Abstract:
The present invention relates to novel triazole compounds of the formulae (I), (II) and (IV) as defined below, to agricultural and pharmaceutical compositions containing them and to their use as fungicides, antimycotic, anticancer and antiviral agents.
Abstract:
The invention relates to azolylmethyloxiranes of general formula (I), wherein A or B is benzodioxolyl which is optionally substituted by between one and five of the following substituents, halogen, CN, NO2, amino, 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 is phenyl or 5-membered or 6-membered heteroaryl, said substituents being optionally substituted by between one and three of the following substituents, halogen, CN, NO2, amino, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy, C1-C4 alkylamino, C1-C4 dialkylamino, thio or C1-C4 alkylthio. The invention also relates to the plant-tolerant acid addition salts or metal salts of said compounds, to the use of the compounds of formula (I) for controlling plant-pathogenic fungi, and to agents containing the same.
Abstract:
The invention relates to compounds of formula (I) wherein the variables have the designations defined in the claims and in the description, and to the use thereof as fungicides or in an antimycotic agent.
Abstract:
The present invention relates to compounds of formula (I), wherein the variables have the meanings defined in the claims and the description.
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 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.