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 present invention relates to novel biphenyl-4-sulfonicacid (quinolin-4-ylmethyl)- amide compounds of formula (I) wherein R 1 and R 2 are halogen, OH, CN, NH 2 , NO 2 , C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 3 -C 7 -cycloalkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkyl, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -alkylsulfinyl, C 1 -C 6 -alkylsulfonyl, etc.; R 3 , R 4 , R 5 , R 6 are halogen, H, CN, NH 2 , NO 2 , OH, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkyl, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -alkylsulfinyl, C 1 -C 6 -alkylsulfonyl, etc.; m is 0, 1, 2, 3, 4, or 5; and n is 1 or 2; and the N-oxides and salts thereof, and their use for combating arthropod pests and nematodes, and also to compositions comprising such compounds as active component. The present invention also relates to a method for controlling arthropod pests or nematode pests.
Abstract:
The present invention relates to thiophene-sulfonic acid picolyl amides of the Formula (I), where R 1 to R 7 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, R 6 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:
Die vorliegende Erfindung betrifft Azolopyrimidine der Formel I in der die Substituenten gemäß der Beschreibung definiert sind, Verfahren und Zwischenprodukte zur Herstellung dieser Verbindungen, sie enthaltende Mittel sowie ihre Verwendung zur Bekämpfung von pflanzenpathogenen Schadpilzen.
Abstract:
Disclosed are compounds of formula (I), wherein X, Y, and Z are defined as indicated in the description, methods and intermediate products for producing said compounds, substances containing the same, and the use thereof for controlling plant pathogenic fungi.
Abstract:
Die vorliegende Erfindung betrifft substituierte Triazolopyrimidine der Formel (I) in der die Substituenten die Bedeutungen besitzen, wie sie in der Beschreibung definiert sind.
Abstract:
Substituierte Pyrazolopyrimidine der Formel (I), in der die Substituenten gemäß der Beschreibung definiert sind, und landwirtschaftlich annehmbare Salze davon, Verfahren und Zwischenprodukte zur Herstellung dieser Verbindungen, sie enthaltende Mittel sowie ihre Verwendung zur Bekämpfung von pflanzenpathogenen Schadpilzen.
Abstract:
The present invention relates to pyridin-4-ylmethylamides of the general formula (I), where R 1 to R 6 and n are as defined in the claims and to the N-oxides and the agriculturally acceptable salts of the compounds I. 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). Furthermore the compounds I, their N-oxides and salts can be used for controlling arthropodal pests.
Abstract:
N-[2-(Haloalkoxy)phenyl]heteroarylcarboxamides of the formula I, where n = 0 or 1, Hal = halogen, X = C 2 -C 4 -haloalkyl, Het = a pyrazole, thiazole or pyridine radical (a), (b) or (c), where R 1 = C 1 -C 4 -alkyl or C 1 -C 4 -haloalkyl, R 2 = hydrogen or halogen, R 3 = C 1 -C 4 -alkyl or C 1 -C 4 -haloalkyl and R 5 = halogen, C 1 -C 4 -alkyl or C 1 -C 4 -haloalkyl; except for N-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-1,3-dimethylpyrazol-4-yl-carbox-amide, N-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]-3-trifluoromethyl-1-methylpyrazol-4-yl- carboxamide and N-[2-(2,2,2-trifluorethoxy)phenyl]-3-trifluormethyl-1-methylpyrazol-4-yl-carboxamide. A fungicidal composition comprising at least one compound I, the use of the compounds I for preparing a composition suitable for controlling harmful fungi, a method for controlling harmful fungi using the compounds I and also seed comprising at least one compound I.
Abstract:
5-Methyl-6-phenyl-triazolopyrimidinylamine der Formel (I), in der die Substituenten gemaβ der Beschreibung definiert sind, Verfahren zur Herstellung dieser Verbindungen, sie enthaltende Mittel sowie ihre Verwendung zur Bekampfung von pflanzenpathogenen Schadpilzen.