Abstract:
The present invention relates to compounds of formula (I), wherein the variables have the meanings defined in the claims and the specification, and use thereof as fungicides and in an antimycotic agent.
Abstract:
The present invention relates to pyridin-4-ylmethyl sulfonamides of formula I wherein R a , n, R, A and Het are as defined in the claims, to the N-oxides, and salts thereof and their use for combating harmful fungi, and also to compositions and seed comprising at least one such compound. The invention also relates to a process and intermediates for preparing these compounds.
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 triazinylmethyl sulfonamides of formula (I): wherein T, R 1 , R 2 , R 3 , A, Y and D are as defined in the claims and to the N-oxides, and salts thereof and their use for combating harmful fungi, and also to compositions and seed comprising at least one such compound. The invention also relates to processes and intermediates for preparing these compounds.
Abstract:
The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R1 represents alkyl, alkoxymethylene or alkoxyethylene, whereby the aliphatic groups can be substituted according to the description and R2 represents n-propyl or n-butyl. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.
Abstract:
The present invention relates to novel pyrimidylmethyl-sulfonamide compounds of formula (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 invention relates to the use of benzophenones of general formula (I), in which R represents hydrogen or C1-C4 alkyl while Hal represents fluoride, chlorine, or bromine, for controlling Pseudocercosporella herpotrichoides in cultivated plants.
Abstract:
The present invention relates to the use of 5-hetaryl-4-aminopyrimidines of the formula I and of their salts for controlling phytopathogenic fungi. The invention also relates to novel 5-hetaryl-4-aminopyrimidines and to plant protection compositions which contain at least one such compound as active component. Het represents an optionally substituted 5- or 6-membered aromatic heterocycle which has 1, 2, 3 or 4 hetero atoms as ring members which are selected among nitrogen, oxygen and sulphur, where the 5- or 6-membered heteroaromatic radical can have 1, 2, 3 or 4 identical or different substituents L; R1, R2 represent inter alia hydrogen, C1-C8-alkyl, C3-C8-cycloalkyl, C5-C10-bicycloalkyl, C2-C8-alkenyl, C4-C10-alkadienyl, C3-C6-cycloalkenyl, C2-C8-alkynyl, phenyl, naphthyl or a five- or six-membered saturated, partially unsaturated or aromatic heterocycle which has one, two, three or four hetero atoms from the series O, N or S as ring members; or together form a ring; R3 represents, inter alia, hydrogen, OH, halogen, cyano, NR31R32, C1-C8-alkyl, C1-C8-alkoxy, C1-C8-alkylthio, C1-C8-alkylsulphinyl, C1-C8-alkyl-sulphonyl, C2-C8-alkenyl or C2-C8-alkynyl; and R4 represents halogen, cyano, hydroxy, mercapto, N3, C1-C6-alkyl, C2-C8-alkenyl, C2-C8-alkynyl, C1-C6-haloalkyl, C1-C6-alkoxy, C3-C8-alkenyloxy, C3-C8-alkynyloxy, C1-C6-haloalkoxy, C1-C6-alkylthio, C3-C8-alkenylthio, C3-C8-alkynylthio, C1-C6-haloalkylthio, or represents a radical of the formulae C(=Z)OR41, C(=Z)NR42R43, C(=Z)NR44-NR42R43, C(=Z)R45, CR46R47-OR48, CR46R47-NR42R43, ON(=CR49R50), O-C(=Z)R45, NR42R43a, NR51(C(=Z)R45), NR51(C(=Z)OR41), NR51(C(=Z)-NR42R43), NR52a(N=CR49R50), NR52NR42R43, NR52OR41, or C(=N-X-R45)SR41.
Abstract:
The invention relates to 5-alkoxyalkyl-6-alkyl-7-amino-azolopyrimidines of formula (I), in which the substituents are defined as follows: R1 represents alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, cyanoalkyl and benzyloxyalkyl, the groups in the aliphatic or aromatic part being unsubstituted or substituted by one to three groups Ra, where the latter represents halogen, cyano, nitro, hydroxy, cycloalkyl, alkoxy, alkylthio and NRARB, (RA and RB representing hydrogen and alkyl; R2 represents alkoxyalkyl, phenoxyalkyl, alkylthioalkyl and phenylthioalkyl, said groups being unsubstituted or substituted according to the description; R3 represents hydrogen and alkyl; A represents N and C-RA. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.