Abstract:
Die vorliegende Erfindung betrifft Verbindungen der Formel (I) und deren Verwendung zur Bekämpfung phytopathogener Pilze, wobei die Variablen und Substituenten die Bedeutungen besitzen, wie sie in den Ansprüchen und der Beschreibung definiert sind.
Abstract:
Verwendung von substituierten Triazolopyrimidinen der Formel (I), in der die Substituenten gemäß der Beschreibung definiert sind, zur Bekämpfung von Schadpilzen, neue Triazolopyrimidine, Verfahren und Zwischenprodukte zu ihrer Herstellung sowie sie enthaltende Mittel.
Abstract:
Oximether compounds of formula (I) wherein A is selected from A 1 and A 2 ; E is O or S(=O) r ; r is 0, 1 or 2; X is C-Y or N; Y is halogen, CN, NO 2 , NH 2 , OH, SH, R 1 , OR 1 , SR 1 , S(=O)R 1 , S(=O) 2 R 1 , NHR 1 , NR 1 R 2 , C(=O)H, C(=O)R 1 , C(=O)OH, C(=O)OR 1 , C(=O)NHR 1 , C(=O)NR 1 R 2 , C(=S)R 1 , C(=S)OR 1 , C(=S)NHR 1 , C(=S)NR 1 R 2 , OC(=O)R 1 , OC(=S)R 1 , NHC(=O)R 1 , NR 1 C(=O)R 2 , NHC(=O)OR 1 , NR 1 C(=O)OR 2 , NHC(=S)R 1 , NR 1 C(=S)R 2 , NHC(=S)OR 1 , NR 1 C(=S)OR 2 , N[C(=O)R 1 ] 2 , C(=O)NR 1 -NR 2 R 3 , C(=O)NH- NR 1 R 2 , C(=O)NH-NHR 1 , C(=O)NR 1 -NHR 2 , C(=O)NH-NH 2 , NR 1 -N[C(=O)R 2 ] 2 , N[C(=S)R 1 ] 2 , C(=S)NR 1 -NNR 2 R 3 , NR 1 -N[C(=S)R 2 ] 2 , O-NR 2 R 3 , -O-NHR 1 , -SO 2 NHR 1 , SO 2 NR 1 R 2 , NHSO 2 R 1 , NR 1 SO 2 R 2 , SiR 1 3 , P(=O)R 1 2 , P(=S)R 1 2 ; or an optionally substituted 5- to 6-membered heteroaromatic ring which contains 1 to 3 heteroatoms selected from O, N and S; R 1 , R 2 and R 3 are optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or phenyl; Q and W are Y or NR 3 C(=O)NR 1 R 2 , NR 3 C(=S)NR 1 R 2 or NHC(=O)R 1 ; Z is Y or NR 3 C(=O)NR 1 R 2 or NR 3 C(=S)NR 1 R2; m is 0, 1, 2, 3 or 4; n is 0, 1, 2, or 3; o, p and q are 0, 1, 2, 3, 4 or 5; with the exemption of 1-{4- [4-(trifluoromethyl)phenoxy]phenyl}-O-{[2,6-dichloro-4-[(3,3-dichloro-2- propenyl)oxy]phenyl]methyl]oxime ethanone, processes for preparing compounds I, pesticidal compositions comprising compounds I and use of compounds I for the control of pests and parasites.
Abstract:
Biphenylsulfonamides of the formula (I) and the N-oxides and the agriculturally acceptable salts and the veterinarily acceptable salts of the compounds I, a process for preparing these compounds, compositions comprising them, their use for controlling phytopathogenic harmful fungi and harmful arthropodes, a method for combating arthropodal pests, a method for protecting crops from attack or infestation of arthropodal pests, a method for protecting seed and non-living materials from infestation by arthropodal pests, a method for protecting non-living materials from attack or infestation by arthropodal pests and seed comprising the compounds I.
Abstract:
N-(4-Pyridyl)methylsulfonamides for combating arthropodal pests The present invention relates to the use of N-(4-pyridyl)methylsulfonamides of the formula for combating arthropodal pests (harmful arthropodes) and for protecting materials against infestation and/or destruction by said pests: (I) where the substituents are as follows: R 1 is hydrogen, C 1 -C 4 -alkyl, C 1- C 4 -alkoxy, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl or benzyl; R 2 , R 3 , R 4 , R 5 independently of one another are hydrogen, halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkoxy or C 1 -C 4 -haloalkyl; R 2 and R 3 or R 4 and R 5 together with the carbon atoms to which they are attached may also form a condensed 5- or 6-membered hydro- carbon ring, it being possible for the hydrocarbon ring to carry one or two groups R 2' , R 3' , R 2' , R 3' independently of one another are halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, halomethoxy or halomethyl; X is a cyclic radical selected from phenyl, naphthyl and five- or six-membered saturated, partially unsaturated or aromatic heterocycles, the heterocycle being attached to the sulfur atom via a carbon atom and containing 1 , 2 or 4 heteroatoms selected from the group consisting of O, N and S, where the cyclic radical X may carry 1 , 2, 3 or 4 substituents R a .
Abstract:
2-Substituierte 7-Amino-azolopyrimidine der Formel (I) in der die Substituenten folgende Bedeutung haben: R 1 Wasserstoff, Halogen, Cyano, Alkyl, Halogenalkyl, Alkenyl, Alkinyl, Cycloalkyl, Alkoxy, Alkoxyalkyl, Benzyloxyalkyl, Alkoxyalkenyl oder Alkoxyalkinyl; R 2 Wasserstoff, Halogen, Cyano, Alkyl, Halogenalkyl, Alkenyl, Alkinyl, Cycloalkyl, Alkoxy, Alkoxyalkyl und Alkylthioalkyl, wobei die Kohlenstoffketten in R 1 und/oder R 2 gemäß der Beschreibung substituiert sein können; R 3 Halogen, Cyano, NR A R B , Hydroxy, Mercapto, Alkyl, Halogenalkyl, Cycloalkyl, Alkoxy, Alkylthio, Cycloalkoxy, Cycloalkylthio, Carboxyl, Formyl, Alkylcarbonyl, Alkoxycarbonyl, Alkenyloxycarbonyl, Alkinyloxycarbonyl, Phenyl, Phenoxy, Phe- nylthio, Benzyloxy, Benzylthio, Alkyl-S(O) m- ; A N und CR x ; R x Wasserstoff oder eine der bei R 3 genannten Gruppen; Verfahren und Zwischenprodukte zur Herstellung dieser Verbindungen, sie enthaltende Mittel sowie ihre Verwendung zur Bekämpfung von pflanzenpathogenen Schadpilzen.
Abstract:
The invention relates to 2-substituted 7-amino-azolopyrimidine of formula (I), wherein substituents have the following meanings: R 1 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, Cycloalkyl, alkoxy, alkoxyalkyl, benzyloxyalkyl, alkoxyalkenyl or akoxyalkinyl; R 2 is hydrogen, halogen, cyano, alkyl, halogenalkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkoxyalkyl and alkylthioalkyl, wherein a carbon chain in R 1 and/or R 2 are substitutable according to a description; R 3 is halogen, Cyano, NR A R B , hydroxy, mercapto, alkyl, halogenalkyl, cycloalkyl, alkoxy, alkylthio, cycloalkoxy, cycloalkylthio, carboxyl, formyl, alkylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, phenyl, phenoxy, phe- nylthio, benzyloxy, benzylthio, alkyl-S(O) m- ; A N and CR x ; R x is hydrogen or one of above groups for R 3 . A method and intermediate products for producing said compounds, agents containing said compounds and the use thereof for combating plant-pathogen fungi are also disclosed.
Abstract translation:2-取代的式(I)其中取代基具有以下含义的7-氨基azolopyrimidines:R t 1 SUP>为氢,卤素,氰基,烷基,卤代烷基,烯基,炔基,环烷基,烷氧基,烷氧基烷基, benzyloxyalkyl,烷氧基烯基或alkoxyalkynyl; [R 2 SUP>为氢,卤素,氰基,烷基,卤代烷基,烯基,炔基,环烷基,烷氧基,烷氧基烷基和烷硫基烷基,其中在R中的碳链 1 SUP>和/或R 2 SUP>可以根据描述被取代; [R 3 SUP>为卤素,氰基,NR 一 SUP> - [R 乙 SUP>,羟基,巯基,烷基,卤代烷基,环烷基,烷氧基,烷硫基,环烷氧基,环烷硫基, 羧基,甲酰基,烷基羰基,烷氧基羰基,烯氧基羰基,炔氧基羰基,苯基,苯氧基,苯丙氨酸nylthio,苄氧基,苄硫基,烷基-S(O)米 - SUB>; A N和CR X SUP>; ,R 3 SUP>基 X SUP>是氢或其中R 称作; 的方法和中间体制备这些化合物,含有它们和它们在防治植物病原性有害真菌的组合物。
Abstract:
Die vorliegende Erfindung betrifft 1-Methyl-3-trifluormethyl-pyrazol-4-carbonsäure-(ortho-phenyl)-anilide der Formel I in der die Substituenten die folgende Bedeutung haben: R1 und R 2 unabhängig voneinander Halogen, C1-C6-Alkyl, C1-C6 Halogen-alkyl, Cyano, Nitro, Methoxy, Trifluormethoxy oder Difluormethoxy; mit der Maßgabe, dass, wenn R2 in der 4-Position Chlor bedeutet, R1 in der 3-Position nicht für Trifluormethyl steht.
Abstract:
The invention relates to 6-(2,6-dichlorophenyl)-triazolopyrimidines of formula (I) wherein the substituents have the following designations: R and R represent hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, halogencycloalkenyl, alkinyl, halogenalkinyl or phenyl, naphthyl, or a five-membered or six-membered saturated, partially unsaturated or aromatic heterocycle containing between one and four heteroatoms from the group containing O, N or S; R and R can also form, together with the nitrogen atom to which they are bound, a five-membered or six-membered heterocycle or heteroaryl which is bound by N and contains between one and three other heteroatoms from the group containing O, N and S as a cyclic member and is substituted according to the description; and X represents alkyl, cyano, alkoxy, halogenalkoxy, alkenyloxy or halogenalkenyloxy, but does not represent C1-C4 alkyl when R and R together represent piperidin-1-yl or 4-methylpiperidin-1-yl. The invention also relates to a method for producing said compounds, agents containing the same, and the use thereof for controlling plant pathogenic fungi.