6 H.sub.5 CH.sub.2 NH CHC.sub.2 H.sub.5281 H 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHC.sub.2 H.sub.5282 H C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHC.sub.2 H.sub.5283 H CH.sub.3 CO CHC.sub.2 H.sub.5284 H C.sub.6 H.sub.5 CO CHC.sub.2 H.sub.5285 CH.sub.3 CH.sub.3 NH CHC.sub.2 H.sub.5286 CH.sub.3 (CH.sub.3).sub.2 N CHC.sub.2 H.sub.5287 CH.sub.3 C.sub.6 H.sub.5 NH CHC.sub.2 H.sub.5288 CH.sub.3 2-ClC.sub.6 H.sub.4 NH CHC.sub.2 H.sub.5289 CH.sub.3 C.sub.6 H.sub.5 NCH.sub.3 CHC.sub.2 H.sub.5290 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 NH CHC.sub.2 H.sub.5291 CH.sub.3 2-ClC.sub.6 H.sub.4 CH.sub.2 NH CHC.sub.2 H.sub.5292 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 NCH.sub.3 CHC.sub.2 H.sub.5293 CH.sub.3 CH.sub.3 CO CHC.sub.2 H.sub.5294 CH.sub.3 C.sub.6 H.sub.5 CO CHC.sub.2 H.sub.5295 C.sub.6 H.sub.5 CH.sub.3 NH CHC.sub.2 H.sub.5296 C.sub.6 H.sub.5 (CH.sub.3).sub.2 N CHC.sub.2 H.sub.5297 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NH CHC.sub.2 H.sub.5298 C.sub.6 H.sub.5 C.sub.6 H.sub.5 NCH.sub.3 CHC.sub.2 H.sub.5299 C.sub.6 H.sub.5 CH.sub.3 CO CHC.sub.2 H.sub.5300 C.sub.6 H.sub.5 C.sub.6 H.sub.5 CO CHC.sub.2 H.sub.5__________________________________________________________________________ TABLE XI__________________________________________________________________________ ##STR21## Iso- m.p.No. R X mer (.degree.C.) .delta.(CC .sub.--H)__________________________________________________________________________1 H CHOCH.sub.32 CH.sub.3 CHOCH.sub.33 C.sub.2 H.sub.5 CHOCH.sub.34 i-C.sub.3 H.sub.7 CHOCH.sub.35 t-C.sub.4 H.sub.9 CHOCH.sub.3 a oil 6.656 Allyl CHOCH.sub.37 2-Chloroallyl CHOCH.sub.38 2-Methylallyl CHOCH.sub.39 Benzyl CHOCH.sub.310 2-Methoxybenzyl CHOCH.sub.311 3-Trifluoromethylbenzyl CHOCH.sub.312 4-Methylbenzyl CHOCH.sub.313 3,5-Dichlorobenzyl CHOCH.sub.314 (2-Pyridyl)-methyl CHOCH.sub.315 5-Chlorothien-2-ylmethyl CHOCH.sub.316 H NOCH.sub.317 CH.sub.3 NOCH.sub.318 C.sub.2 H.sub.5 NOCH.sub.319 i-C.sub.3 H.sub.7 NOCH.sub.320 t-C.sub.4 H.sub.9 NOCH.sub.3 a oil 6.6221 Allyl NOCH.sub.322 2-Chloroallyl NOCH.sub.323 2-Methylallyl NOCH.sub.324 Benzyl NOCH.sub.325 2-Methoxybenzyl NOCH.sub.326 3-Trifluoromethylbenzyl NOCH.sub.3 a oil 6.7227 4-Methylbenzyl NOCH.sub.328 3,5-Dichlorobenzyl NOCH.sub.329 (2-Pyridyl)-methyl NOCH.sub.330 5-Chlorothien-2-ylmethyl NOCH.sub.331 H CHCH.sub.332 CH.sub.3 CHCH.sub.333 C.sub.2 H.sub.5 CHCH.sub.334 i-C.sub.3 H.sub.7 CHCH.sub.335 t-C.sub.4 H.sub.9 CHCH.sub.336 Allyl CHCH.sub.337 2-Chloroallyl CHCH.sub.338 2-Methylallyl CHCH.sub.339 Benzyl CHCH.sub.340 2-Methoxybenzyl CHCH.sub.341 3-Trifluoromethylbenzyl CHCH.sub.342 4-Methylbenzyl CHCH.sub.343 3,5-Dichlorobenzyl CHCH.sub.344 (2-Pyridyl)-methyl CHCH.sub.345 5-Chlorothien-2-ylmethyl CHCH.sub.346 H CHC.sub.2 H.sub.547 CH.sub.3 CHC.sub.2 H.sub.548 C.sub.2 H.sub.5 CHC.sub.2 H.sub.549 i-C.sub.3 H.sub.7 CHC.sub.2 H.sub.550 t-C.sub.4 H.sub.9 CHC.sub.2 H.sub.551 Allyl CHC.sub.2 H.sub.552 2-Chloroallyl CHC.sub.2 H.sub.553 2-Methylallyl CHC.sub.2 H.sub.554 Benzyl CHC.sub.2 H.sub.555 2-Methoxybenzyl CHC.sub.2 H.sub.556 3-Trifluoromethylbenzyl CHC.sub.2 H.sub.557 4-Methylbenzyl CHC.sub.2 H.sub.558 3,5-Dichlorobenzyl CHC.sub.2 H.sub.559 (2-Pyridyl)-methyl CHC.sub.2 H.sub.560 5-Chlorothien-2-ylmethyl CHC.sub.2 H.sub.5__________________________________________________________________________ The novel compounds are suitable as fungicides.

The fungicidal compounds I, or agents containing them, may be applied for instance in the form of directly sprayable solutions, powders, suspensions (including high-percentage aqueous, oily or other suspensions), dispersions, emulsions, oil dispersions, pastes, dusts, broadcasting agents, or granules by spraying, atomizing, dusting, broadcasting or watering. The forms of application depend entirely on the purpose for which the agents are being used, but they must ensure as fine a distribution of the active ingredients according to the invention as possible.

Normally, the plants are sprayed or dusted with the active ingredients, or the seeds of the plants are treated with the active ingredients.

The formulations are produced in known manner, for example by extending the active ingredient with solvents and/or carriers, with or without the use of emulsifiers and dispersants; if water is used as solvent, it is also possible to employ other organic solvents as auxiliary solvents. Suitable auxiliaries for this purpose are solvents such as aromatics (e.g., xylene), chlorinated aromatics (e.g., chlorobenzenes), paraffins (e.g., crude oil fractions), alcohols (e.g., methanol, butanol), ketones (e.g., cyclohexanone), amines (e.g., ethanolamine, dimethylformamide), and water; carriers such as ground natural minerals (e.g., kaolins, aluminas, talc and chalk) and ground synthetic minerals (e.g., highly disperse silica and silicates); emulsifiers such as nonionic and anionic emulsifiers (e.g., polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates); and dispersants such as lignin-sulfite waste liquors and methylcellulose.

Examples of surfactants are: alkali metal, alkaline earth metal and ammonium salts of aromatic sulfonic acids, e.g., ligninsulfonic acid, phenolsulfonic acid, naphthalenesulfonic acid and dibutylnaphthalenesulonic acid, and of fatty acids, alkyl and alkylaryl sulfonates, and alkyl, lauryl ether and fatty alcohol sulfates, and salts of sulfated hexadecanols, heptadecanols, and octadecanols, salts of fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensation products of naphthalene or naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ethers, ethoxylated isooctylphenol, ethoxylated octylphenol and ethoxylated nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ethers, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignin-sulfite waste liquors and methyl cellulose.

Powders, dusts and broadcasting agents may be prepared by mixing or grinding the active ingredients with a solid carrier.

Granules, e.g., coated, impregnated or homogeneous granules, may be prepared by bonding the active ingredients to solid carriers. Examples of solid carriers are mineral earths such as silicic acids, silica gels, silicates, talc, kaolin, attapulgus clay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground plastics, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, and ureas, and vegetable products such as grain meals, bark meal, wood meal, and nutshell meal, cellulosic powders, etc.

Examples of formulations are as follows:

I. A solution of 90 parts by weight of compound no. 2 and 10 parts by weight of N-methyl-.alpha.-pyrrolidone, which is suitable for application in the form of very fine drops.

II. A mixture of 20 parts by weight of compound no. 1/110, 80 parts by weight of xylene, 10 parts by weight of the adduct of 8 to 10 moles of ethylene oxide and 1 mole of oleic acid-N-monoethanolamide, 5 parts by weight of the calcium salt of dodecylbenzenesulfonic acid, and 5 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By finely dispersing the mixture in water, an aqueous dispersion is obtained.

III. An aqueous dispersion of 20 parts by weight of compound no. 6/22, 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil.

IV. An aqueous dispersion of 20 parts by weight of compound no. 6/27, 25 parts by weight of cyclohexanol, 65 parts by weight of a mineral oil fraction having a boiling point between 210.degree. and 280.degree. C., and 10 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil.

V. A hamer-milled mixture of 80 parts by weight of compound no. 6/72, 3 parts by weight of the sodium salt of diisobutylnaphthalene-.alpha.-sulfonic acid, 10 parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 7 parts by weight of powdered silica gel. By finely dispersing the mixture in water, a spray liquor is obtained.

VI. An intimate mixture of 3 parts by weight of compound no. 6/77 and 97 parts by weight of particulate kaolin. The dust contains 3 wt % of the active ingredient.

VII. An intimate mixture of 30 parts by weight of compound no. 6/78, 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil sprayed onto the surface of this silica gel. This formulation of the active ingredient exhibits good adherence.

VIII. A stable aqueous dispersion of 40 parts by weight of compound no. 6/83, 10 parts of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate, 2 parts of silica gel and 48 parts of water, which dispersion can be further diluted.

IX. A stable oily dispersion of 20 parts by weight of compound no. 6/85, 2 parts by weight of the calcium salt of dodecylbenzenesulfonic acid, 8 parts by weight of a fatty alcohol polyglycol ether, 2 parts by weight of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate and 68 parts by weight of a paraffinic mineral oil.

The novel compounds are extremely effective on a broad spectrum of phytopathogenic fungi, in particular those from the class consisting of the Ascomycetes and Basidiomycetes. Some of them have a systemic action and can be used as foliar and soil fungicides.

The fungicidal compounds are of particular interest for controlling a large number of fungi in various crops or their seeds, especially wheat, rye, barley, oats, rice, Indian corn, lawns, cotton, soybeans, coffee, sugar cane, fruit and ornamentals in horticulture and viticulture, and in vegetables such as cucumbers, beans and cucurbits.

The compounds are applied by treating the fungi, or the seed, plants or materials threatened by fungus attack, or the soil with a fungicidally effective amount of the active ingredients.

Application is effected before or after infection of the materials, plants or seed by the fungi.

The compounds I are particularly useful for controlling the following plant diseases:

Erysiphe graminis in cereals, Erysiphe cichoracearum and Sphaerotheca fuliginea in cucurbits, Podosphaera leucotricha in apples, Uncinula necator in vines, Puccinia species in cereals, Rhizoctonia solani in cotton, Ustilago species in cereals and sugar cane, Venturia inaequalis (scab) in apples, Helminthosporium species in cereals, Septoria nodorum in wheat, Botrytis cinerea (gray mold) in strawberries and grapes, Cercospora arachidicola in groundnuts, Pseudocercosporella herpotrichoides in wheat and barley, Pyricularia oryzae in rice, Phytophthora infestans in potatoes and tomatoes, Fusarium and Verticillium species in various plants, Plasmopara viticola in grapes, Alternaria species in fruit and vegetables.

The novel compounds may also be used for protecting materials (timber), e.g., against Paecilomyces variotii.

The fungicidal agents generally contain from 0.1 to 95, and preferably from 0.5 to 90, wt % of active ingredient.

The application rates depend on the type of effect desired, and range from 0.02 to 3 kg of active ingredient per hectare.

When the active ingredients are used for treating seed, rates of 0.001 to 50, and preferably from 0.01 to 10, g per kg of seed are generally required.

When the agents according to the invention are used as fungicides, they may be present together with other active ingredients such as herbicides, insecticides, growth regulators, other fungicides, or fertilizers.

When the agents according to the invention are mixed with other fungicides, the spectrum of fungicidal action is frequently increased.

The active ingredient used for comparison purposes was methyl 2-(2-methylphenyl)-2-methoxyacrylate (A)-disclosed in EP 178 826.

USE EXAMPLES

Use Example 1

Action on wheat mildew

Leaves of pot-grown wheat seedlings of the "Fruhgold" variety were sprayed with aqueous liquors containing (dry basis) 80% of active ingredient and 20% of emulsifier, and dusted, 24 hours after the sprayed-on layer had dried, with spores of wheat mildew (Erysiphe graminis var. tritici). The plants were then set up in the greenhouse at from 20.degree. to 22.degree. C. and a relative humidity of from 75 to 80%. The extent of mildew spread was assessed after 7 days.

The results show that active ingredients 2 from Table 1 (1/2), 1/110, 6/22, 6/27, 6/72, 6/77, 6/78, 6/83, 6/85, 6/89, 6/90, 7/36, 7/41a, 7/41s, 7/43, 7/60, 7/106, 7/107, 7/111, 7/112, 7/113, 7/116, 7/130 and 7/133, when applied as spray liquors containing the active ingredients in amounts of 250 ppm, have a better fungicidal action (90%) than prior art comparative compound A (50%).

Use Example 2

Action on Plasmopara viticola

Leaves of potted vines of the Muller-Thurgau variety were sprayed with aqueous suspensions containing (dry basis) 80% of active ingredient and 20% of emulsifier. To assess the duration of action, the plants were set up, after the sprayed-on layer had dried, for 8 days in the greenhouse. Then the leaves were infected with a zoospore suspension of Plasmopara viticola. The plants were first placed for 48 hours in a water vapor-saturated chamber at 24.degree. C. and then in a greenhouse for 5 days at from 20.degree. to 30.degree. C. To accelerate and intensify the sporangiophore discharge, the plants were then again placed in the moist chamber for 16 hours. The extent of fungus attack was then assessed on the undersides of the leaves.

The results show that active ingredients 1/2, 1/12, 1/88, 1(115, 2/57, 3/55, 6/22, 6/27, 6/72, 6/77, 6/78, 6/83, 6/85, 6/89, 6/90, 6/97, 7/36, 7/41a, 7/41s, 7/43, 7/60, 7/106, 7/112, 7/113, 7/116, 7/130, 7/133, 8/70 and 9/50, when applied as spray liquors containing 250 ppm of active ingredient, have a better fungicidal action (90%) than prior art comparative agent A (0%).

Claims

1. A compound of the formula I ##STR22## where n is 0 or 1,

W is hydrogen, halogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy,

X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3 or CHC.sub.2 H.sub.5,

Y is oxygen, sulfur or NR.sup.4, --O--NR.sup.4 --, --NR.sup.4 --O-- or --NR.sup.4 --NR.sup.5 --,

Z is oxygen, NR.sup.6, NOR.sup.7 or N--NR.sup.8 R.sup.9 or, where n=1, sulfur,

R.sup.1 is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl,

R.sup.2 is independent of R.sup.1 and is hydrogen unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted aryl, C.sub.1 -C.sub.4 -perfluoroalkyl or CO--V

R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, or unsubstituted or substituted aryl-C.sub.2 -C.sub.4 -alkenyl or, where n=0, cyano, C.sub.1 -C.sub.4 -perfluoroalkyl or unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl or, where n=1, and Y is oxygen, unsubstituted or substituted trialkylsilyl,

R.sup.4 and R.sup.5 are independent of one another and are each hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl,

R.sup.6 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, or unsubstituted or substituted or fused aryl,

R.sup.7 and R.sup.8 are each hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, or COR.sup.10,

R.sup.9 has the same meanings as R.sup.4 and is independent of R.sup.8,

R.sup.10 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, or unsubstituted or substituted aryl,

V is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted aryl, hydroxyl, unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy, unsubstituted or substituted allyloxy, unsubstituted or substituted benzyloxy or unsubstituted or substituted trialkylsilyloxy

and is a single bond or a double bond.

2. A compound as claimed in claim 1, wherein X is CHOCH.sub.3.

3. A compound as claimed in claim 1, wherein X is NOCH.sub.3.

4. A compound as claimed in claim 1, wherein X is CHCH.sub.3 or CHC.sub.2 H.sub.5.

5. A compound as claimed in claim 1, wherein the bond between the carbon atoms substituted by R.sup.1 and R.sup.2 is a single bond.

6. A compound as claimed in claim 1, wherein the bond between the carbon atoms substituted by R.sup.1 and R.sup.2 is a double bond.

7. A compound of the formula I as claimed in claim 1, wherein n is 0 and R.sup.3 --(Y).sub.n --C.dbd.Z is ##STR23##

8. A compound of the formula I as claimed in claim 1, wherein n is 1 and R.sup.3 --(Y).sub.n --C.dbd.Z is ##STR24##

9. A compound of the formula II ##STR25## where W is hydrogen, chlorine, methyl or methoxy,

X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3, or CHC.sub.2 H.sub.5,

Z is oxygen, NR.sup.6, NOR.sup.7 or N--NR.sup.8 R.sup.9,

R.sup.1 and R.sup.2 are independent of one another and are each hydrogen or C.sub.1 -C.sub.4 -alkyl,

R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, or unsubstituted or substituted aryl-C.sub.2 -C.sub.4 -alkenyl

R.sup.4 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl,

R.sup.6 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted or fused aryl,

R.sup.7 and R.sup.8 are each hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, or COR.sup.10,

R.sup.9 has the same meanings as R.sup.4 and is independent of R.sup.8 and

R.sup.10 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, or unsubstituted or substituted aryl.

10. A compound of the formula III ##STR26## where W is hydrogen, chlorine, methyl or methoxy,

X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3, or CHC.sub.2 H.sub.5,

Y is oxygen, sulfur or NR.sup.4

R.sup.1 is hydrogen or C.sub.1 -C.sub.4 -alkyl,

R.sup.2 is hydrogen, C.sub.1 -C.sub.4 -alkyl or CO--V ,

R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl

R.sup.4 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl and

V is hydroxyl, C.sub.1 -C.sub.4 -alkoxy, allyloxy, trialkylsilyloxy or unsubstituted or substituted benzyloxy.

11. A compound as claimed in claim 9, wherean X is CHOCH.sub.3.

12. A compound as claimed in claim 9, wherein X is NOCH.sub.3.

13. A compound as claimed in claim 9, wherean X is CHCH.sub.3 or CHC.sub.2 H.sub.5.

14. A compound as claimed in claim 10, wherein X is CHOCH.sub.3.

15. A compound as claimed in claim 10, wherein X is NOCH.sub.3.

16. A compound as claimed in claim 10, wherein X is CHCH.sub.3 or CHC.sub.2 H.sub.5.

17. A compound of the formula IV ##STR27## where X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3, or CHC.sub.2 H.sub.5,

Z is oxygen, NOR.sup.7,

R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, or unsubstituted or substituted or fused aryl,

R.sup.7 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, or COR.sup.10 and

R.sup.10 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, or unsubstituted or substituted aryl.

18. A compound of the formula V ##STR28## where X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3, or CHC.sub.2 H.sub.5,

Y is oxygen, NR.sup.4,

R.sup.3 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted or fused aryl, or unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, and

R.sup.4 is hydrogen or C.sub.1 -C.sub.4 -alkyl.

19. A compound as claimed in claim 17, wherein X is CHOCH.sub.3.

20. A compound as claimed in claim 17, wherein X is NOCH.sub.3.

21. A compound as claimed in claim 17, wherein X is CHCH.sub.3 or CHC.sub.2 H.sub.5.

22. A compound as claimed in claim 18, wherein X is CHOCH.sub.3.

23. A compound as claimed in claim 18, wherein X is NOCH.sub.3.

24. A compound as claimed in claim 18, wherein X is CHCH.sub.3 or CHC.sub.2 H.sub.5.

25. A fungicide which contains an inert carrier and a fungicidal amount of the formula I ##STR29## where n is 0 or 1,

W is hydrogen, halogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy,

X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3 or CHC.sub.2 H.sub.5,

Y is oxygen, sulfur or NR.sup.4, --O--NR.sup.4 --, --NR.sup.4 --O-- or --NR.sup.4 --NR.sup.5 --,

Z is oxygen, NR.sup.6, NOR.sup.7 or N--NR.sup.8 R.sup.9 or, where n=1, sulfur,

R.sup.1 is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl,

R.sup.2 is independent of R.sup.1 and is hydrogen unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted aryl, or C.sub.1 -C.sub.4 -perfluoroalkyl or CO--V

R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted aryl-C.sub.2 -C.sub.4 -alkenyl or, where n=0, cyano, C.sub.1 -C.sub.4 -perfluoroalkyl or unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl or, where n=1, and Y is oxygen, unsubstituted or substituted trialkylsilyl,

R.sup.4 and R.sup.5 are independent of one another and are each hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.3 -C.sub.6 -Cycloalkyl,

R.sup.6 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted or fused aryl,

R.sup.7 and R.sup.8 are each hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, or COR.sup.10,

R.sup.9 has the same meanings as R.sup.4 and is independent of R.sup.8,

R.sup.10 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, or unsubstituted or substituted aryl,

V is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted aryl, hydroxyl, unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy, unsubstituted or substituted allyloxy, unsubstituted or substituted benzyloxy or unsubstituted or substituted trialkylsilyloxy.

26. A method for controlling fungi, wherein a fungicidal amount of a compound of the formula I ##STR30## where n is 0 or 1,

W is hydrogen, halogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy,

X is CHOCH.sub.3, NOCH.sub.3, CHCH.sub.3 or CHC.sub.2 H.sub.5,

Y is oxygen, sulfur or NR.sup.4, --O--NR.sup.4 --, --NR.sup.4 --O-- or --NR.sup.4 --NR.sup.5 --,

Z is oxygen, NR.sup.6, NOR.sup.7 or N--NR.sup.8 R.sup.9 or, where n=1, sulfur,

R.sup.1 is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl,

R.sup.2 is independent of R.sup.1 and is hydrogen unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted aryl, C.sub.1 -C.sub.4 -perfluoroalkyl or CO--V

R.sup.3 is hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted aryl-C.sub.2 -C.sub.4 -alkenyl or, where n=0, cyano, C.sub.1 -C.sub.4 -perfluoroalkyl or unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl or, where n=1, and Y is oxygen, unsubstituted or substituted trialkylsilyl,

R.sup.4 and R.sup.5 are independent of one another and are each hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl or unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl,

R.sup.6 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, or unsubstituted or substituted or fused aryl,

R.sup.7 and R.sup.8 are each hydrogen, unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.1 -C.sub.4 -alkenyl, unsubstituted or substituted C.sub.2 -C.sub.4 -alkynyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, unsubstituted or substituted or fused aryl, unsubstituted or substituted aryl-C.sub.1 -C.sub.4 -alkyl, or COR.sup.10,

R.sup.9 has the same meanings as R.sup.4 and is independent of R.sup.8,

R.sup.10 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted C.sub.3 -C.sub.6 -cycloalkyl, or unsubstituted or substituted aryl,

V is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, unsubstituted or substituted aryl, hydroxyl, unsubstituted or substituted C.sub.1 -C.sub.4 -alkoxy, unsubstituted or substituted allyloxy, unsubstituted or substituted benzyloxy or unsubstituted or substituted trialkylsilyloxy is allowed to act on the fungi or plants, seeds or materials threatened by fungal attack or on the soil.