Abstract:
The present invention relates to mixtures of fungicidally active compounds comprising at least one substituted 2-[hydroxyl(pyridine-3-yl)methyl]acrylate compound of the formula (I) wherein: R 1 is H, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl,C 1 -C 6 -haloalkyl, aryl or het- eroaryl, wherein the cyclic moieties of the last two radicals are unsubsti- tuted or substituted with 1, 2 or 3 radicals selected from halogen, C 1 -C 4 alkyl, C 2 -C 4 -alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 - haloalkoxy, cyano and nitro; A is a covalent bond or C 1 -C 4 -alkylen, which is unsubstituted or which may carry a substitutent selected from C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy and cyano; Ar is aryl or heteroaryl, wherein the cyclic moieties of the aromatic radicals are unsubstituted or substituted with 1, 2 or 3 radicals Ra, where the radicals Ra are identical or different and selected from halogen, C 1 -C 4 -alkyl, C 2 -C 4 - alkenyl, C 2 -C 4 -alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 - C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano, nitro, aryl, hetaryl, aryloxy, hetaryloxy, aryloxy-C 1 -C 4 -alkyl and hetaryloxy-C 1 -C 4 -alkyl, wherein the cyclic moieties of the six last mentioned radicals are unsubstituted or substi- tuted with 1, 2 or 3 radicals selected from halogen, C 1 -C 4 -alkyl, C 1 -C 4 - haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, cyano and nitro; or a salt thereof; and at least one further fungicidally active compound II.
Abstract:
The invention relates to thiazole carboxylic acid anilides of formula (I), in which the variables are defined as follows: X represents halogen; Y represents cyano, nitro, C1-C4-alkyl, C1-C4 haloalkyl, methoxy or methylthio; p represents 0.1; R1 represents hydrogen, halogen, C1-C4 alkyl or C1-C4 haloalkyl; R2 represents hydrogen, methyl or halogen; R3 represents hydrogen, methyl or ethyl; W represents O or S. The invention also relates to a method for producing said compounds, to agents containing the latter, to seed and to a method for controlling pathogenic fungi.
Abstract:
The present invention relates to compounds of the formula (I) and the use thereof for combating phytopathogenic fungi, and to fungicidal mixtures comprising a compound of the formula (I), wherein the variables and substituents are as defined in the claims and the description.
Abstract:
The invention relates to pyridazines of the formula (I), in which the substituents are defined according to the description, methods and intermediate products for the production of said compounds, agents containing the same and the use thereof for controlling plant-pathogenic fungi, and the use of pyridazines for the production of a drug for the treatment of cancer.
Abstract:
The invention relates to azolylmethyloxiranes of general formula (I), wherein A or B represent a 5-membered heteroaryl, selected from thienyl, furyl, pyrrolyl, paryzolyl, imidazolyl, oxazolyl, thiazolyl, isoxazolyl and isothiazolyl, which is substituted by one to three of the following substituents: halogen, NO2, amine, C1- C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy, C1-C4 alkylamino, C1-C4 dialkylamino, thio or C1-C4 alkylthio, and the respective other substituent A or B represents phenyl which is optionally substituted by one to three of the following substituents: halogen, NO2, amine, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1- C4 halogenalkoxy, C1-C4 alkylamino, C1-C4 dialkylamino, thio or C1-C4 alkylthio, and to the acid addition or metal salts thereof that are tolerated by plants. The invention also relates to the use of the compounds of formula I for controlling phytopathogenic fungi and to agents containing said compounds.
Abstract:
The invention relates to azolylmethyloxiranes of general formula (I), wherein A or B represent a 6-membered heteroaryl, selected from pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl and triazinyl, which is substituted by one to three of the following substituents: halogen, NO2, amine, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy, C1-C4 alkylamino, C1-C4 dialkylamino, thio or C1-C4 alkylthio, and the respective other substituent A or B represents phenyl which is optionally substituted by one to three of the following substituents: halogen, NO2, amine, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy, C1-C4 alkylamino, C1-C4 dialkylamino, thio or C1-C4 alkylthio, and to the acid addition or metal salts thereof that are tolerated by plants. The invention also relates to the use of the compounds of formula (I) for controlling phytopathogenic fungi and to agents containing said compounds.
Abstract:
The present invention relates to azolylmethyloxiranes of the general formula I, in which A is phenyl substituted by two F, B is unsubstituted pyridyl, thienyl, thiazolyl, oxazolyl or furyl, or is phenyl substituted by from one to three of the following substituents: halogen, NO2, amino, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylamino, C1-C4-dialkylamino, thio or C1-C4-alkylthio, with the proviso that B is not o-methylphenyl when A is 2,4-difluoro-phenyl, and to their acid addition or metal salts compatible with plants, to the use of the compounds of the formula I for controlling phytopathogenic fungi and to compositions comprising them.
Abstract:
The invention relates to 3-(pyridin-2-yl)-[1,2,4]-triazines of formula (I) and their use in the control of parasitic fungi and to herbicides that contain said compounds as an effective ingredient thereof. In formula (I), R1, R2 independently represent OH, halogen, NO2, NH2, C1-C8 alkyl, C1-C8 alkoxy, C1-C8 halogenalkyl, C1-C8 halogenalkoxy, C1-C8 alkylamino or di(C1-C8 alkyl)amino, or they form, together with the C atoms to which they are bound, a saturated five-, six- or seven-membered carbocycle or heterocycle, which, in addition to the carbon ring members, has one or two heteroatoms selected from oxygen or sulfur as the ring members, the carbocycle and the heterocycle being unsubstituted or having 1, 2, 3 or 4 C1-C4 alkyl groups as the substituents; R3 represents hydrogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy, C3-C6 cycloalkyl, C3-C6 cycloalkylmethyl, or halogen; R4 represents hydrogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy or halogen; R5 represents C1-C8 alkyl, C1-C8 halogenalkyl, C1-C8 alkoxy, C1-C8 halogenalkoxy, C3-C8 cycloalkyl, C3-C8 cycloalkyloxy, five- or six-membered heteroaryl, phenyl, phenoxy, benzyl, benzyloxy, five- or six-membered heteroarylmethyl or five- or six-membered heteroaryloxy, said cyclic groups being unsubstituted or having 1, 2, 3, 4 or 5 groups Ra.
Abstract:
The present invention relates to the use as fungicides of 2-substituted pyrimidines of the formula (I) in which the substituents are as defined in the description, to new pyrimidines, to processes and intermediates for their preparation, and to compositions comprising them.
Abstract:
5-Alkyl-6-phenylpyrazolopyrimidin-7-ylamines of the formula (I) in which the substituents are defined as in the description, processes for preparing these compounds, compositions comprising them, and their use for controlling phytopathogenic fungi.