Abstract:
The present invention relates to a new process for the preparation of substituted thio-triazolo groups of the general formula (I) wherein the variables have the meanings as given in the claims and the description.
Abstract:
The invention relates to compounds of formula (I), wherein the variables have the meanings indicated in the claims or the description, and to their agriculturally acceptable salts.
Abstract:
The present invention relates to compounds of the formula, in which the variables have the meanings defined in the claims and the specification.
Abstract:
The present invention relates to azolylmethyloxiranes of the general formula I, in which A is phenyl substituted by one F and a further substituent selected from Cl, C1-C4-alkyl, C1-C4-haloalkyl and C1-C4-alkoxy, 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-chloro-4-fluorophenyl, 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 the triazolylmethyloxiranes of formula (I), wherein variables A, B and D have the meanings as defined in the description and the claims.
Abstract:
The present invention relates to novel pyridazin- 4 -ylmethyl- sulfonamide compounds (I) and to their N-oxides, their agriculturally acceptable salts and their veterinarily acceptable salts and also to agricultural compositions comprising at least one such compound as active component, and also to their use for controlling harmful fungi. The present invention also relates to a method for controlling arthropod pests.
Abstract:
The present invention relates to thiophene-sulfonic acid picolyl amides of the Formula (I), where R1 to R7 and n are as defined in the claims and to the N-oxides, the agriculturally acceptable salts and the veterinarily acceptable salts of the compounds (I), with the proviso that if the thiophene ring is bonded to the sulfonyl group via position 2, R6 cannot be at position 5. The invention also relates to a process for preparing these compounds. Furthermore, the invention relates to the use of the compounds I and the N-oxides and the agriculturally acceptable salts thereof for combating phytopathogenic fungi (hereinafter referred to as harmful fungi). Additionally, the compounds (I), their N-oxides and salts can be used for controlling arthropodal pests. Furthermore, the invention relates to seed comprising a compound (I) or an N-oxide or agriculturally acceptable salt thereof.
Abstract:
The present invention relates to the use of pyrimidine compounds of formula (I), wherein the variables have the meaning stated in the claims and in the description, for combating pathogenic fungi, new pyrimidine compounds of formula (I), and fungicides and pharmaceutical agents containing the same.
Abstract:
The invention relates to 6-phenyl-triazolopyrimidinyl amines of formula (I) wherein the substituents have the designations cited in the description. The invention also relates to methods for producing said compounds, to agents containing the same, and to the use thereof for controlling plant pathogenic fungi.