Use of 4-Aminopyrimidines for Controlling Harmful Fungi, Novel 4-Aminopyrimidines, Processes for Their Preparation and Compositions Comprising Them

The present invention relates to the use of 4-aminopyrimidines of the formula I

in which the substituents are as defined below:

R¹is hydrogen, halogen, cyano, C₁-C₁₄-alkyl, C₁-C₁₄-haloalkyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl, C₃-C₈-cycloalkyl, C₁-C₁₂-alkoxy, C₁-C₁₂-alkoxy-C₁-C₁₂-alkyl, benzyloxy-C₁-C₁₂-alkyl, C₁-C₁₂-alkoxy-C₂-C₁₂-alkenyl or C₁-C₁₂-alkoxy-C₂-C₁₂-alkynyl;
R²is hydrogen, halogen, cyano, C₁-C₁₂-alkyl, C₁-C₁₂-haloalkyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl, C₃-C₈-cycloalkyl, C₁-C₁₂-alkoxy, C₁-C₁₂-alkoxy-C₁-C₁₂-alkyl and C₁-C₁₂-alkylthio-C₁-C₁₂-alkyl,
- where the carbon chains in R¹and/or R²may be substituted by one to four identical or different groups R^α:
- R^αis halogen, cyano, hydroxyl, mercapto, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, C₁-C₆-alkoxy-C₁-C₆-alkyl, NR^aR^b, phenyl, C₁-C₆-alkylphenyl;
  - R^a, R^bindependently of one another are hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₆-cycloalkyl or C₄-C₆-cycloalkenyl;
  - where the groups R^α may be substituted by one to four groups R^β:
  - R^βis halogen, cyano, hydroxyl, mercapto, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl and C₁-C₆-alkoxy;
    
    R¹and R²together with the carbon atoms to which they are attached may form a five- to seven-membered ring which may contain one to three identical or different heteroatoms from the group consisting of O, N and S;
R³is hydrogen, halogen, cyano, hydroxyl, mercapto, azido, C₁-C₈-alkyl, C₂-C₈-alkenyl, C₂-C₈-alkynyl, C₁-C₆-haloalkyl, —O-D, —S(O)_m-D, —ON═CR^aR^b, —CR^c═NOR^a, —NR^cN═CR^aR^b, —NR^aR^b, —NR^cNR^aR^b, —NOR^a, —NR^cC(═NR^c′)NR^aR^b, —NR^cC(═O)NR^aR^b, —NR^aCN, NR^aC(═O)R^c, —NR^aC(═NOR^c)R^c′, —OC(═O)R^a, —C(═NOR^c)NR^aR^b, —CR^c(═NNR^aR^b), —C(═O)NR^aR^b, —C(═O)R^a, —CO₂R^a, —C(═O)NR^zR^b, —C(═O)—N—OR^b, —C(═S)—NR^zR^b, —C(═NOR^a)NR^zR^b, —C(═NR^a)NR^zR^b, —C(═O)NR^a—NR^zR^b, —C(═N—NR^zR^c)NR^aR^b, —C(═NOR^b)R^a, C(═N—NR^zR^b)R^aCR^aR^b—OR^z, —CR^aR^b—NR^zR^c, —ON(═CR^aR^b), —NR^a(C(═)R^b), —NR^a(C(═O)OR^b), —NR^a(C(═O)—NR^zR^b), —NR^a(C(═NR^c)R^b), —NR^a(N═CR^cR^b), NR^a—NR^zR^b, —NR^z—OR^a, —NR^a(C(═NR^c)—NR^zR^b), —NR^a(C(═NOR^c)R^b),
- D is C₁-C₈-alkyl, C₃-C₈-alkenyl, C₃-C₈-alkynyl, C₁-C₆-haloalkyl, C₃-C₈-cycloalkyl;
- m is 0, 1 or 2;
- R^zis a group R^awhich may be attached directly or via a carbonyl group;
- R^cis one of the groups mentioned under R^a, R^b;
- a five- or six-membered saturated, partially unsaturated or aromatic mono- or bi-cyclic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S,
- one of the groups G1 or G2

- where
- x is 0 or 1;
- R^a, R^bare as defined above and, in group G1, together with the nitrogen atom to which they are attached may additionally have the meaning R^c-Z-C(R^d)═N;
- R^dis halogen, cyano, one of the groups mentioned under R^a, R^bor, together with the carbon to which it is attached, may be a carbonyl group;
  - Z is oxygen or N—R^c;
  - Y is C(H)—R^e, C—R^e, N—N(H)—R^cor N—R^c;
  - R^eis halogen, cyano or one of the groups mentioned under R^a, R^b;
- is a double or a single bond;
- where the aliphatic, alicyclic or aromatic groups R³, R^a, R^b, R^c, R^dor R^emay be partially or fully halogenated or may carry one to four groups R^A:
- R^Ais halogen, cyano, C₁-C₈-alkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₁-C₆-alkoxy, C₂-C₁₀-alkenyloxy, C₂-C₁₀-alkynyloxy, OH, SH, two vicinal groups R^Amay be (═O) or (═S), C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl, C₃-C₆-cycloalkoxy, C₃-C₆-cycloalkenyloxy, —C(═O)-A, —C(═O)—O-A, —C(═O)—N(A′)A, C(A′)(═N—OA), N(A′)A, N(A′)—C(═O)-A, N(A″)—C(═O)—N(A′)A, S(═O)_m-A, S(═O)_m—O-A or S(═O)_m—N(A′)A,
  - A, A′, A″ independently of one another are hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, where the groups may be partially or fully halogenated or may be substituted by cyano or C₁-C₄-alkoxy, or A and A′ together with the atoms to which they are attached are a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S;
  - where the aliphatic, alicyclic or aromatic groups R^A, A, A′ and A″ for their part may be partially or fully halogenated or may carry one to three groups R^b,
    
    for controlling harmful fungi.

Moreover, the invention relates to novel 4-aminopyrimidines, to processes for preparing these compounds and to compositions comprising them.

EP-A 407 899 and EP-A 12 54 903 propose fungicidally and/or microbicidally active aminopyrimidines in a general manner. However, in many cases their activity against phytopathogenic harmful fungi is unsatisfactory. Based on this, it is an object of the present invention to provide compounds having improved activity and/or a wider activity spectrum.

We have found that this object is achieved by the compounds defined at the outset. Furthermore, we have found processes and intermediates for their preparation, compositions comprising them and methods for controlling harmful fungi using the compounds I.

The compounds of the formula I differ from those in the abovementioned publications by the specific embodiment of the substituents in positions 4, 5 and 6 of the pyrimidine ring.

Compared to the known fungicidal compounds, the compounds of the formula I are more effective against harmful fungi.

The novel compounds of the formula I can be obtained by different routes.

Advantageously, the compounds of the formula I are obtained by converting substituted β-ketoesters of the formula II with thiourea of the formula III to give 2-thio-4-hydroxy-pyrimidines of the formula IV. The variables in formulae II and IV are as defined formula I and the group R in formula II is C₁-C₄-alkyl; for practical reasons, preference is given here to methyl, ethyl or propyl.

The reaction of the substituted β-ketoesters of the formula II with thiourea of the formula III can be carried out in the presence or absence of solvents. It is advantageous to use solvents to which the starting materials are substantially inert and in which they are completely or partially soluble.

Suitable solvents are in particular alcohols, such as ethanol, propanols, butanols, glycols or glycol monoethers, diethylene glycols or their monoethers, aromatic hydrocarbons, such as toluene, benzene or mesitylene, amides, such as dimethylformamide, diethylformamide, dibutylformamide, N,N-dimethylacetamide, lower alkanoic acids, such as formic acid, acetic acid, propionic acid, or bases, such as alkali metal and alkaline earth metal hydroxides, alkali metal and alkaline earth metal oxides, alkali metal and alkaline earth metal hydrides, alkali metal amides, alkali metal and alkaline earth metal carbonates and also alkali metal bicarbonates, organometallic compounds, in particular alkali metal alkyls, alkylmagnesium halides and also alkali metal and alkaline earth metal alkoxides and dimethoxymagnesium, moreover organic bases, for example tertiary amines, such as trimethylamine, triethylamine, triisopropylethylamine, tributylamine and N-methylpiperidine, N-methylmorpholine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminopyridine, and also bicyclic amines and mixtures of these solvents with water.

Suitable catalysts are bases as mentioned above or acids such as sulfonic acids or mineral acids. With particular preference, the reaction is carried out in the absence of a solvent or in chlorobenzene, xylene, dimethyl sulfoxide or N-methylpyrrolidone.

Particularly preferred bases are tertiary amines, such as triisopropylamine, tributylamine, N-methylmorpholine or N-methylpiperidine. The temperatures are from 50 to 300° C., preferably from 50 to 180° C., if the reaction is carried out in solution [cf. EP-A 770 615; Adv. Het. Chem. 57 (1993), 81ff].

The bases are generally employed in catalytic amounts; however, they can also be employed in equimolar amounts, in excess or, if appropriate, as solvent.

The β-ketoesters of the formula II can be prepared as described in Organic Synthesis Coll. Vol. 1, p. 248, and/or they are commercially available.

Using alkylating agents D-X, such as alkyl halides, preferably methyl chloride or methyl bromide, or dimethyl sulfate or methyl methanesulfonate, the 2-thio-4-hydroxypyrimidines of the formula IV are converted into the thioethers V. The reaction can be carried out in water or else in a dipolar aprotic solvent, such as, for example, N,N-dimethylformamide [cf. U.S. Pat. No. 5,250,689], it is advantageously carried out in the presence of a base, such as, for example, KOH, NaOH, NaHCO₃and Na₂CO₃or pyridine. The reaction temperature is preferably 10-60° C.

In the formulae V and VI, D is as defined in formula I.

Using halogenating agents, in particular chlorinating agents or brominating agents, the compounds of the formula V are converted into compounds of the formula VI in which Hal is chlorine or bromine, in particular chlorine. Suitable chlorinating agents for the conversion of the hydroxyl compounds V into the compounds VI are, for example, POCl₃, PCl₃/Cl₂or PCl₅, or mixtures of these reagents. The reaction can be carried out in excess chlorinating agent (POCl₃) or in an inert solvent, such as, for example, acetonitrile, toluene, chlorobenzene or 1,2-dichloroethane. The reaction is preferably carried out in POCl₃.

This reaction is usually carried out between 10 and 180° C. For practical reasons, the reaction temperature usually corresponds to the boiling point of the chlorinating agent (POCl₃) or solvent employed. The process is advantageously carried out with addition of catalytic or substoichiometric amounts of N,N-dimethylformamide or nitrogen bases, such as, for example, N,N-dimethylaniline.

Using ammonia in inert solvents, the halogenation product VI is then, at 100° C. to 200° C., converted into the 4-aminopyrimidines I in which R³is a group S-D (formula I.1). The reaction is preferably carried out using a 1- to 10-molar excess of ammonia under a pressure of from 1 to 100 bar.

Thioethers I.1 in which R³is a group S-D can be oxidized to give the corresponding sulfoxides or sulfones I.1. The oxidation is preferably carried out at from 10 to 50° C. in the presence of protic or aproptic solvents [cf.: B. Kor. Chem. Soc., Vol. 16, pp. 489-492 (1995); Z. Chem., Vol. 17, p. 63 (1977)]. Suitable oxidizing agents are, for example, hydrogen peroxide or 3-chloroperbenzoic acid. Hydrogen peroxide and peracids of organic carboxylic acids have been found to be particularly suitable oxidizing agents. The oxidation can also be carried out using selenium dioxide [cf.: ref. WO 02/88127].

The compounds of the formula I.2 are useful intermediates for preparing further compounds I. For practical reasons, particular preference is given to compounds I.2 in which D is C₁-C₄-alkyl, in particular methyl. In formula I.2, the substituents R¹and R²are as defined in formula I.

For preparing compounds of the formula I in which R³is cyano or a group attached via a heteroatom, hydroxyl, mercapto, azido, alkoxy, alkenyloxy, alkynyloxy, haloalkoxy, alkylthio, alkenylthio, alkynylthio, haloalkylthio, —ON═CR^aR^b, —NR^aN═CR^aR^b, NR^aR^b, —NR^aNR^aR^bor —NOR^a, it is advantageous to use sulfones of the formula I.2 as starting materials.

The sulfones of the formula I.2 are reacted with compounds of the formula VII under basic conditions. For practical reasons, it is alternatively possible to employ directly the alkali metal, alkaline earth metal or ammonium salt of the compound VII.

In the case of sufficiently nucleophilic reagents, this reaction is carried out under the conditions of nucleophilic substitution, usually at from 0 to 200° C., preferably from 10 to 150° C. in the presence of a dipolar aprotic solvent, such as N,N-dimethylformamide, tetrahydrofuran or acetonitrile [cf. DE-A 39 01 084; Chimia, Vol. 50, pp. 525-530 (1996); Khim. Geterotsikl. Soedin, Vol. 12, pp. 1696-1697 (1998)].

In general, the components are employed in approximately stoichiometric amounts. However, it may be advantageous to use an excess of the nucleophile of the formula R³—H.

In general, the reaction is carried out in the presence of a base which may be employed in equimolar amounts or else in excess. Suitable bases are alkali metal carbonates and bicarbonates, for example Na₂CO₃and NaHCO₃, nitrogen bases, such as triethylamine, tributylamine and pyridine, alkali metal alkoxides, such as sodium ethoxide or potassium tert-butoxide, alkali metal amides, such as NaNH₂, or else alkali metal hydrides, such as LiH or NaH.

Suitable solvents are halogenated hydrocarbons, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, 1,2-dimethoxyethane, dioxane, anisole and tetrahydrofuran, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide. Particular preference is given to ethanol, dichloromethane, acetonitrile and tetrahydrofuran. It is also possible to use mixtures of the solvents mentioned.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate. The bases are generally employed in catalytic amounts; however, they can also be used in excess.

The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an up to 10-fold, in particular up to 3-fold, excess of VII, based on I.2.

The compounds I in which R³is cyano (formula I.3) are useful intermediates for preparing further compounds I.

Compounds of the formula I in which R³is hydrogen, alkyl, alkenyl, alkynyl or haloalkyl are advantageously obtained from β-ketoesters of the formula II by reaction with amidines of the formula IIIa.

If, as amidine component IIIa, guanidine (R³═NH₂) is reacted with the β-ketoester II, 2-aminopyrimidines are obtained. Using generally customary alkylation and acylation processes, it is thus possible to synthesize, in a simple manner, pyrimidines according to the invention having, in the 2-position, a radical attached via nitrogen.

Analogously to the reaction sequence described above, the compounds Va are initially halogenated to give the 4-halopyrimidines VIa, which compounds VIa are reacted with ammonia under the conditions described for the compounds VI to give the corresponding compounds of the formula I.

An advantageous route for preparing the pyrimidines I in which R³is a group attached via nitrogen uses β-ketoesters II as starting materials. Reaction with urea IIIb gives the compounds Vb which can be halogenated, preferably chlorinated, to give VIb.

Using halogenating agents, in particular chlorinating agents or brominating agents, hydroxypyrimidines of the formula Vb are converted into halogen compounds of the formula VIb in which Hal is chlorine or bromine, in particular chlorine. Suitable chlorinating agents are, for example, POCl₃, PCl₃/Cl₂or PCl₅, or mixtures of these reagents. The reaction can be carried out in excess chlorinating agent (POCl₃) or in an inert solvent, such as, for example, acetonitrile, toluene, chlorobenzene or 1,2-dichloroethane. Preference is given to carrying out the reaction in POCl₃[cf. J. Chem. Soc. (1943) p. 383; Helv. Chim. Acta (1981) Vol. 64, pp. 113-152].

By reaction with ammonia, VIb gives 2,4-diaminopyrimidines of the formula I in which R³is NH₂.

This reaction is usually carried out using ammonia in inerten solvents at from 100° C. to 200° C. The reaction is preferably carried out using a 1- to 10-molar excess of ammonia under a pressure of from 1 to 100 bar.

Using generally known alkylation or acylation methods, the 2-amino group in formula I can be converted into other groups R³which are attached via nitrogen. Preferred alkylating or acylating agents are the alkylating agents D-X, such as dialkyl sulfate, alkyl halides, carbonyl chlorides, carboxylic anhydrides [cf.: Chem. Ber. Vol. 87, p. 1769 (1954)]

In the case of strong nucleophiles R³—H of the formula VII, the introduction of the substituent R³into the nitrile of the formula I.3 is carried out under the conditions of nucleophilic substitution. Moreover, the introduction can also be carried out under transition metal catalysis, such as, for example, under the Suzuki coupling reaction conditions. This reaction is advantageously carried out under the conditions known from J. Chem. Soc. (1943) p. 388 and J. Org. Chem. (1952) Vol. 17, p. 1320.

Alternatively, compounds of the formula I can be obtained by reacting substituted acyl cyanides of the formula VIII in which R¹and R²are as defined for formula I with thiourea of the formula III.

The reaction can be carried out in the presence or absence of solvents. It is advantageous to use solvents which are substantially inert toward the reactants and in which the reactants are completely or partially soluble. Suitable solvents are in particular alcohols, such as ethanol, propanols, butanols, glycols or glycol monoethers, diethylene glycols or monoethers thereof, aromatic hydrocarbons, such as toluene, benzene or mesitylene, amides, such as dimethylformamide, diethylformamide, dibutylformamide, N,N-dimethylacetamide, lower alkanoic acids, such as formic acid, acetic acid, propionic acid, or bases, as mentioned above, and mixtures of these solvents with water. The reaction temperatures are between 50 and 300° C., preferably from 50 to 150° C., if the reaction is carried out in solution.

Some of the substituted alkyl cyanides of the formula VIII required for preparing the compounds I are known, or they can be prepared by known methods from alkyl cyanides and carboxylic acid esters using strong bases, for example alkali metal hydrides, alkali metal alkoxides, alkali metal amides or metal alkyls (cf.: J. Amer. Chem. Soc. Vol. 73, (1951), p. 3766).

The further conversion of these thio compounds via alkylation and oxidation to give sulfoxides and sulfones which can be reated further with compounds R³—H of the formula VII has already been described further above.

Alternatively, compounds of the formula I in which R³is NR^aCN can also be prepared from 5,6-dialkyl-7-aminotriazolopyrimidines of the formula IX which are reacted under basic conditions with alkylating agents of the formula VIIa.

In formula VIIIa, X is a nucleophilically exchangeable group, such as a halogen atom, in particular an iodine atom. The reaction of VIIa with IX is usually carried out at temperatures of from −78° C. to 100° C., preferably from 10° C. to 80° C., in an inert organic solvent in the presence of a base [cf. WO 01/96314].

Compounds of the formula IX are known in a general manner from EP-A 141 317.

Compounds of the formula I in which R³is a derivatized carboxylic acid group, such as C(═O)R^c, —C(═O)NR^aR^b, —C(═NOR^c)NR^aR^b, —C(═NNR^aR^b)R^cor —C(═NOR^a)R^c, are advantageously obtained from compounds of the formula I.3.

Compounds of the formula I in which R³is —C(═O)NR^aR^bor —C(═NOR^c)NR^aR^bare obtainable from compounds of the formula I.3 by hydrolysis under acidic or basic conditions, to give the carboxylic acids of the formula I (where R³═COOH), and amidation with amines HNR^aR^b. The hydrolysis is usually carried out in inert polar solvents, such as water or alcohols, preferably using inorganic bases, such as alkali metal or alkaline earth metal hydroxides, in particular NaOH.

These reactions are advantageously carried out under the conditions known from Chem. and Pharm. Bull. 1982, Vol. 30, N12, p. 4314.

Amides of the formula I (where R³═CONH₂) afford, by oximation with substituted hydroxylamines H₂N—OR^cunder basic conditions, the compounds of the formula I in which R³is —C(═NOR^c)NR^aR^b[cf. U.S. Pat. No. 4,876,252]. The substituted hydroxylamines can be employed as free base or, preferably, in the form of their acid addition salts. For practical reasons, the halides, such as the chlorides or the sulfates, are particularly suitable.

Alternatively, the amidoximes of the formula I in which R³is —C(═NOR^c)NH₂can also be obtained form the corresponding nitriles of the formula I.3 by reaction with hydroxylamine and subsequent alkylation. This reaction is advantageously carried out under the conditions known from DE-A 198 37 794.

Compounds of the formula I in which R³is —C(═O)R^ccan be obtained from the corresponding nitriles of the formula I.3 by reaction with Grignard reagents R^c—Mg-Hal, where Hal is a halogen atom, in particular chlorine or bromine.

This reaction is advantageously carried out under the conditions known from J. Heterocycl. Chem. 1994, Vol. 31(4), p. 1041.

Compounds of the formula I in which R³is —C(═NNR^aR^b)R^ccan be obtained via compounds I (where R³═C(O)R^c) which are reacted with hydrazines H₂NNR^aR^b, preferably under the conditions known from J. Org. Chem. 1966, Vol. 31, p. 677.

Compounds of the formula I in which R³is —C(═NOR^a)R^ccan be obtained via oximation of compounds I (where R³═C(O)R^c). The oximation is carried out as described above.

Compounds of the formula I in which R¹is C₁-C₁₄-haloalkyl, C₁-C₁₂-haloalkoxy-C₁-C₁₂-alkyl, C₁-C₁₂-alkoxy-C₁-C₁₂-haloalkyl, C₂-C₁₂-haloalkenyl or C₂-C₁₂-haloalkynyl can be obtained by halogenation of corresponding halogen-free pyrimidines of the formula I, they are referred to as compounds I′. In formula I′, R^1′ is a halogen-free group R¹. In formula I″, R^1″is a halogenated group R¹:

The halogenation is usually carried out at temperatures of from 0° C. to 200° C., preferably from 20° C. to 110° C., in an inert organic solvent in the presence of a free-radical initiator (for example dibenzoyl peroxide or azobisisobutyronitrile or under UV irradiation using, for example, an Hg vapor lamp) or an acid [cf. Synthetic Reagents, Vol. 2, pp. 1-63, Wiley Publishers, New York (1974)].

The reaction partners are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of halogenating agent, based on I′.

Suitable halogenating agents are, for example, elemental halogens (for example Cl₂, Br₂, I₂), N-bromosuccinimide, N-chlorosuccinimide oder dibromodimethylhydrantoin. The halogenating agents are generally employed in equimolar amounts, in excess or, if appropriate, as solvent.

The reaction mixtures are worked up in a customary manner, for example by mixing with water, separating the phases and, if appropriate, chromatographic purification of the crude products. Some of the intermediates and end products are obtained in the form of colorless or slightly brownish viscous oils which can be purified or freed from volatile components under reduced pressure and at moderately elevated temperature. If the intermediates and end products are obtained as solids, purification can also be carried out by recrystallization or digestion.

If individual compounds I cannot be obtained by the routes described above, they can be prepared by derivatization of other compounds I.

If the synthesis yields mixtures of isomers, a separation is generally not necessarily required, however, since in some cases the individual isomers can be interconverted during work-up for use or during application (for example under the action of light, acids or bases). Such conversions may also take place after use, for example in the treatment of plants in the treated plants, or in the harmful fungus to be controlled.

In the definitions of symbols given in the formulae above, collective terms were used which are generally representative of the following substituents:

halogen: fluorine, chlorine, bromine and iodine;

alkyl: saturated straight-chain or branched hydrocarbon radicals having 1 to 4, 6, 8 or 10 carbon atoms, for example C₁-C₆-alkyl such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl;

haloalkyl: straight-chain or branched alkyl groups having 1 to 2, 4 or 6 carbon atoms (as mentioned above), where in these groups some or all of the hydrogen atoms may be replaced by halogen atoms as mentioned above: in particular C₁-C₂-haloalkyl, such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl or 1,1,1-trifluoroprop-2-yl;

alkenyl: unsaturated straight-chain or branched hydrocarbon radicals having 2 to 4, 6, 8 or 10 carbon atoms and one or two double bonds in any position, for example C₂-C₆-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl and 1-ethyl-2-methyl-2-propenyl;

haloalkenyl: unsaturated straight-chain or branched hydrocarbon radicals having 2 to 10 carbon atoms and one or two double bonds in any position (as mentioned above), where in these groups some or all of the hydrogen atoms may be replaced by halogen atoms as mentioned above, in particular by fluorine, chlorine and bromine;

alkynyl: straight-chain or branched hydrocarbon groups having 2 to 4, 6, 8 or 10 carbon atoms and one or two triple bonds in any position, for example C₂-C₆-alkynyl, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl and 1-ethyl-1-methyl-2-propynyl;

cycloalkyl: mono- or bicyclic saturated hydrocarbon groups having 3 to 6 or 8 carbon ring members, for example C₃-C₈-cycloalkyl such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl;

five- or six-membered saturated, partially unsaturated or aromatic heterocycle which contains one to four heteroatoms from the group consisting of O, N and S:

- 5- or 6-membered heterocyclyl which contains one to three nitrogen atoms and/or one oxygen or sulfur atom or one or two oxygen and/or sulfur atoms, for example 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazolidinyl, 4-isoxazolidinyl, 5-isoxazolidinyl, 3-isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazolidinyl, 3-pyrazolidinyl, 4-pyrazolidinyl, 5-pyrazolidinyl, 2-oxazolidinyl, 4-oxazolidinyl, 5-oxazolidinyl, 2-thiazolidinyl, 4-thiazolidinyl, 5-thiazolidinyl, 2-imidazolidinyl, 4-imidazolidinyl, 2-pyrrolin-2-yl, 2-pyrrolin-3-yl, 3-pyrrolin-2-yl, 3-pyrrolin-3-yl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 1,3-dioxan-5-yl, 2-tetrahydropyranyl, 4-tetrahydropyranyl, 2-tetrahydrothienyl, 3-hexahydropyridazinyl, 4-hexahydropyridazinyl, 2-hexahydropyrimidinyl, 4-hexahydropyrimidinyl, 5-hexahydropyrimidinyl and 2-piperazinyl;
- 5-membered heteroaryl which contains one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom: 5-membered heteroaryl groups which, in addition to carbon atoms, may contain one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom as ring members, for example 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-imidazolyl, 4-imidazolyl and 1,3,4-triazol-2-yl;
- 6-membered heteroaryl which contains one to three or one to four nitrogen atoms: 6-membered heteroaryl groups which, in addition to carbon atoms, may contain one to three and one to four nitrogen atoms, respectively, as ring members, for example 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, 3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 2-pyrazinyl;
  
  alkylene: divalent unbranched chains of 1 to 5 CH₂groups, for example CH₂, CH₂CH₂, CH₂CH₂CH₂, CH₂CH₂CH₂CH₂and CH₂CH₂CH₂CH₂CH₂;
  
  oxyalkylene: divalent unbranched chains of 2 to 4 CH₂groups, where one valency is attached to the skeleton via an oxygen atom, for example OCH₂CH₂, OCH₂CH₂CH₂and OCH₂CH₂CH₂CH₂;
  
  oxyalkyleneoxy: divalent unbranched chains of 1 to 3 CH₂groups, where both valencies are attached to the skeleton via an oxygen atom, for example OCH₂O, OCH₂CH₂O and OCH₂CH₂CH₂O.

The scope of the present invention includes the (R) and (S) isomers and the racemates of compounds of the formula I having chiral centers.

With respect to the variables, the particularly preferred embodiments of the intermediates correspond to those of the formula I.

With a view to the intended use of the 4-aminopyrimidines of the formula I, particular preference is given to the following meanings of the substituents, in each case on their own or in combination:

Preference is given to compounds I in which the group R¹has at most 9 carbon atoms. Preference is likewise given to compounds of the formula I in which the groups R¹and R²together have at most 14 carbon atoms.

In one embodiment of the compounds I according to the invention, R¹and R²independently of one another are halogen, cyano, C₁-C₁₂-alkyl, C₁-C₁₂-haloalkyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl, C₃-C₈-cycloalkyl, C₁-C₁₂-alkoxy, C₁-C₆-alkoxy-C₁-C₆-alkyl, where the carbon chains in R¹and/or R²may be substituted by one to four identical or different of the groups R^abelow:

- halogen, cyano, C₁-C₁₀-alkyl, C₁-C₁₀-haloalkyl, C₃-C₈-cycloalkyl, C₂-C₁₀-alkenyl, C₂-C₁₀-alkynyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, phenyl which may be substituted by an alkyl group.

In a preferred embodiment of the compounds I according to the invention, R¹and R²independently of one another are C₁-C₁₂-alkyl, C₁-C₁₂-haloalkyl, C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl, C₃-C₈-cycloalkyl, C₁-C₁₂-alkoxy, C₁-C₆-alkoxy-C₁-C₆-alkyl, where the carbon chains in R¹and/or R²may be substituted as described above.

Particular preference is given to those compounds I in which R²is C₁-C₅-alkyl, C₁-C₅-haloalkyl, C₂-C₅-alkenyl, C₂-C₅-alkynyl, C₃-C₅-cycloalkyl, C₁-C₅-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl, which groups are unsubstituted or substituted by halogen, cyano, methyl or ethyl.

In a further preferred embodiment of the compounds I according to the invention, R²is C₁-C₅-alkyl, C₁-C₅-haloalkyl, C₂-C₅-alkenyl, C₂-C₅-alkynyl, C₃-C₅-cycloalkyl, C₁-C₅-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl, which groups are unsubstituted or substituted by halogen, cyano, methyl or ethyl.

In a further particularly preferred embodiment of the compounds I according to the invention,

R¹is C₁-C₁₂-alkyl, C₁-C₁₂-haloalkyl, C₂-C₁₂-alkenyl, C₃-C₁₂-alkynyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, and
R²is C₁-C₅-alkyl, C₁-C₅-haloalkyl, C₂-C₅-alkenyl, C₂-C₅-alkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,

where the carbon chains in R¹and/or R²may be partially or fully halogenated or substituted by C₂-C₅-alkenyl or C₂-C₅-alkynyl.

In a further particularly preferred embodiment of the compounds I according to the invention, R²is C₁-C₅-alkyl, C₁-C₅-haloalkyl, C₂-C₅-alkenyl, C₂-C₅-alkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, where the carbon chains in R¹and/or R²may be partially or fully halogenated.

In a preferred embodiment of the compounds of the formula I, group R¹is absent.

In one embodiment of the compounds I according to the invention, R²is methyl, ethyl, isopropyl, n-propyl or n-butyl, in particular methyl.

Halogen atoms in the groups R¹and/or R²are preferably located at the α or at the terminal carbon atom.

Cyano groups in R¹and/or R²are preferably located at the terminal carbon atom.

In a further preferred embodiment of the compounds of the formula I, group R^bis absent.

In a further preferred embodiment of the compounds I according to the invention, R³is halogen, cyano, hydroxyl, mercapto, amino, C₂-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₈-cycloalkyl, C₁-C₆-alkoxy or C₁-C₆-alkylthio.

Particular preference is likewise given to compounds I in which R³is hydrogen, cyano, azido, C₁-C₆-alkyl, C₂-C₈-alkenyl, C₂-C₈-alkynyl, C₁-C₆-haloalkyl, or —ON═CR^aR^bor —NR^cN═CR^aR^bor —C(═NOR^c)NR^aR^b.

Especially preferred are compounds I in which R³is cyano, —CR^aNOR^bor —ON═CR^aR^b, in particular —ON═CR^aR^b.

In addition, preference is given to compounds I in which R³is —NH(═NH)NHR^c, —NHC(═O)NHR^a, —NHC(═O)R^a, —OC(═O)R^a, —C(═NOR^c)NH₂or —CR^c(═NNR^aR^b).

Preference is furthermore given to compounds I in which R³is —NR^cN═CR^aR^b.

Preference is likewise given to compounds I in which R³is —C(═NOR^c)NR^aR^b, in particular —C(═NOR^c)NH₂.

In addition, particular preference is given to compounds I in which R³is an aromatic five-membered heterocycle which is preferably attached via N and/or may be substituted by one or two groups R^A.

Preference is furthermore given to pyrimidines of the formula I in which R³is cyano, CO₂R^a, C(═O)NR^zR^b, C(═NOR^a)NR^zR^b, C(═NR^a)NR^zR^b, C(═O)NR^a—NR^zR^b, C(═N—NR^zR^c)NR^aR^b, C(═O)R^a, C(═NOR^b)R^a, C(═O)—N(R^a)—OR^b, C(═S)—NR^aR^b, C(═N—NR^zR^b)R^a, CR^aR^b—OR^zor CR^aR^b—NR^zR^c.

Especially preferred are pyrimidines of the formula I in which R³is cyano, C(═O)NR^zR^b, C(═O)—N(R^a)—OR^b, C(═S)—NR^aR^b, C(═NOR^a)NR^zR^b, C(═NOR^b)R^a, C(═N—NR^zR^b)R^aor CR^aR^b—NR^zR^c.

Moreover, preference is given to pyrimidines of the formula I in which R³is ON(═CR^aR^b) or O—C(═O)R^a.

Preference is furthermore given to pyrimidines of the formula I in which R³is NR^aR^b′, NR^a(C(═O)R^b), NR^a(C(═O)OR^b), NR^a(C(═O)—NR^zR^b), NR^a(C(═NR^c)R^b), NR^a(N═CR^cR^b), NR^a—NR^zR^b, NR^z—OR^a, NR^a(C(═NR^c)—NR^zR^b), NR^a(C(═NOR^c)R^b).

Especially preferred are pyrimidines of the formula I in which R³is NR^a(C(═O)R^b), NR^a(C(═O)OR^b), NR^a(N═CR^cR^b), NR^z—OR^a.

R^a, R^band R^care preferably independently of one another hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl or C₃-C₆-cycloalkyl.

R^zhas preferably the abovementioned preferred meanings of R^a, R^band R^c. Particularly preferred is the meaning —CO—R^a.

Especially preferred are the following groups of compounds of the formula I:

If compounds I.1 and I.2 are used as intermediates, D is in particular C₁-C₄-alkyl, preferably methyl.

Compounds of the formulae I.34 and I.35 are also useful intermediates for preparing other compounds I. In the formulae I.34 and I.35, R is C₁-C₄-alkyl, in particular methyl, and R^Aand R^A′are in particular methyl.

In particular with a view to their use, preference is given to the compounds I compiled in the tables below. Moreover, the groups mentioned for a substituent in the tables are per se, independently of the combination in which they are mentioned, a particularly preferred embodiment of the substituent in question.

Table 1

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is methyl

Table 2

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is methyl

Table 3

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 4

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 5

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 6

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 7

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 8

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 9

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 10

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 11

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 12

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 13

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A and R²and R are methyl

Table 14

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is methyl and R is ethyl

Table 15

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is methyl and R is n-propyl

Table 16

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is methyl and R is isopropyl

Table 17

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 18

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 19

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 20

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 21

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 22

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 23

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 24

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 25

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 26

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 27

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 28

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 29

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 30

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 31

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 32

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 33

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 34

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 35

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 36

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 37

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A and R²and R are methyl

Table 38

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A and R, R², R^{A and R}^A′are methyl

Table 39

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 40

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is methyl

Table 41

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is methyl and R is hydrogen

Table 42

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A and R²and R are methyl

Table 43

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is ethyl

Table 44

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is ethyl

Table 45

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 46

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 47

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 48

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 49

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 50

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 51

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 52

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 53

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 54

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 55

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is ethyl and R is methyl

Table 56

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A and R²and R are ethyl

Table 57

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is ethyl and R is n-propyl

Table 58

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is ethyl and R is isopropyl

Table 59

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 60

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 61

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 62

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 63

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 64

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 65

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 66

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 67

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 68

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 69

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 70

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 71

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 72

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 73

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 74

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 75

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 76

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 77

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 78

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 79

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is ethyl and R is methyl

Table 80

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is ethyl and R, R^Aand R^A′are methyl

Table 81

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 82

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is ethyl

Table 83

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is ethyl and R is hydrogen

Table 84

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is ethyl and R is methyl

Table 85

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-propyl

Table 86

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-propyl

Table 87

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 88

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 89

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 90

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 91

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 92

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 93

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 94

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 95

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 96

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 97

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-propyl and R is methyl

Table 98

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-propyl and R is ethyl

Table 99

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A and R²and R are n-propyl

Table 100

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-propyl and R is isopropyl

Table 101

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 102

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 103

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 104

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 105

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 106

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 107

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 108

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 109

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 110

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 111

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 112

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 113

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 114

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 115

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 116

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 117

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 118

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 119

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 120

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 121

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is n-propyl and R is methyl

Table 122

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is n-propyl and R, R^Aand R^A′are methyl

Table 123

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 124

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is n-propyl

Table 125

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-propyl and R is hydrogen

Table 126

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-propyl and R is methyl

Table 127

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is isopropyl

Table 128

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is isopropyl

Table 129

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 130

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 131

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 132

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 133

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 134

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 135

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 136

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 137

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 138

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 139

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is isopropyl and R is methyl

Table 140

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is isopropyl and R is ethyl

Table 141

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is isopropyl and R is n-propyl

Table 142

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A and R²and R are isopropyl

Table 143

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 144

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 145

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 146

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 147

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 148

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 149

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 150

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 151

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 152

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 153

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 154

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 155

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 156

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 157

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 158

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 159

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 160

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 161

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 162

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 163

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is isopropyl and R is methyl

Table 164

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is isopropyl and R, R^Aand R^A′are methyl

Table 165

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 166

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is isopropyl

Table 167

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is isopropyl and R is hydrogen

Table 168

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is isopropyl and R is methyl

Table 169

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-butyl

Table 170

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-butyl

Table 171

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 172

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 173

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 174

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 175

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 176

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 177

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 178

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 179

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 180

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 181

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-butyl and R is methyl

Table 182

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-butyl and R is ethyl

Table 183

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-butyl and R is n-propyl

Table 184

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-butyl and R is isopropyl

Table 185

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 186

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 187

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 188

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 189

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 190

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 191

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 192

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 193

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 194

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 195

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 196

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 197

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 198

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 199

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 200

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 201

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 202

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 203

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 204

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 205

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is n-butyl and R is methyl

Table 206

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is n-butyl and R, R^Aand R^A′ are methyl

Table 207

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 208

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is n-butyl

Table 209

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-butyl and R is hydrogen

Table 210

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-butyl and R is methyl

Table 211

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-pentyl

Table 212

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-pentyl

Table 213

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 214

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 215

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 216

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 217

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 218

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 219

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 220

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 221

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 222

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 223

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-pentyl and R is methyl

Table 224

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-pentyl and R is ethyl

Table 225

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-pentyl and R is n-propyl

Table 226

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-pentyl and R is isopropyl

Table 227

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 228

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 229

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 230

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 231

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 232

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 233

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 234

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 235

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 236

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 237

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 238

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 239

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 240

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 241

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 242

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 243

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 244

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 245

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 246

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 247

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is n-pentyl and R is methyl

Table 248

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is n-pentyl and R, R^Aand R^A′are methyl

Table 249

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 250

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is n-pentyl

Table 251

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-pentyl and R is hydrogen

Table 252

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-pentyl and R is methyl

Table 253

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-hexyl

Table 254

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-hexyl

Table 255

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 256

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 257

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 258

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 259

Compounds of the formula I.7 in which R¹for each compounds corresponds to one row of Table A and R²is n-hexyl

Table 260

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 261

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 262

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 263

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 264

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 265

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-hexyl and R is methyl

Table 266

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-hexyl and R is ethyl

Table 267

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-hexyl and R is n-propyl

Table 268

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-hexyl and R is isopropyl

Table 269

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 270

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 271

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 272

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 273

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 274

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 275

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 276

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 277

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 278

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 279

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 280

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 281

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 282

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 283

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 284

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 285

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 286

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 287

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl.

Table 288

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 289

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is n-hexyl and R is methyl

Table 290

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is n-hexyl and R, R^Aand R^A′are methyl

Table 291

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 292

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is n-hexyl

Table 293

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-hexyl and R is hydrogen

Table 294

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-hexyl and R is methyl

Table 295

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-heptyl

Table 296

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-heptyl

Table 297

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 298

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 299

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 300

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 301

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 302

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 303

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 304

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 305

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 306

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 307

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-heptyl and R is methyl

Table 308

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-heptyl and R is ethyl

Table 309

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-heptyl and R is n-propyl

Table 310

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-heptyl and R is isopropyl

Table 311

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 312

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 313

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 314

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 315

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 316

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 317

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 318

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 319

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 320

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 321

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl.

Table 322

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 323

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 324

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 325

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 326

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 327

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 328

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 329

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 330

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 331

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is n-heptyl and R is methyl

Table 332

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is n-heptyl and R, R^Aand R^A′are methyl

Table 333

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 334

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is n-heptyl

Table 335

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-heptyl and R is hydrogen

Table 336

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-heptyl and R is methyl

Table 337

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-octyl

Table 338

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-octyl

Table 339

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 340

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 341

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 342

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 343

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 344

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 345

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 346

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 347

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 348

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 349

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-octyl and R is methyl

Table 350

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-octyl and R is ethyl

Table 351

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-octyl and R is n-propyl

Table 352

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-octyl and R is isopropyl

Table 353

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 354

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 355

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 356

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 357

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 358

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 359

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 360

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 361

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 362

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 363

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 364

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 365

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 366

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 367

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 368

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 369

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 370

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 371

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 372

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 373

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is n-octyl and R is methyl

Table 374

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is n-octyl and R, R^Aand R^A′are methyl

Table 375

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 376

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is n-octyl

Table 377

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-octyl and R is hydrogen

Table 378

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-octyl and R is methyl

Table 379

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-nonyl

Table 380

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-nonyl

Table 381

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 382

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 383

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 384

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 385

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 386

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 387

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 388

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 389

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 390

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 391

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-nonyl and R is methyl

Table 392

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-nonyl and R is ethyl

Table 393

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-nonyl and R is n-propyl

Table 394

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-nonyl and R is isopropyl

Table 395

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 396

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 397

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 398

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 399

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 400

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 401

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 402

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 403

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²n-nonyl

Table 404

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 405

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 406

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 407

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 408

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 409

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 410

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 411

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 412

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 413

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 414

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 415

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is n-nonyl and R is methyl

Table 416

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is n-nonyl and R, R^Aand R^A′are methyl

Table 417

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 418

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is n-nonyl

Table 419

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-nonyl and R is hydrogen

Table 420

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-nonyl and R is methyl

Table 421

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-decyl

Table 422

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is n-decyl

Table 423

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 424

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 425

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 426

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 427

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 428

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 429

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 430

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 431

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 432

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 433

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-decyl and R is methyl

Table 434

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-decyl and R is ethyl

Table 435

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-decyl and R is n-propyl

Table 436

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is n-decyl and R is isopropyl

Table 437

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 438

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 439

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 440

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 441

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 442

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 443

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 444

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 445

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 446

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 447

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 448

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 449

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 450

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 451

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 452

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 453

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 454

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 455

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 456

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 457

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is n-decyl and R is methyl

Table 458

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is n-decyl and R, R^Aand R^A′are methyl

Table 459

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 460

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is n-decyl

Table 461

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-decyl and R is hydrogen

Table 462

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is n-decyl and R is methyl

Table 463

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is methoxymethyl

Table 464

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is methoxymethyl

Table 465

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 466

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 467

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 468

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 469

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 470

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 471

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 472

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 473

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 474

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 475

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is methoxymethyl and R is methyl

Table 476

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is methoxymethyl and R is ethyl

Table 477

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is methoxymethyl and R is n-propyl

Table 478

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is methoxymethyl and R is isopropyl

Table 479

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 480

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 481

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 482

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 483

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 484

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 485

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 486

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 487

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 488

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 489

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 490

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 491

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 492

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 493

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 494

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 495

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 496

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 497

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 498

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 499

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is methoxymethyl and R is methyl

Table 500

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is methoxymethyl and R, R^Aand R^A′are methyl

Table 501

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 502

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is methoxymethyl

Table 503

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is methoxymethyl and R is hydrogen

Table 504

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is methoxymethyl and R is methyl

Table 505

Compounds of the formula I.1 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is ethoxymethyl

Table 506

Compounds of the formula I.2 in which R¹for each compound corresponds to one row of Table A, D is methyl and R²is ethoxymethyl

Table 507

Compounds of the formula I.3 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 508

Compounds of the formula I.4 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 509

Compounds of the formula I.5 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 510

Compounds of the formula I.6 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 511

Compounds of the formula I.7 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 512

Compounds of the formula I.8 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 513

Compounds of the formula I.9 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 514

Compounds of the formula I.10 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 515

Compounds of the formula I.11 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 516

Compounds of the formula I.12 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 517

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is ethoxymethyl and R is methyl

Table 518

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is ethoxymethyl and R is ethyl

Table 519

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is ethoxymethyl and R is n-propyl

Table 520

Compounds of the formula I.13 in which R¹for each compound corresponds to one row of Table A, R²is ethoxymethyl and R is isopropyl

Table 521

Compounds of the formula I.14 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 522

Compounds of the formula I.15 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 523

Compounds of the formula I.16 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 524

Compounds of the formula I.17 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 525

Compounds of the formula I.18 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 526

Compounds of the formula I.19 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 527

Compounds of the formula I.20 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 528

Compounds of the formula I.21 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 529

Compounds of the formula I.22 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 530

Compounds of the formula I.23 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 531

Compounds of the formula I.24 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 532

Compounds of the formula I.25 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 533

Compounds of the formula I.26 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 534

Compounds of the formula I.27 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 535

Compounds of the formula I.28 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 536

Compounds of the formula I.29 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 537

Compounds of the formula I.30 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 538

Compounds of the formula I.31 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 539

Compounds of the formula I.32 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 540

Compounds of the formula I.33 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 541

Compounds of the formula I.34 in which R¹for each compound corresponds to one row of Table A, R²is ethoxymethyl and R is methyl

Table 542

Compounds of the formula I.35 in which R¹for each compound corresponds to one row of Table A, R²is ethoxymethyl and R, R^Aand R^A′are methyl

Table 543

Compounds of the formula I.36 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 544

Compounds of the formula I.37 in which R¹for each compound corresponds to one row of Table A and R²is ethoxymethyl

Table 545

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is ethoxymethyl and R is hydrogen

Table 546

Compounds of the formula I.38 in which R¹for each compound corresponds to one row of Table A, R²is ethoxymethyl and R is methyl

TABLE A

No.
R¹

A-1
CH₃

A-2
CH₂CH₃

A-3
CH₂CH₂CH₃

A-4
CH(CH₃)₂

A-5
CH₂CH₂CH₂CH₃

A-6
CH(CH₃)CH₂CH₃

A-7
CH₂CH(CH₃)₂

A-8
C(CH₃)₃

A-9
CH₂CH₂CH₂CH₂CH₃

A-10
CH(CH₃)CH₂CH₂CH₃

A-11
CH₂CH(CH₃)CH₂CH₃

A-12
CH₂CH₂CH(CH₃)CH₃

A-13
CH₂CH₂CH(CH₃)₂

A-14
CH(CH₃)CH(CH₃)CH₃

A-15
CH(CH₃)CH(CH₃)₂

A-16
CH₂C(CH₃)₃

A-17
CH₂CH₂CH₂CH₂CH₂CH₃

A-18
CH(CH₃)CH₂CH₂CH₂CH₃

A-19
CH₂CH(CH₃)CH₂CH₂CH₃

A-20
CH₂CH₂CH(CH₃)CH₂CH₃

A-21
CH₂CH₂CH(CH₃)₂CH₂

A-22
CH₂CH₂CH₂CH(CH₃)₂

A-23
CH(CH₃)CH(CH₃)CH₂CH₃

A-24
CH(CH₃)CH₂CH(CH₃)₂

A-25
CH₂CH₂C(CH₃)₃

A-26
CH(CH₃)CH₂CH(CH₃)CH₃

A-27
CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-28
CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-29
CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-30
CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-31
CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-32
CH₂CH₂CH₂CH₂CH(CH₃)CH₃

A-33
CH₂CH₂CH₂CH₂CH(CH₃)₂

A-34
CH(CH₃)CH(CH₃)CH₂CH₂CH₃

A-35
CH₂CH(CH₃)CH(CH₃)CH₂CH₃

A-36
CH₂CH₂CH₂C(CH₃)₃

A-37
CH(CH₃)CH₂CH(CH₃)CH₂CH₃

A-38
CH₂CH(CH₃)CH(CH₃)CH₂CH₃

A-39
CH(CH₃)CH₂CH₂CH(CH₃)CH₃

A-40
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-41
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-42
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-43
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-44
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-45
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-46
CH₂CH₂CH₂CH₂CH₂CH(CH₃)₂

A-47
CH₂CH₂CH₂CH₂C(CH₃)₃

A-48
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₃

A-49
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₃

A-50
CH₂CH₂CH₂C(CH₃)₂CH₂CH₃

A-51
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₃

A-52
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₃

A-53
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₃

A-54
CH(CH₃)CH₂CH₂CH₂CH(CH₃)₂

A-55
CH₂CH₂CH(CH₃)CH₂C(CH₃)₃

A-56
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-57
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-58
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-59
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-60
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-61
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-62
CH₂CH₂CH₂CH₂CH₂CH₂C(CH₃)₃

A-63
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-64
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₃

A-65
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CH₃

A-66
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-67
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₃

A-68
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-69
CH(CH₃)CH₂CH₂CH₂C(CH₃)₃

A-70
CH₂CH(CH₃)CH₂CH₂CH(CH₃)₃

A-71
CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)₂

A-72
CH₂CH(CH₃)CH₂CH₂CH₂CH(CH₃)₂

A-73
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-74
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-75
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-76
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-77
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂

A-78
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-79
CH₂CH₂CH₂CH₂CH₂CH₂C(CH₃)₃

A-80
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-81
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-82
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CH₂CH₃

A-83
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-84
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-85
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-86
CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-87
CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-88
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH(CH₃)₂

A-89
CH(CH₃)CH₂CH₂CH₂CH₂CH₂C(CH₃)CH₃

A-90
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₃

A-91
CH(CH₃)CH₂CH₂CH₂CH₂C(CH₃)₃

A-92
CH₂CH(CH₃)CH₂CH₂CH₂C(CH₃)₃

A-93
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-94
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-95
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-96
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-97
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-98
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-99
CH₂CH₂CH₂CH₂CH₂CH₂CH₂C(CH₃)₃

A-100
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-101
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-102
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CH₂CH₂CH₃

A-103
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-104
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-105
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-106
CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-107
CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-108
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-109
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)₂

A-110
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-111
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-112
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)₂

A-113
CH₂CH(CH₃)CH₂CH₂CH₂CH₂C(CH₃)₃

A-114
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-115
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-116
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-117
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-118
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂

A-119
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-120
CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-121
CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-122
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-123
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-124
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)₂

A-125
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-126
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-127
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CH₂CH₂CH₂CH₃

A-128
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-129
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-130
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₃

A-131
CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₃

A-132
CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₃

A-133
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-134
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-135
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₃

A-136
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-137
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CH₃

A-138
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂C(CH₃)₃

A-139
CH₂CH₂CH₂—O—CH₃

A-140
CH₂CH₂CH₂—O—CH₂CH₃

A-141
CH₂CH₂CH₂—O—CH₂CH₂CH₃

A-142
CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₃

A-143
CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₃

A-144
CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₃

A-145
CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-146
CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-147
CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-148
CH₂CH₂CH₂—O—CH(CH₃)₂

A-149
CH₂CH₂CH₂—O—C(CH₃)₃

A-150
CH₂CH₂CH₂—O—CH₂C(CH₃)₃

A-151
CH₂CH₂CH₂—O—CH(CH₃)CH₂C(CH₃)₃

A-152
CH₂CH₂CH₂—O—CH(CH₂CH₃)CH₂C(CH₃)₃

A-153
CH₂CH₂CH₂—O—CH₂CH(CH₃)CH₂CH(CH₃)₂

A-154
CH₂CH₂CH₂—O—CH₂CH(CH₂CH₃)CH₂CH₂CH₃

A-155
CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂CH(CH₃)₂

A-156
CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂C(CH₃)₃

A-157
CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂CH₂CH(CH₃)₂

A-158
CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH(CH₃)₂

A-159
CH₂CH₂CH₂CH₂—O—CH₃

A-160
CH₂CH₂CH₂CH₂—O—CH₂CH₃

A-161
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₃

A-162
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₃

A-163
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₃

A-164
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₃

A-165
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-166
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-167
CH₂CH₂CH₂CH₂—O—CH(CH₃)₂

A-168
CH₂CH₂CH₂CH₂—O—C(CH₃)₃

A-169
CH₂CH₂CH₂CH₂—O—CH₂C(CH₃)₃

A-170
CH₂CH₂CH₂CH₂—O—CH(CH₃)CH₂C(CH₃)₃

A-171
CH₂CH₂CH₂CH₂—O—CH(CH₂CH₃)CH₂C(CH₃)₃

A-172
CH₂CH₂CH₂CH₂—O—CH₂CH(CH₃)CH₂CH(CH₃)₂

A-173
CH₂CH₂CH₂CH₂—O—CH₂CH(CH₂CH₃)CH₂CH₂CH₃

A-174
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂CH(CH₃)₂

A-175
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂C(CH₃)₃

A-176
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂CH₂CH(CH₃)₂

A-177
CH₂CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH(CH₃)₂

A-178
CH₂CH₂CH₂CH₂CH₂—O—CH₃

A-179
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₃

A-180
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₃

A-181
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₃

A-182
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₃

A-183
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₃

A-184
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-185
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-186
CH₂CH₂CH₂CH₂CH₂—O—CH(CH₃)₂

A-187
CH₂CH₂CH₂CH₂CH₂—O—C(CH₃)₃

A-188
CH₂CH₂CH₂CH₂CH₂—O—CH₂C(CH₃)₃

A-189
CH₂CH₂CH₂CH₂CH₂—O—CH(CH₃)CH₂C(CH₃)₃

A-190
CH₂CH₂CH₂CH₂CH₂—O—CH(CH₂CH₃)CH₂C(CH₃)₃

A-191
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH(CH₃)CH₂CH(CH₃)₂

A-192
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH(CH₂CH₃)CH₂CH₂CH₃

A-193
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂CH₂CH(CH₃)₂

A-194
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂CH(CH₃)₂

A-195
CH₂CH₂CH₂CH₂CH₂—O—CH₂CH₂CH(CH₃)CH₂C(CH₃)₃

A-196
CH₂F

A-197
CH₂Cl

A-198
CH₂Br

A-199
CHF₂

A-200
CHCl₂

A-201
CF₃

A-202
CCl₃

A-203
CHFCH₃

A-204
CHClCH₃

A-205
CH₂CH₂F

A-206
CH₂CH₂Cl

A-207
CH₂CH₂Br

A-208
CCl₂CH₃

A-209
CF₂CH₃

A-210
CH₂CHF₂

A-211
CH₂CHCl₂

A-212
CH₂CF₃

A-213
CH₂CCl₃

A-214
CF₂CF₃

A-215
CCl₂CCl₃

A-216
CHFCH₂CH₃

A-217
CHClCH₂CH₃

A-218
CH₂CHFCH₃

A-219
CH₂CHClCH₃

A-220
CH₂CH₂CH₂F

A-221
CH₂CH₂CH₂Cl

A-222
CH₂CH₂CH₂Br

A-223
CCl₂CH₂CH₃

A-224
CF₂CH₂CH₃

A-225
CH₂CH₂CHF₂

A-226
CH₂CH₂CHCl₂

A-227
CH₂CH₂CF₃

A-228
CH₂CH₂CCl₃

A-229
CF₂CF₂CF₃

A-230
CCl₂CCl₂CCl₃

A-231
CH(CH₃)CF₃

A-232
CH(CH₃)CH₂F

A-233
CH(CH₃)CH₂Cl

A-234
CH(CH₃)CH₂Br

A-235
CH(CH₃)CHF₂

A-236
CH(CH₃)CHCl₂

A-237
CH(CH₂F)₂

A-238
CH(CH₂Cl)₂

A-239
CH(CH₂Br)₂

A-240
CH(CHF₂)₂

A-241
CH(CHCl₂)₂

A-242
CHFCH₂CH₂CH₃

A-243
CHClCH₂CH₂CH₃

A-244
CH₂CHFCH₂CH₃

A-245
CH₂CHClCH₂CH₃

A-246
CH₂CH₂CHFCH₃

A-247
CH₂CH₂CHClCH₃

A-248
CH₂CH₂CH₂CH₂F

A-249
CH₂CH₂CH₂CH₂Cl

A-250
CH₂CH₂CH₂CH₂Br

A-251
CCl₂CH₂CH₂CH₃

A-252
CF₂CH₂CH₂CH₃

A-253
CH₂CH₂CH₂CHF₂

A-254
CH₂CH₂CH₂CHCl₂

A-255
CH₂CH₂CH₂CF₃

A-256
CH₂CH₂CH₂CCl₃

A-257
CF₂CF₂CF₂CF₃

A-258
CCl₂CCl₂CCl₂CCl₃

A-259
CH(CH₃)CH₂CH₂F

A-260
CH(CH₃)CH₂CH₂Cl

A-261
CH(CH₃)CH₂CH₂Br

A-262
CH(CH₃)CH₂CF₃

A-263
CHFCH₂CH₂CH₂CH₃

A-264
CHClCH₂CH₂CH₂CH₃

A-265
CH₂CHFCH₂CH₂CH₃

A-266
CH₂CHClCH₂CH₂CH₃

A-267
CH₂CH₂CHFCH₂CH₃

A-268
CH₂CH₂CHClCH₂CH₃

A-269
CH₂CH₂CH₂CHFCH₃

A-270
CH₂CH₂CH₂CHClCH₃

A-271
CH₂CH₂CH₂CH₂CH₂F

A-272
CH₂CH₂CH₂CH₂CH₂Cl

A-273
CH₂CH₂CH₂CH₂CH₂Br

A-274
CCl₂CH₂CH₂CH₂CH₃

A-275
CF₂CH₂CH₂CH₂CH₃

A-276
CH₂CH₂CH₂CH₂CHF₂

A-277
CH₂CH₂CH₂CH₂CHCl₂

A-278
CH₂CH₂CH₂CH₂CF₃

A-279
CH₂CH₂CH₂CH₂CCl₃

A-280
CF₂CF₂CF₂CF₂CF₃

A-281
CCl₂CCl₂CCl₂CCl₂CCl₃

A-282
CH(CH₃)CH₂CH₂CH₂F

A-283
CH(CH₃)CH₂CH₂CH₂Cl

A-284
CH(CH₃)CH₂CH₂CH₂Br

A-285
CH(CH₃)CH₂CH₂CF₃

A-286
CHFCH₂CH₂CH₂CH₂CH₃

A-287
CHClCH₂CH₂CH₂CH₂CH₃

A-288
CH₂CHFCH₂CH₂CH₂CH₃

A-289
CH₂CHClCH₂CH₂CH₂CH₃

A-290
CH₂CH₂CHFCH₂CH₂CH₃

A-291
CH₂CH₂CHClCH₂CH₂CH₃

A-292
CH₂CH₂CH₂CHFCH₂CH₃

A-293
CH₂CH₂CH₂CHClCH₂CH₃

A-294
CH₂CH₂CH₂CH₂CHFCH₃

A-295
CH₂CH₂CH₂CH₂CHClCH₃

A-296
CH₂CH₂CH₂CH₂CH₂CH₂F

A-297
CH₂CH₂CH₂CH₂CH₂CH₂Cl

A-298
CH₂CH₂CH₂CH₂CH₂CH₂Br

A-299
CCl₂CH₂CH₂CH₂CH₂CH₃

A-300
CF₂CH₂CH₂CH₂CH₂CH₃

A-301
CH₂CH₂CH₂CH₂CH₂CHF₂

A-302
CH₂CH₂CH₂CH₂CH₂CHCl₂

A-303
CH₂CH₂CH₂CH₂CH₂CF₃

A-304
CH₂CH₂CH₂CH₂CH₂CCl₃

A-305
CF₂CF₂CF₂CF₂CF₂CF₃

A-306
CCl₂CCl₂CCl₂CCl₂CCl₂CCl₃

A-307
CH(CH₃)CH₂CH₂CH₂CH₂F

A-308
CH(CH₃)CH₂CH₂CH₂CH₂Cl

A-309
CH(CH₃)CH₂CH₂CH₂CH₂Br

A-310
CH(CH₃)CH₂CH₂CH₂CF₃

A-311
CHFCH₂CH₂CH₂CH₂CH₂CH₃

A-312
CHClCH₂CH₂CH₂CH₂CH₂CH₃

A-313
CH₂CHFCH₂CH₂CH₂CH₂CH₃

A-314
CH₂CHClCH₂CH₂CH₂CH₂CH₃

A-315
CH₂CH₂CH₂CHFCH₂CH₂CH₃

A-316
CH₂CH₂CH₂CHClCH₂CH₂CH₃

A-317
CH₂CH₂CH₂CH₂CHFCH₂CH₃

A-318
CH₂CH₂CH₂CH₂CHClCH₂CH₃

A-319
CH₂CH₂CH₂CH₂CH₂CHFCH₃

A-320
CH₂CH₂CH₂CH₂CH₂CHClCH₃

A-321
CH₂CH₂CH₂CH₂CH₂CH₂CH₂F

A-322
CH₂CH₂CH₂CH₂CH₂CH₂CH₂Cl

A-323
CH₂CH₂CH₂CH₂CH₂CH₂CH₂Br

A-324
CCl₂CH₂CH₂CH₂CH₂CH₂CH₃

A-325
CF₂CH₂CH₂CH₂CH₂CH₂CH₃

A-326
CH₂CH₂CH₂CH₂CH₂CH₂CHF₂

A-327
CH₂CH₂CH₂CH₂CH₂CH₂CHCl₂

A-328
CH₂CH₂CH₂CH₂CH₂CH₂CF₃

A-329
CH₂CH₂CH₂CH₂CH₂CH₂CCl₃

A-330
CF₂CF₂CF₂CF₂CF₂CF₂CF₃

A-331
CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₃

A-332
CH(CH₃)CH₂CH₂CH₂CH₂CH₂F

A-333
CH(CH₃)CH₂CH₂CH₂CH₂CH₂Cl

A-334
CH(CH₃)CH₂CH₂CH₂CH₂CH₂Br

A-335
CH(CH₃)CH₂CH₂CH₂CH₂CF₃

A-336
CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-337
CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-338
CH₂CHFCH₂CH₂CH₂CH₂CH₂CH₃

A-339
CH₂CHClCH₂CH₂CH₂CH₂CH₂CH₃

A-340
CH₂CH₂CHFCH₂CH₂CH₂CH₂CH₃

A-341
CH₂CH₂CHClCH₂CH₂CH₂CH₂CH₃

A-342
CH₂CH₂CH₂CH₂CHFCH₂CH₂CH₃

A-343
CH₂CH₂CH₂CH₂CHClCH₂CH₂CH₃

A-344
CH₂CH₂CH₂CH₂CH₂CHFCH₂CH₃

A-345
CH₂CH₂CH₂CH₂CH₂CHClCH₂CH₃

A-346
CH₂CH₂CH₂CH₂CH₂CH₂CHFCH₃

A-347
CH₂CH₂CH₂CH₂CH₂CH₂CHClCH₃

A-348
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂F

A-349
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂Cl

A-350
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂Br

A-351
CCl₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-352
CF₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-353
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHF₂

A-354
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHCl₂

A-355
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CF₃

A-356
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CCl₃

A-357
CF₂CF₂CF₂CF₂CF₂CF₂CF₂CF₃

A-358
CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₃

A-359
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂F

A-360
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂Cl

A-361
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂Br

A-362
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CF₃

A-363
CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-364
CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-365
CH₂CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-366
CH₂CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-367
CH₂CH₂CHFCH₂CH₂CH₂CH₂CH₂CH₃

A-368
CH₂CH₂CHClCH₂CH₂CH₂CH₂CH₂CH₃

A-369
CH₂CH₂CH₂CHFCH₂CH₂CH₂CH₂CH₃

A-370
CH₂CH₂CH₂CHClCH₂CH₂CH₂CH₂CH₃

A-371
CH₂CH₂CH₂CH₂CH₂CHFCH₂CH₂CH₃

A-372
CH₂CH₂CH₂CH₂CH₂CHClCH₂CH₂CH₃

A-373
CH₂CH₂CH₂CH₂CH₂CH₂CHFCH₂CH₃

A-374
CH₂CH₂CH₂CH₂CH₂CH₂CHClCH₂CH₃

A-375
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHFCH₃

A-376
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHClCH₃

A-377
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂F

A-378
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂Cl

A-379
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂Br

A-380
CCl₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-381
CF₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-382
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHF₂

A-383
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHCl₂

A-384
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CF₃

A-385
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CCl₃

A-386
CF₂CF₂CF₂CF₂CF₂CF₂CF₂CF₂CF₃

A-387
CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₃

A-388
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂F

A-389
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂Cl

A-390
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂Br

A-391
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CF₃

A-392
CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-393
CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-394
CH₂CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-395
CH₂CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-396
CH₂CH₂CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-397
CH₂CH₂CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-398
CH₂CH₂CH₂CHFCH₂CH₂CH₂CH₂CH₂CH₃

A-399
CH₂CH₂CH₂CHClCH₂CH₂CH₂CH₂CH₂CH₃

A-400
CH₂CH₂CH₂CH₂CHFCH₂CH₂CH₂CH₂CH₃

A-401
CH₂CH₂CH₂CH₂CHClCH₂CH₂CH₂CH₂CH₃

A-402
CH₂CH₂CH₂CH₂CH₂CH₂CHFCH₂CH₂CH₃

A-403
CH₂CH₂CH₂CH₂CH₂CH₂CHClCH₂CH₂CH₃

A-404
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHFCH₂CH₃

A-405
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHClCH₂CH₃

A-406
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHFCH₃

A-407
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHClCH₃

A-408
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂F

A-409
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂Br

A-410
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂Cl

A-411
CCl₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-412
CF₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-413
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHF₂

A-414
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CHCl₂

A-415
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CF₃

A-416
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CCl₃

A-417
CF₂CF₂CF₂CF₂CF₂CF₂CF₂CF₂CF₂CF₃

A-418
CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₂CCl₃

A-419
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂F

A-420
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂Cl

A-421
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂Br

A-422
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CF₃

A-423
CH═CH₂

A-424
CH₂CH═CH₂

A-425
CH═CHCH₃

A-426
C(CH₃)═CH₂

A-427
CH₂CH₂CH═CH₂

A-428
CH₂CH═CHCH₃

A-429
CH═CHCH₂CH₃

A-430
CH(CH₃)CH═CH₂

A-431
C(CH₃)═CHCH₃

A-432
CH═C(CH₃)₂

A-433
CH₂CH₂CH₂CH═CH₂

A-434
CH₂CH₂CH═CHCH₃

A-435
CH₂CH═CHCH₂CH₃

A-436
CH═CHCH₂CH₂CH₃

A-437
CH(CH₃)CH₂CH═CH₂

A-438
CH₂C(CH₃)═CHCH₃

A-439
CH₂CH═C(CH₃)₂

A-440
CH₂CH₂CH₂CH₂CH═CH₂

A-441
CH₂CH₂CH₂CH═CHCH₃

A-442
CH₂CH₂CH═CHCH₂CH₃

A-443
CH₂CH═CHCH₂CH₂CH₃

A-444
CH═CHCH₂CH₂CH₂CH₃

A-445
CH(CH₃)CH₂CH₂CH═CH₂

A-446
CH(CH₃)CH₂CH═CHCH₃

A-447
CH₂C(CH₃)═CHCH₂CH₃

A-448
CH₂CH₂CH═C(CH₃)₂

A-449
CH₂CH₂CH₂CH₂CH₂CH═CH₂

A-450
CH₂CH₂CH₂CH₂CH═CHCH₃

A-451
CH₂CH₂CH₂CH═CHCH₂CH₃

A-452
CH₂CH₂CH═CHCH₂CH₂CH₃

A-453
CH₂CH═CHCH₂CH₂CH₂CH₃

A-454
CH═CHCH₂CH₂CH₂CH₂CH₃

A-455
CH(CH₃)CH₂CH₂CH₂CH═CH₂

A-456
CH(CH₃)CH₂CH₂CH═CHCH₃

A-457
C(CH₃)═CHCH₂CH₂CH₂CH₃

A-458
CH₂CH₂CH₂CH═C(CH₃)₂

A-459
CH₂CH₂CH₂CH₂CH₂CH₂CH═CH₂

A-460
CH₂CH₂CH₂CH₂CH₂CH═CHCH₃

A-461
CH₂CH₂CH₂CH₂CH═CHCH₂CH₃

A-462
CH₂CH₂CH₂CH═CHCH₂CH₂CH₃

A-463
CH₂CH₂CH═CHCH₂CH₂CH₂CH₃

A-464
CH₂CH═CHCH₂CH₂CH₂CH₂CH₃

A-465
CH═CHCH₂CH₂CH₂CH₂CH₂CH₃

A-466
CH(CH₃)CH₂CH₂CH₂CH₂CH═CH₂

A-467
CH(CH₃)CH₂CH₂CH₂CH═CHCH₃

A-468
C(CH₃)═CHCH₂CH₂CH₂CH₂CH₃

A-469
CH₂CH₂CH₂CH₂CH═C(CH₃)₂

A-470
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH═CH₂

A-471
CH₂CH₂CH₂CH₂CH₂CH₂CH═CHCH₃

A-472
CH₂CH₂CH₂CH₂CH₂CH═CHCH₂CH₃

A-473
CH₂CH₂CH₂CH₂CH═CHCH₂CH₂CH₃

A-474
CH₂CH₂CH₂CH═CHCH₂CH₂CH₂CH₃

A-475
CH₂CH₂CH═CHCH₂CH₂CH₂CH₂CH₃

A-476
CH₂CH═CHCH₂CH₂CH₂CH₂CH₂CH₃

A-477
CH═CHCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-478
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH═CH₂

A-479
CH(CH₃)CH₂CH₂CH₂CH₂CH═CHCH₃

A-480
C(CH₃)═CHCH₂CH₂CH₂CH₂CH₂CH₃

A-481
CH₂CH₂CH₂CH₂CH₂CH═C(CH₃)₂

A-482
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH═CH₂

A-483
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH═CHCH₃

A-484
CH₂CH₂CH₂CH₂CH₂CH₂CH═CHCH₂CH₃

A-485
CH₂CH₂CH₂CH₂CH₂CH═CHCH₂CH₂CH₃

A-486
CH₂CH₂CH₂CH₂CH═CHCH₂CH₂CH₂CH₃

A-487
CH₂CH₂CH₂CH═CHCH₂CH₂CH₂CH₂CH₃

A-488
CH₂CH₂CH═CHCH₂CH₂CH₂CH₂CH₂CH₃

A-489
CH₂CH═CHCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-490
CH═CHCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-491
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH═CH₂

A-492
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH═CHCH₃

A-493
C(CH₃)═CHCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-494
CH₂CH₂CH₂CH₂CH₂CH₂CH═C(CH₃)₂

A-495
C≡CH

A-496
CH₂C≡CH

A-497
C≡CCH₃

A-498
CH₂CH₂C≡CH

A-499
CH₂C≡CCH₃

A-500
C≡CCH₂CH₃

A-501
CH(CH₃)C≡CH

A-502
CH₂CH₂CH₂C≡CH

A-503
CH₂CH₂C≡CCH₃

A-504
CH₂C≡CCH₂CH₃

A-505
C≡CCH₂CH₂CH₃

A-506
CH(CH₃)CH₂C≡CH

A-507
CH₂CH₂CH₂CH₂C≡CH

A-508
CH₂CH₂CH₂C≡CCH₃

A-509
CH₂CH₂C≡CCH₂CH₃

A-510
CH₂C≡CCH₂CH₂CH₃

A-511
C≡CCH₂CH₂CH₂CH₃

A-512
CH(CH₃)CH₂CH₂C≡CH

A-513
CH(CH₃)CH₂C≡CCH₃

A-514
CH₂CH₂CH₂CH₂CH₂C≡CH

A-515
CH₂CH₂CH₂CH₂C≡CCH₃

A-516
CH₂CH₂CH₂C≡CCH₂CH₃

A-517
CH₂CH₂C≡CCH₂CH₂CH₃

A-518
CH₂C≡CCH₂CH₂CH₂CH₃

A-519
C≡CCH₂CH₂CH₂CH₂CH₃

A-520
CH(CH₃)CH₂CH₂CH₂C≡CH

A-521
CH(CH₃)CH₂CH₂C≡CCH₃

A-522
CH(CH₃)CH₂C≡CCH₂CH₃

A-523
CH₂CH₂CH₂CH₂CH₂CH₂C≡CH

A-524
CH₂CH₂CH₂CH₂CH₂C≡CCH₃

A-525
CH₂CH₂CH₂CH₂C≡CCH₂CH₃

A-526
CH₂CH₂CH₂C≡CCH₂CH₂CH₃

A-527
CH₂CH₂C≡CCH₂CH₂CH₂CH₃

A-528
CH₂C≡CCH₂CH₂CH₂CH₂CH₃

A-529
C≡CCH₂CH₂CH₂CH₂CH₂CH₃

A-530
CH(CH₃)CH₂CH₂CH₂CH₂C≡CH

A-531
CH(CH₃)CH₂CH₂CH₂C≡CCH₃

A-532
CH₂CH₂CH₂CH₂CH₂CH₂CH₂C≡CH

A-533
CH₂CH₂CH₂CH₂CH₂CH₂C≡CCH₃

A-534
CH₂CH₂CH₂CH₂CH₂C≡CCH₂CH₃

A-535
CH₂CH₂CH₂CH₂C≡CCH₂CH₂CH₃

A-536
CH₂CH₂CH₂C≡CCH₂CH₂CH₂CH₃

A-537
CH₂CH₂C≡CCH₂CH₂CH₂CH₂CH₃

A-538
CH₂C≡CCH₂CH₂CH₂CH₂CH₂CH₃

A-539
C≡CCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-540
CH(CH₃)CH₂CH₂CH₂CH₂CH₂C≡CH

A-541
CH(CH₃)CH₂CH₂CH₂CH₂C≡CCH₃

A-542
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂C≡CH

A-543
CH₂CH₂CH₂CH₂CH₂CH₂CH₂C≡CCH₃

A-544
CH₂CH₂CH₂CH₂CH₂CH₂C≡CCH₂CH₃

A-545
CH₂CH₂CH₂CH₂CH₂C≡CCH₂CH₂CH₃

A-546
CH₂CH₂CH₂CH₂C≡CCH₂CH₂CH₂CH₃

A-547
CH₂CH₂CH₂C≡CCH₂CH₂CH₂CH₂CH₃

A-548
CH₂CH₂C≡CCH₂CH₂CH₂CH₂CH₂CH₃

A-549
CH₂C≡CCH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-550
C≡CCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₃

A-551
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂C≡CH

A-552
CH(CH₃)CH₂CH₂CH₂CH₂CH₂C≡CCH₃

A-553
CH₂CH₂CH₂CH₂CH₂CN

A-554
CH(CH₃)CH₂CH₂CH₂CN

A-555
CH₂CH(CH₃)CH₂CH₂CN

A-556
CH₂CH₂CH(CH₃)CH₂CN

A-557
CH₂CH₂CH(CH₃)CH₂CN

A-558
CH(CH₃)CH(CH₃)CH₂CN

A-559
CH(CH₃)CH(CH₃)CH₂CN

A-560
CH₂C(CH₃)₂CH₂CN

A-561
CH₂CH₂CH₂CH₂CH₂CH₂CN

A-562
CH(CH₃)CH₂CH₂CH₂CH₂CN

A-563
CH₂CH(CH₃)CH₂CH₂CH₂CN

A-564
CH₂CH₂CH(CH₃)CH₂CH₂CN

A-565
CH₂CH₂CH(CH₃)₂CH₂CH₂CN

A-566
CH₂CH₂CH₂CH(CH₃)CH₂CN

A-567
CH(CH₃)CH(CH₃)CH₂CH₂CN

A-568
CH(CH₃)CH₂CH(CH₃)CH₂CN

A-569
CH₂CH₂C(CH₃)₂CH₂CN

A-570
CH(CH₃)CH₂CH(CH₃)CH₂CN

A-571
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-572
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-573
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-574
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-575
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-576
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-577
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-578
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CN

A-579
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CN

A-580
CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-581
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CN

A-582
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CN

A-583
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CN

A-584
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-585
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-586
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-587
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-588
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-589
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-590
CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-591
CH₂CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-592
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CN

A-593
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CN

A-594
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CN

A-595
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CN

A-596
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CN

A-597
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CN

A-598
CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CN

A-599
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-600
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-601
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-602
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-603
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-604
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-605
CH₂CH₂CH₂CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-606
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-607
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CN

A-608
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CH₂CN

A-609
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-610
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CN

A-611
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-612
CH(CH₃)CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-613
CH₂CH(CH₃)CH₂CH₂CH(CH₃)₂CH₂CN

A-614
CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-615
CH₂CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CN

A-616
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-617
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-618
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-619
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-620
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-621
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-622
CH₂CH₂CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-623
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-624
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-625
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CH₂CH₂CN

A-626
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-627
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-628
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-629
CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-630
CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-631
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-632
CH(CH₃)CH₂CH₂CH₂CH₂CH₂C(CH₃)CH₂CN

A-633
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-634
CH(CH₃)CH₂CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-635
CH₂CH(CH₃)CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-636
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-637
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-638
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-639
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-640
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-641
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-642
CH₂CH₂CH₂CH₂CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-643
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-644
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-645
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CH₂CH₂CH₂CN

A-646
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-647
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-648
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-649
CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-650
CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-651
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-652
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-653
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-654
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-655
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-656
CH₂CH(CH₃)CH₂CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-657
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-658
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-659
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-660
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-661
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-662
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-663
CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-664
CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-665
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-666
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-667
CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CN

A-668
CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-669
CH₂CH(CH₃)CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-670
CH₂CH₂CH₂C(CH₃)₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-671
CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-672
CH(CH₃)CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-673
CH(CH₃)CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CN

A-674
CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂CN

A-675
CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CN

A-676
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-677
CH(CH₃)CH₂CH₂CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-678
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CN

A-679
CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-680
CH₂CH₂CH₂CH(CH₃)CH₂CH₂CH₂CH(CH₃)CH₂CH₂CN

A-681
CH₂CH(CH₃)CH₂CH₂CH₂CH₂CH₂C(CH₃)₂CH₂CN

A-682
CHFCH₂CN

A-683
CHClCH₂CN

A-684
CCl₂CH₂CN

A-685
CF₂CH₂CN

A-686
CHFCH₂CH₂CN

A-687
CHClCH₂CH₂CN

A-688
CCl₂CH₂CH₂CN

A-689
CF₂CH₂CH₂CN

A-690
CHFCH₂CH₂CH₂CN

A-691
CHClCH₂CH₂CH₂CN

A-692
CCl₂CH₂CH₂CH₂CN

A-693
CF₂CH₂CH₂CH₂CN

A-694
CHFCH₂CH₂CH₂CH₂CN

A-695
CHClCH₂CH₂CH₂CH₂CN

A-696
CCl₂CH₂CH₂CH₂CH₂CN

A-697
CF₂CH₂CH₂CH₂CH₂CN

A-698
CHFCH₂CH₂CH₂CH₂CH₂CN

A-699
CHClCH₂CH₂CH₂CH₂CH₂CN

A-700
CCl₂CH₂CH₂CH₂CH₂CH₂CN

A-701
CF₂CH₂CH₂CH₂CH₂CH₂CN

A-702
CHFCH₂CH₂CH₂CH₂CH₂CH₂CN

A-703
CHClCH₂CH₂CH₂CH₂CH₂CH₂CN

A-704
CCl₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-705
CF₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-706
CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-707
CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-708
CCl₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-709
CF₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-710
CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-711
CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-712
CCl₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-713
CF₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-714
CHFCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-715
CHClCH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-716
CCl₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

A-717
CF₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CH₂CN

The compounds I are suitable as fungicides. They are distinguished by an outstanding effectiveness against a broad spectrum of phytopathogenic fungi from the classes of the Ascomycetes, Deuteromycetes, Oomycetes and Basidiomycetes, especially from the class of the Oomycetes. Some are systemically effective and they can be used in plant protection as foliar fungicides, fungicides for seed dressing and soil fungicides.

They are particularly important in the control of a multitude of fungi on various cultivated plants, such as wheat, rye, barley, oats, rice, corn, grass, bananas, cotton, soyabeans, coffee, sugar cane, vines, fruits, ornamental plants, and vegetables, such as cucumbers, beans, tomatoes, potatoes and cucurbits, and on the seeds of these plants.

They are especially suitable for controlling the following plant diseases:

- Alternaria species on vegetables, rapeseed, sugar beet and fruit and rice (for example A. solani or A. alternata on potato and other plants),
- Aphanomyces species on sugar beet and vegetables,
- Bipolaris and Drechslera species on corn, cereals, rice and lawns (for example D. teres on barley, D. tritci-repentis on wheat),
- Blumeria graminis (powdery mildew) on cereals,
- Botrytis cinerea (gray mold) on strawberries, vegetables, flowers and grapevines,
- Bremia lactucae on lettuce,
- Cercospora species on corn, soybeans, rice and sugar beet (for example C. beticula on sugar beet),
- Cochliobolus species on corn, cereals, rice (for example Cochliobolus sativus on cereals, Cochliobolus miyabeanus on rice),
- Colletotricum species on soybeans, cotton and other plants (for example C. acutatum on various plants),
- Exserohilum speciea on corn,
- Erysiphe cichoracearum and Sphaerotheca fuliginea on cucurbits,
- Fusarium and Verticillium species (for example V. dahliae) on various plants (for example F. graminearum on wheat),
- Gaeumanomyces graminis on cereals,
- Gibberella species on cereals and rice (for example Gibberella fujikuroi on rice),
- Grainstaining complex on rice,
- Helminthosporium species (for example H. graminicola) on corn and rice,
- Michrodochium nivale on cereals,
- Mycosphaerella species on cereals, bananas and peanuts (M. graminicola on wheat, M. fijiesis on bananas),
- Phakopsara pachyrhizi and Phakopsara meibomiae on soybeans,
- Phomopsis species on soybeans, sunflowers and grapevines (P. viticola on grapevines, P. helianthii on sunflowers),
- Phytophthora infestans on potatoes and tomatoes,
- Plasmopara viticola on grapevines,
- Podosphaera leucotricha on apples,
- Pseudocercosporella herpotrichoides on cereals,
- Pseudoperonospora species on hops and cucurbits (for example P. cubenis on cucumbers),
- Puccinia species on cereals, corn and asparagus (P. triticina and P. striformis on wheat, P. asparagi on asparagus),
- Pyrenophora species on cereals,
- Pyricularia oryzae, Corticium sasakii, Sarocladium oryzae, S. attenuatum, Entyloma oryzae on rice,
- Pyricularia grisea on lawns and cereals,
- Pythium spp. on lawns, rice, corn, cotton, rapeseed, sunflowers, sugar beet, vegetables and other plants,
- Rhizoctonia-species (for example R. solani) on cotton, rice, potatoes, lawns, corn, rapeseed, potatoes, sugar beet, vegetables and other plants,
- Sclerotinia species (for example S. sclerotiorum) on rapeseed, sunflowers and other plants,
- Septoria tritici and Stagonospora nodorum on wheat,
- Erysiphe (syn. Uncinula necator) on grapevines,
- Setospaeria species on corn and lawns,
- Sphacelotheca reilinia on corn,
- Thievaliopsis species on soybeans and cotton,
- Tilletia species on cereals,
- Ustilago species on cereals, corn and sugar beet and
- Venturia species (scab) on apples and pears (for example V. inaequalis on apples).

They are particularly suitable for controlling harmful fungi from the class of the Oomycetes, such as Peronospora species, Phytophthora species, Plasmopara viticola and Pseudoperonospora species.

The compounds I are furthermore suitable for controlling harmful fungi in the protection of materials (for example wood, paper, paint dispersions, fibers or fabrics) and in the protection of stored products. In the protection of wood, particular attention is paid to the following harmful fungi: Ascomycetes, such as Ophiostoma spp., Ceratocystis spp., Aureobasidium pullulans, Sclerophoma spp., Chaetomium spp., Humicola spp., Petriella spp., Trichurus spp.; Basidiomycetes, such as Coniophora spp., Coriolus spp., Gloeophyllum spp., Lentinus spp., Pleurotus spp., Poria spp., Serpula spp. and Tyromyces spp., Deuteromycetes, such as Aspergillus spp., Cladosporium spp., Penicillium spp., Trichoderma spp., Alternaria spp., Paecilomyces spp. and Zygomycetes, such as Mucor spp., additionally in the protection of materials the following yeasts: Candida spp. and Saccharomyces cerevisae.

The compounds I are employed by treating the fungi or the plants, seeds, materials or soil to be protected from fungal attack with a fungicidally effective amount of the active compounds. The application can be carried out both before and after the infection of the materials, plants or seeds by the fungi.

The fungicidal compositions generally comprise between 0.1 and 95%, preferably between 0.5 and 90%, by weight of active compound.

When employed in plant protection, the amounts applied are, depending on the kind of effect desired, between 0.01 and 2.0 kg of active compound per ha.

In seed treatment, amounts of active compound of 1 to 1000 g/100 kg, preferably 5 to 100 g/100 kg of seed are generally required.

When used in the protection of materials or stored products, the amount of active compound applied depends on the kind of application area and on the desired effect. Amounts customarily applied in the protection of materials are, for example, 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active compound per cubic meter of treated material.

The compounds of the formula I can be present in various crystal modifications which may differ in their biological activity. They also form part of the subject matter of the present invention.

The compounds I can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules. The application form depends on the particular purpose; in each case, it should ensure a fine and uniform distribution of the compound according to the invention.

The formulations are prepared in a known manner, for example by extending the active compound with solvents and/or carriers, if desired using emulsifiers and dispersants. Solvents/auxiliaries which are suitable are essentially:

- water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters. In principle, solvent mixtures may also be used,
- carriers such as ground natural minerals (for example kaolins, clays, talc, chalk) and ground synthetic minerals (for example highly disperse silica, silicates); emulsifiers such as nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignosulfite waste liquors and methylcellulose.

Suitable surfactants are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ethers, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ethers, tristearylphenyl polyglycol ethers, alkylaryl polyether alcohols, alcohol and fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose.

Suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, strongly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone and water.

Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.

Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers. Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.

In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compound. The active compounds are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).

The following are examples of formulations: 1. Products for dilution with water

A Water-Soluble Concentrates (SL, LS)

10 parts by weight of the active compounds are dissolved in 90 parts by weight of water or in a water-soluble solvent. As an alternative, wetting agents or other auxiliaries are added. The active compound dissolves upon dilution with water. In this way, a formulation having a content of 10% by weight of active compound is obtained.

B Dispersible Concentrates (DC)

20 parts by weight of the active compounds are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion. The active compound content is 20% by weight

C Emulsifiable Concentrates (EC)

15 parts by weight of the active compounds are dissolved in 75 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion. The formulation has an active compound content of 15% by weight.

D Emulsions (EW, EO, ES)

25 parts by weight of the active compounds are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of water by means of an emulsifying machine (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion. The formulation has an active compound content of 25% by weight.

E Suspensions (SC, OD, FS)

In an agitated ball mill, 20 parts by weight of the active compounds are comminuted with addition of 10 parts by weight of dispersants and wetting agents and 70 parts by weight of water or an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound. The active compound content in the formulation is 20% by weight.

F Water-Dispersible Granules and Water-Soluble Granules (WG, SG)

50 parts by weight of the active compounds are ground finely with addition of 50 parts by weight of dispersants and wetting agents and prepared as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound. The formulation has an active compound content of 50% by weight.

G Water-Dispersible Powders and Water-Soluble Powders (WP, SP, SS, WS)

75 parts by weight of the active compounds are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetting agents and silica gel. Dilution with water gives a stable dispersion or solution of the active compound. The active compound content of the formulation is 75% by weight.

H Gel Formulations

In a ball mill, 20 parts by weight of the active compounds, 10 parts by weight of dispersant, 1 part by weight of gelling agent and 70 parts by weight of water or an organic solvent are ground to give a fine suspension. On dilution with water, a stable suspension having an active compound content of 20% by weight is obtained.

2. Products to be Applied Undiluted
I Dustable Powders (DP, DS)

5 parts by weight of the active compounds are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product having an active compound content of 5% by weight.

J Granules (GR, FG, GG, MG)

0.5 part by weight of the active compounds is ground finely and associated with 99.5 parts by weight of carriers. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted having an active compound content of 0.5% by weight.

K ULV Solutions (UL)

10 parts by weight of the active compounds are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product to be applied undiluted having an active compound content of 10% by weight.

For seed treatment, use is usually made of water-soluble concentrates (LS), suspensions (FS), dustable powders (DS), water-dispersible and water-soluble powders (WS, SS), emulsions (ES), emulsifiable concentrates (EC) and gel formulations (GF). These formulations can be applied to the seed in undiluted form or, preferably, diluted. Application can be carried out prior to sowing.

The active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; the intention is to ensure in each case the finest possible distribution of the active compounds according to the invention.

Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. Alternatively, it is possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.

The active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1%.

The active compounds may also be used successfully in the ultra-low-volume process (ULV), by which it is possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.

Various types of oils, wetters, adjuvants, herbicides, fungicides, other pesticides, or bactericides may be added to the active compounds, if appropriate not until immediately prior to use (tank mix). These agents can be admixed with the agents according to the invention in a weight ratio of 1:100 to 100:1, preferably 1:10 to 10:1.

Suitable adjuvants in this sense are in particular: organically modified polysiloxanes, for example Break Thru S 240®; alcohol alkoxylates, for example Atplus 245®, Atplus MBA 1303®, Plurafac LF 300® and Lutensol ON 30®; EO/PO block polymers, for example Pluronic RPE 2035® and Genapol B®; alcohol ethoxylates, for example Lutensol XP 80®; and sodium dioctylsulfosuccinate, for example Leophen RA®.

The compositions according to the invention can, in the use form as fungicides, also be present together with other active compounds, e.g. with herbicides, insecticides, growth regulators, fungicides or else with fertilizers. Mixing the compounds I or the compositions comprising them in the application form as fungicides with other active compounds, in particular fungicides, it is in many cases possible to broaden the activity spectrum or to prevent the development of resistance. In many cases, synergistic effects are obtained.

The following list of fungicides, in conjunction with which the compounds according to the invention can be used, is intended to illustrate the possible combinations but does not limit them:

Strobilurins

azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, metominostrobin, picoxystrobin, pyraclostrobin, trifloxystrobin, orysastrobin, methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)ethyl]benzyl)carbamate, methyl (2-chloro-5-[1-(6-methylpyridin-2-ylmethoxyimino)ethyl]benzyl)carbamate, methyl 2-(ortho-(2,5-dimethylphenyloxymethylene)phenyl)-3-methoxyacrylate;

Carboxamides

- carboxanilides: benalaxyl, benodanil, boscalid, carboxin, mepronil, fenfuram, fenhexamid, flutolanil, furametpyr, metalaxyl, ofurace, oxadixyl, oxycarboxin, penthiopyrad, thifluzamide, tiadinil, N-(4′-bromobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4′-trifluoromethylbiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(4′-chloro-3′-fluorobiphenyl-2-yl)-4-difluoromethyl-2-methylthiazole-5-carboxamide, N-(3′,4′-dichloro-4-fluorobiphenyl-2-yl)-3-difluoromethyl-1-methylpyrazole-4-carboxamide, N-(2-cyanophenyl)-3,4-dichloroisothiazole-5-carboxamide;
- carboxylic acid morpholides: dimethomorph, flumorph;
- benzamides: flumetover, fluopicolide (picobenzamid), zoxamide;
- other carboxamides: carpropamid, diclocymet, mandipropamid, N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl)ethyl)-2-methanesulfonylamino-3-methylbutyramide, N-(2-(4-[3-(4-chlorophenyl)prop-2-ynyloxy]-3-methoxyphenyl)ethyl)-2-ethanesulfonylamino-3-methylbutyramide; azoles
- triazoles: bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, enilconazole, epoxiconazole, fenbuconazole, flusilazole, fluquinconazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myciobutanil, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimenol, triadimefon, triticonazole;
- imidazoles: cyazofamid, imazalil, pefurazoate, prochloraz, triflumizole;
- benzimidazoles: benomyl, carbendazim, fuberidazole, thiabendazole;
- others: ethaboxam, etridiazole, hymexazole;

Nitrogenous Heterocyclyl Compounds

- pyridines: fluazinam, pyrifenox, 3-[5-(4-chlorophenyl)-2,3-dimethylisoxazolidin-3-yl]-pyridine;
- pyrimidines: bupirimate, cyprodinil, ferimzone, fenarimol, mepanipyrim, nuarimol,
- pyrimethanil;
- piperazines: triforine;
- pyrroles: fludioxonil, fenpiclonil;
- morpholines: aldimorph, dodemorph, fenpropimorph, tridemorph;
- dicarboximides: iprodione, procymidone, vinclozolin;
  - others: acibenzolar-S-methyl, anilazine, captan, captafol, dazomet, diclomezine, fenoxanil, folpet, fenpropidin, famoxadone, fenamidone, octhilinone, probenazole, proquinazid, pyroquilon, quinoxyfen, tricyclazole, 5-chloro-7-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine, 2-butoxy-6-iodo-3-propylchromen-4-one, N,N-dimethyl-3-(3-bromo-6-fluoro-2-methylindole-1-sulfonyl)-[1,2,4]triazole-1-sulfonamide;

Carbamates and Dithiocarbamates

- dithiocarbamates: ferbam, mancozeb, maneb, metiram, metam, propineb, thiram, zineb, ziram;
  - carbamates: diethofencarb, flubenthiavalicarb, iprovalicarb, propamocarb, methyl 3-(4-chlorophenyl)-3-(2-isopropoxycarbonylamino-3-methylbutyrylamino)propionate, 4-fluorophenyl N-(1-(1-(4-cyanophenyl)ethanesulfonyl)but-2-yl)carbamate;

Other Fungicides

- guanidines: dodine, iminoctadine, guazatine;
- antibiotics: kasugamycin, polyoxins, streptomycin, validamycin A;
- organometallic compounds: fentin salts;
- sulfur-containing heterocyclyl compounds: isoprothiolane, dithianon;
- organophosphorus compounds: edifenphos, fosetyl, fosetyl-aluminum, iprobenfos, pyrazophos, tolclofos-methyl, phosphorous acid and its salts;
- organochlorine compounds: thiophanate-methyl, chlorothalonil, dichlofluanid, tolylfluanid, flusulfamide, phthalide, hexachlorobenzene, pencycuron, quintozene;
- nitrophenyl derivatives: binapacryl, dinocap, dinobuton;
- inorganic active compounds: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur;
- others: spiroxamine, cyflufenamid, cymoxanil, metrafenone.

SYNTHESIS EXAMPLES

The procedures described in the following synthesis examples were used to prepare further compounds I by appropriate modification of the starting compounds. The compounds thus obtained are listed in the following tables, together with physical data.

Example 1
Preparation of ethyl 2-propionyldecanoate

32 g of ethylpropionyl acetate were added to 250 ml of an ethanolic NaOH solution (4.4% strength), and the mixture was stirred at 20-25° C. for 15 min. 63.6 g of 1-iodoctane were then added dropwise, and the entire solution was heated under reflux for 12 hours. The solvent was removed by distillation, the residue was then taken up in ethyl acetate, washed with Water and subsequently dried, and the volatile components were removed. Chromatography on silica gel (cyclohexane:ethyl acetate) of the residue gave 27 g of the title compound as a yellow oil.

Example 2
Preparation of 6-ethyl-2-mercapto-5-octylpyrimidin-4-ol

19.9 g of the ester from Ex. 1 were added to 38.9 ml of sodium methoxide solution (30% strength) in 70 ml of methanol, 8.2 g of thiourea were then added and the mixture was heated under reflux for 12 hours. The solvent was removed by distillation, and the residue was then dissolved in water and the solution was adjusted to pH 5 using glacial acetic acid. The resulting precipitate was filtered off, washed with water and dried. This gave 17.4 g of the title compound as yellow crystals.

Example 3
Preparation of 6-ethyl-2-methylsulfanyl-5-octylpyrimidin-4-ol

6 g of 2-mercaptopyrimidinol from Ex. 2 were dissolved in 3% strength aqueous NaOH, and 3.46 g of iodomethane were added dropwise at 5-10° C. The reaction solution was stirred at 20 to 25° C. for about 18 hours. The reaction mixture was adjusted to pH 5 using glacial acetic acid and extracted with ethyl acetate. After drying, the solvent was removed from the combined organic phases. This gave 5.6 g of the title compound as a yellow oil.

Example 4
Preparation of 4-chloro-6-ethyl-2-methylsulfanyl-5-octylpyrimidine

8.5 g of the pyrimidinol from Ex. 3 were initially charged in 60 ml of POCl₃and heated under reflux for 30 min. The solvent was distilled off, and the residue was then taken up in water and extracted with ethyl acetate. The combined organic phases were washed with water and then with 10% strength NaHCO₃solution and subsequently dried, and the solvent was removed. Chromatography on silica gel (cyclohexane/ethyl acetate) gave 7.7 g of the title compound as a light-brown oil.

Example 5
Preparation of 6-ethyl-2-methylsulfanyl-5-octylpyrimidin-4-ylamine

7.65 g of the pyrimidine from Ex. 4 and 0.68 g of phenol-4-sulfonic acid were together initially charged in ethanol in an autoclave. 30 ml of liquid ammonia were introduced at 20-25° C., and the autoclave was then stirred under 18.5 bar of autogenous pressure at 130° C. for 57 hours. The reaction mixture was filtered off and the solvent was removed from the filtrate. The residue that remained was taken up in ethyl acetate/water, and the organic phase was separated off and dried and the volatile constituents were removed. The residue gave, after chromatography on silica gel (cyclohexane/ethyl acetate), 4.9 g of the title compound as a colorless, wax-like product.

Example 6
Preparation of 6-ethyl-2-methylsulfonyl-5-octylpyrimidin-4-ylamine

1.0 g of the aminopyrimidine from Ex. 5 was dissolved in 15 ml of glacial acetic acid, and 0.06 g of sodium tungstate dihydrate was added at 20-25° C. At 20-30° C., 0.97 ml of 30% strength hydrogen peroxide solution was then added dropwise, and the solution was then stirred at 20-25° C. for 12 hours. Water was added, the mixture was filtered and the residue was then washed with water. The solid was taken up in dichloromethane and dehydrated azeotropically. Removal of the solvent gave 0.45 g of the title compound as colorless crystals of m.p. 90-92° C.

Example 7
Preparation of 6-ethyl-5-octyl-2-[1,2,4]-triazol-1-ylpyrimidin-4-ylamine [I-1]

32 mg of sodium hydride were initially charged in 5 ml of dimethyl sulfoxide (DMSO), and a solution of 77 mg of 1,2,4-triazole in 5 ml DMSO was added. After 1 hour of stirring at 20-25° C., a solution of 335 mg of the sulfone from Ex. 6 in 5 ml of DMSO was added dropwise, and the entire solution was stirred at 20-25° C. for 12 hours. Water was then added and the resulting precipitate was filtered off. The precipitate gave, after chromatography on silica gel, 152 mg of the title compound as a colorless crystalline material of m.p. 90-91° C.

Example 8
Preparation of 6-ethyl-5-octyl-2-pyrazol-1-yl-pyrimidin-4-ylamine [I-5]

18 mg of sodium hydride were initially charged in 2.5 ml of anhydrous tetrahydrofuran (THF), and a solution of 45 mg of pyrazole in 2.5 ml of anhydrous THF was added.

After 2 hours of stirring at 20-25° C., a solution of 200 mg of the sulfone from Ex. 6 in 2.5 ml of anhydrous THF was added dropwise, and the entire solution was stirred at 20-25° C. for 12 hours. Water was then added, and the solution was extracted with methyl tert-butyl ether (MTBE). The combined organic phases were dried and the solvent was removed. Preparative RP chromatography (CH₃CN/water mixture) gave 66 mg of the title compound as a colorless crystalline material of m.p. 62-63° C.

TABLE I

Compounds of the formula I

Phys. Data

(m.p. [° C.];

¹H-NMR [δ ppm];

No.
R¹
R²
R³
MS M⁺ [m/e])

I-1
(CH₂)₇CH₃
CH₂CH₃
1,2,4-triazol-1-yl
94

I-2
(CH₂)₇CH₃
CH₂CH₃
SO₂CH₃
90-92

I-3
(CH₂)₇CH₃
CH₂CH₃
SCH₃
4.75(s); 2.6(q);

2.5(s); 2.4(t);

1.45(m); 1.4-1.35

(m); 1.3(t); 0.9(t)

I-4
(CH₂)₇CH₃
CH₂CH₃
C(O)NH₂
7.9(s); 5.9(s);

5.4(s); 2.75(q);

2.5(t); 1.5(m);

1.45-1.2(m); 0.9(t)

I-5
(CH₂)₇CH₃
CH₂CH₃
pyrazol-1-yl
62-63

I-6
(CH₂)₇CH₃
CH₃
SCH₃
267.441

I-7
(CH₂)₇CH₃
CH₃
NH₂
236.363

I-8
(CH₂)₇CH₃
CH₃
SCH₂C(═CH₂)CH₃
307.506

I-9
(CH₂)₇CH₃
CH₃
SCH₂CH═CH₂
293.479

I-10
(CH₂)₇CH₃
CH₃
SCH₂C₆H₅
343.539

I-11
(CH₂)₇CH₃
CH₃
SH
253.414

I-12
(CH₂)₇CH₃
CH₃
SO₂CH₃
299.439

I-13
(CH₂)₇CH₃
CH₃
SO₂CH₂CH═CH₂
325.477

I-14
(CH₂)₇CH₃
CH₃
SO₂CH₂C₆H₅
375.537

I-15
(CH₂)₃C₆H₅
CH₃
SCH₃
273.404

I-16
(CH₂)₇CH₃
CH₃
CH₃
235.375

I-17
(CH₂)₇CH₃
CH₃
OCH₃
251.374

I-18
(CH₂)₃C₆H₅
CH₃
SCH₂CH═CH₂
299.442

I-19
(CH₂)₇CH₃
CH₃
SCH₂CH₃
281.468

I-20
(CH₂)₇CH₃
CH₃
SCH₂CH₂CH₃
295.495

I-21
(CH₂)₇CH₃
CH₃
SCH₂CH₂CH═CH₂
307.506

I-22
(CH₂)₇CH₃
CH₃
S(CH₂)₂OCH₂CH₃
325.521

I-23
(CH₂)₇CH₃
CH₃
S(CH₂)₅CH₃
337.576

I-24
(CH₂)₇CH₃
CH₃
SCH(CH₃)₂
295.495

I-25
(CH₂)₇CH₃
CH₃
S(CH₂)₂OCH₃
311.494

I-26
(CH₂)₇CH₃
CH₃
S(CH₂)₂SCH₂CH₃
341.588

I-27
(CH₂)₇CH₃
CH₃
SCH₂CH═CHCH₃
307.506

I-28
(CH₂)₇CH₃
CH₃

337.532

I-29
(CH₂)₇CH₃
CH₃
SCH₂(4-Cl-C₆H₄)
377.984

I-30
(CH₂)₇CH₃
CH₃
SCH₂(3-Cl-C₆H₄)
377.984

I-31
(CH₂)₈CH₃
CH₃
SCH₃
281.468

I-32
(CH₂)₃CH₃
CH₃
SCH₂CH₃
225.36

I-33
(CH₂)₃CH₃
CH₃
SCH₃
211.333

I-34
(CH₂)₄CH₃
CH₃
SCH₃
225.36

I-35
(CH₂)₅CH₃
CH₃
SCH₃
239.387

I-36
(CH₂)₇CH₃
CH₃
SCH₂CH(CH₃)₂
309.522

I-37
(CH₂)₂CH(CH₃)CH₂C(CH₃)₃
CH₃
SCH₃
281.468

I-38
(CH₂)₃CH₃
CH₃
N(CH₃)₂
208.309

I-39
(CH₂)₇CH₃
CH₃
SCH(CH₃)CH₂OCH₃
325.521

I-40
(CH₂)₇CH₃
CH₃
N(CH₂CH₃)₂
292.471

I-41
(CH₂)₇CH₃
CH₃
C₆H₅
297.446

I-42
(CH₂)₇CH₃
CH₃
SCH₂C(O)NH₂
310.466

I-43
(CH₂)₇CH₃
CH₃
CH(CH₃)₂
263.429

I-44
CH₂CH(CH₂CH₃)(CH₂)₃CH₃
CH₃
SCH₂CH═CH₂
293.479

I-45
CH₂CH(CH₂CH₃)(CH₂)₃CH₃
CH₃
SCH₃
267.441

I-46
(CH₂)₇CH₃
CH₃
pyrrolidin-1-yl
290.455

I-47
(CH₂)₇CH₃
CH₃
N(CH₃)₂
264.417

I-48
(CH₂)₇CH₃
CH₃
N(CH₃)CH₂CH₃
278.444

I-49
(CH₂)₇CH₃
CH₃
CH₂CH₃
249.402

I-50
(CH₂)₇CH₃
CH₃
CH₂CH₂CH₃
263.429

I-51
(CH₂)₇CH₃
CH₃
OCH(CH₃)₂
279.428

I-52
(CH₂)₂CH(CH₃)CH₂C(CH₃)₃
CH₃
N(CH₂CH₃)₂
306.498

I-53
(CH₂)₂CH(CH₃)CH₂C(CH₃)₃
CH₃
CH₃
249.402

I-54
(CH₂)₂CH(CH₃)CH₂C(CH₃)₃
CH₃
OCH₃
265.401

I-55
(CH₂)₂CH(CH₃)CH₂C(CH₃)₃
CH₃
SCH₂CH═CH₂
307.506

I-56
(CH₂)₇CH₃
CH₃
morpholin-1-yl
306.454

I-57
(CH₂)₇CH₃
CH₃

332.536

I-58
(CH₂)₇CH₃
CH₃

318.509

I-59
(CH₂)₇CH₃
CH₃

334.508

I-60
(CH₂)₇CH₃
CH₃
piperidin-1-yl
304.482

I-61
(CH₂)₈CH₃
CH₃
N(CH₃)₂
278.444

I-62
(CH₂)₈CH₃
CH₃
N(CH₂CH₃)₂
306.498

I-63
(CH₂)₇CH₃
CH₃
N(CH₂CH₂CH₃)₂
320.525

I-64
(CH₂)₇CH₃
CH₃
N(CH₃)CH₂CH₂CH₃
306.498

I-65
(CH₂)₇CH₃
CH₃
N(CH₂CH₂CH₂CH₃)₂
348.579

I-66
(CH₂)₈CH₃
CH₃
piperidin-1-yl
318.509

I-67
(CH₂)₈CH₃
CH₃
pyrrolidin-1-yl
304.482

I-68
(CH₂)₈CH₃
CH₃
morpholin-1-yl
320.481

I-69
(CH₂)₂CH(CH₃)CH₂C(CH₃)₃
CH₃
N(CH₃)₂
278.444

I-70
(CH₂)₄CH₃
CH₃
N(CH₃)₂
222.336

I-71
(CH₂)₇CH₃
CH₃

315.465

I-72
(CH₂)₇CH₃
CH₃
pyrazol-1-yl
287.411

I-73
(CH₂)₇CH₃
CH₃
1,2,4-triazol-1-yl
288.399

I-74
(CH₂)₇CH₃
CH₃
Cl¹⁾
511.586

I-75
(CH₂)₇CH₃
CH₃
OCH₂CH₃
265.401

I-76
(CH₂)₂CH(CH₃)CH₂C(CH₃)₃
CH₃
pyrrolidin-1-yl
304.482

I-77
(CH₂)₂CH(CH₃)CH₂C(CH₃)₃
CH₃
piperidin-1-yl
318.509

I-78
CH₂CH(CH₂CH₃)(CH₂)₃CH₃
CH₃
N(CH₃)₂
264.417

I-79
CH₂CH(CH₂CH₃)(CH₂)₃CH₃
CH₃
pyrrolidin-1-yl
290.455

I-80
(CH₂)₉CH₃
CH₃
N(CH₃)₂
292.471

I-81
(CH₂)₉CH₃
CH₃
N(CH₂CH₃)₂
320.525

I-82
(CH₂)₉CH₃
CH₃
pyrrolidin-1-yl
318.509

I-83
(CH₂)₉CH₃
CH₃
piperidin-1-yl
332.536

I-84
—(CH₂)₅—
NH₂
178.239

I-85
—CH₂CH(CH₃)CH(CH₃)CH₂—
NH₂
192.266

I-86
—(CH₂)₄—
NH₂
164.212

I-87
—(CH₂)₃—
(CH₂)₃CN
202.261

I-88
(CH₂)₇CH₃
CH₃
CN
246.358

I-89
(CH₂)₇CH₃
CH₃
C(═NOH)NH₂
279.388

I-90
(CH₂)₇CH₃
CH₃
C(═NOCH₃)NH₂
293.415

I-91
(CH₂)₇CH₃
CH₂CH₃
CN
260.385

#denotes the bond to the pyrimidine ring

¹⁾mixture with 4-chloro-6-methyl-5-octylpyrimidin-2-ylamine

Examples of the Action Against Harmful Fungi

The fungicidal action of the compounds of the formula I was demonstrated by the following experiments:

The active compounds were prepared as a stock solution comprising 25 mg of active compound which was made up to 10 ml using a mixture of acetone and/or DMSO and the emulsifier Uniperol® EL (wetting agent having emulsifying and dispersing action based on ethoxylated alkylphenols) in a volume ratio of solvent:emulsifier of 99:1. The mixture was then made up to 100 ml with water. This stock solution was diluted with the solvent/emulsifier/water mixture described to the concentration of active compounds stated below.

Use Example 1
Activity Against Late Blight of Tomatoes Caused by Phytophthora infestans, Protective Treatment

Leaves of potted tomato plants were sprayed to runoff point with an aqueous suspension having the concentration of active compounds stated below. The next day, the leaves were infected with an aqueous sporangia suspension of Phytophthora infestans. The plants were then placed in a water-vapor-saturated chamber at temperatures between 18 and 20° C. After 6 days, the late blight on the untreated, but infected control plants had developed to such an extent that the infection could be determined visually in %.

In this test, the plants which had been treated with 250 ppm of the compounds I-2, I-4, I-35, I-41 to 46, I-48, I-51 to 55, I-57 to 60, I-62 to 65, I-68, I-71, I-73, I-74, I-79, I-88 or I-91 showed at most 20% infection, whereas the untreated plants were 85-90% infected.

Use Example 2
Activity Against the Late Blight Pathogen Phytophthora infestans in the Microtiter Test

50 μl of the required concentration of active compounds were pipetted onto a microtiter plate (MTP). The plate was then inoculated with 50 μl of an aqueous sporangia suspension of Phytophthora infestans. The plates were placed in a water-vapor-saturated chamber at temperatures of 18° C. On the seventh day after the inoculation, the absorption of the MTPs was measured at 405 nm using an absorption photometer. Using the measured parameters, the growth of the control and the blank value, the relative growth in % of the pathogens in the individual active compounds was determined.

In this test, at 125 ppm of the compound I-3 or I-4, the relative growth found was at most 11%.

Use Example 3
Protective Activity Against Rice Blast Caused by Pyricularia oryzae in the Microtiter Test

50 μl of the required concentration of active compounds were pipetted onto a microtiter plate (MTP). The plate was then inoculated with 50 μl of an aqueous sporangia suspension of Pyricularia oryzae. The plates were placed in a water-vapor-saturated chamber at temperatures of 18° C. On the seventh day after the inoculation, the absorption of the MTPs was measured at 405 nm using an absorption photometer. Using the measured parameters, the growth of the control and the blank value, the relative growth in % of the pathogens in the individual active compounds was determined. In this test, at 125 ppm of the compound I-3 growth was inhibited completely.

Use Example 4
Activity Against peronospora of Grapevines Caused by Plasmopara viticola, 7 Day Protective Treatment

Leaves of potted vines were sprayed to runoff point with an aqueous suspension having the concentration of active compounds stated below. To be able to assess the persistency of the substances, the plants were, after the spray coating had dried on, placed in a greenhouse for 7 days. Only then were the leaves inoculated with an aqueous zoospore suspension of Plasmopara viticola. The vines were then initially placed in a water vapor-saturated chamber at 24° C. for 24 hours and then in a greenhouse at temperatures between 20 and 30° C. for 5 days. After this time, the plants were once more placed in a humid chamber for 16 hours to accelerate the eruption of sporangiospores. The extent of the development of the infection on the undersides of the leaves was then determined visually.

In this test, the plants which had been treated with 500 ppm of the compounds I-1, I-2, I-4, I-10 to 14, I-16, I-17, I-20, I-22, I-23, I-26, I-27, I-28, I-33, I-35 to 53, I-55 to 66, I-68, I-70, I-72 to I-79, bzw. I-80 showed an infection of at most 15%, whereas the untreated plants were 75% infected.

Use of 4-Aminopyrimidines for Controlling Harmful Fungi, Novel 4-Aminopyrimidines, Processes for Their Preparation and Compositions Comprising Them

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