Abstract:
The invention relates to sulfoximinamid compounds of formula (I), to the enantiomers, diastereomers and salts thereof and to compositions comprising such compounds. The invention also relates to the use of the sulfoximinamid compounds, of their salts or of compositions comprising them for combating animal pests. Furthermore the invention relates also to methods of applying such sulfoximine compounds. The sulfoximinamid compounds of the present invention are defined by the following formula I: wherein Q, Het, R 1 , R 2 , R 3 , R 4 and n are defined as in the description.
Abstract:
The present invention relates to pesticidal mixtures comprising as active components 1) one sulfonamide compound of the formula (I) wherein R 1 , R 2 , R 3 and R 4 are defined as in the description; and 2) one or more fungicidal compounds Il selected from azoles, strobilurins, carboxamides, carbamates, heterocyclic and various other compounds as defined in the description, in synergistically effective amounts. The invention relates further to methods and use of these mixtures for combating insects, arachnids or nematodes and harmful fungis in and on plants, and for protecting such plants being infested with pests, especially also for protecting seeds.
Abstract:
The invention provides 3-amino-1,2-benzisothiazole compounds of formula (I) wherein n, R 1 , R 2 , R 3 , R 4 and A are defined as in the description. The invention provides further agricultural compositions comprising an amount of at least one compound of the formula (I) or an enantiomer, diasteromer or salt thereof; the use of a compound of formula (I) or an enantiomer, diasteromer or salt thereof for combating animal pests; a method of combating animal pests which comprises contacting the animal pests, their habit, breeding ground, food supply, plant, seed, soil, area, material or environment in which the animal pests are growing or may grow, or the materials, plants, seeds, soils, surfaces or spaces to be protected from animal attack or infestation with a pesticidally effective amount of at least one compound of the formula (I) or an enantiomer, diasteromer or salt thereof; a method for protecting crops from attack or infestation by animal pests, which comprises contacting a crop with a pesticidally effective amount of at least one compound of the formula (I) or an enantiomer, diasteromer or salt thereof; a method for the protection of seeds from soil insects and of the seedlings' roots and shoots from soil and foliar insects comprising contacting the seeds before sowing and/or after pregermination with at least one compound of the formula (I), or the enantiomers, diastereomers or salts thereof; and seeds comprising a compound of the formula I or an enantiomer, diasteromer or salt thereof.
Abstract:
The present invention relates to thioamide compounds of the general formula (I) and to the agriculturally useful salts thereof and to compositions comprising such compounds. The invention also relates to the use of the thioamide compounds, of their salts or of compositions comprising them for combating animal pests. wherein R 1 ,R 2 , R 3 ,R 4 ,R 6 and X are defined as in the description.
Abstract:
The invention relates to insecticidal methods using 3-amino-1,2-benzoisothiazole compounds of the formula (I) wherein the variables n and R 1 to R 6 are as defined in the description. The invention relates to methods of combating or controlling insects, arachnids or nematodes, to methods for protecting growing plants from attack or infestation by insects, arachnids or nematodes, and to methods for the protection of seeds from soil insects and of the seedlings' roots and shoots from soil and foliar insects.
Abstract:
The present invention relates to new pyridine compounds which are useful for combating animal pests, in particular insects, arachnids and nematodes. The invention also relates to a method for combating insects, nematodes and arachnids. The pyridine compounds have the formula I as defined below. Likewise, compounds of the formula Il are suitable for combating pests. In formulae I and Il n is 1 or 2, and R1, R2, R3, R4 and R5 are as defined in the claims and in the specification.
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:
Use of compounds of formula (I) wherein Q is (II), (III), or (IV) ; X 1 is chlorine, bromine, or fluorine; R 1 , R 2 are each independently H, alkyl, alkenyl, alkynyl, or cycloalkyl, alkylamino, dialkylamino, alkylcarbonylamino, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, or R 1 and R 2 may be taken together to form a ring represented by the structure (V); p,m are 1, 2 or 3; X' is oxygen, sulfur, amino, alkylamino, phenylamino, or methylene; Z is alkyl or phenyl; R 3 is H, alkyl, alkenyl, alkynyl, cycloalkyl, wherein the carbon atoms in these groups may be substituted; R, R 4 are H or alkyl, alkoxycarbonyl, alkylaminocarbonyl, or dialkylaminocarbonyl, wherein the carbon atoms in the these groups may be substituted; A is C-R 5 or N; B is C-R 6 or N; W is C-R 7 or N; with the proviso that one of A, B and W is other than N; R 5 , R 6 , R 7 are H, halogen, nitro, cyano, amino, mercapto, hydroxy, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted, a 5- to 6-membered aromatic ringsystem which may contain 1 to 4 heteroatoms selected from oxygen, sulfur and nitrogen and which may be substituted; Y is hydrogen, halogen, cyano, nitro, amino, hydroxy, mercapto, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkylsulfonyl, or alkylsulfinyl, wherein the carbon atoms in these groups may be substituted; n is 0, 1, or 2; for combating parasites in and on animals.
Abstract translation:其中Q是(II),(III)或(IV)的式(I)化合物的用途; X 1是氯,溴或氟; R 1,R 2各自独立地为H,烷基,烯基,炔基或环烷基,烷基氨基,二烷基氨基,烷基羰基氨基,烷基磺酰基或烷基亚磺酰基,其中这些中的碳原子 基团可以被取代,或者R 1和R 2可以一起形成由结构(V)表示的环; p,m是1,2或3; X'是氧,硫,氨基,烷基氨基,苯基氨基或亚甲基; Z是烷基或苯基; R 3是H,烷基,烯基,炔基,环烷基,其中这些基团中的碳原子可以被取代; R,R 4为H或烷基,烷氧基羰基,烷基氨基羰基或二烷基氨基羰基,其中这些基团中的碳原子可以被取代; A是C-R 5或N; B是C-R 6或N; W是C-R 7或N; 条件是A,B和W中的一个不是N; R 5,R 6,R 7为H,卤素,硝基,氰基,氨基,巯基,羟基,烷基,链烯基,炔基, 环烷基,烷氧基,烷基氨基,二烷基氨基,烷硫基,烷基磺酰基或烷基亚磺酰基,其中这些基团中的碳原子可被取代,可含有1-4个选自氧,硫和氮的杂原子的5-6元芳族环体系和 它可以被替代; Y是氢,卤素,氰基,硝基,氨基,羟基,巯基,烷基,烯基,炔基,环烷基,烷氧基,烷基氨基,二烷基氨基,烷硫基,烷基磺酰基或烷基亚磺酰基,其中这些基团中的碳原子可以被取代; n是0,1或2; 打击动物体内和体内的寄生虫。 p>
Abstract:
Die vorliegende Erfindung betrifft pyrazolylsubstituierte Thienyloxy-Pyridine der Formel I, in der die Variablen die folgenden Bedeutungen haben: R 1 , R 3 : Wasserstoff, Halogen, Cyano, Nitro, Alkyl, Halogenalkyl, Alkoxy oder Halogenalkoxy; R 2 : Wasserstoff, Halogen, Cyano, Alkenyl, Alkinyl, Halogenalkyl, Halogenalkenyl, Halogenalkinyl, Alkoxy, Alkenyloxy, Alkinyloxy, Halogenalkoxy, Alkoxyalkyl, Alkylamino, Di-(alkyl)amino, Alkylthio, Halogenalkylthio, Alkylsulfinyl, Halogenalkylsulfinyl, Alkylsulfonyl, Halogenalkylsulfonyl oder COR 7 ; R 4 , R 5 , R 6 : Wasserstoff, Halogen, Cyano, Alkyl, Halogenalkyl, Alkoxy, Halogenalkoxy, Alkylthio, Halogenalkylthio, Alkylsulfonyl oder Halogenalkylsulfonyl; R 7 :? ¿Wasserstoff, Hydroxy, Alkyl, Alkoxy, Amino, Alkylamino oder Di(alkyl)amino; sowie deren landwirtschaftlich brauchbaren Salze; Verfahren und Zwischenprodukte zu ihrer Herstellung; sowie die Verwendung dieser Verbindungen oder diese enthaltende Mittel zur Bekämpfung unerwünschter Pflanzen.
Abstract:
Die Erfindung betrifft 4-alkylsubstituierte Thienyloxy-Pyridine der Formel (I), in der die Variablen die folgenden Bedeutungen haben: R 1 , R 3 : Wasserstoff, Halogen, Cyano, Nitro, Alkyl, Halogenalkyl. Alkoxy oder Halogenalkoxy; R 2 : Alkyl oder Cycloalkyl; R 4 , R 5 , R 6 : Wasserstoff, Halogen, Cyano, Alkyl, Halogenalkyl, Alkoxy, Halogenalkoxy, Alkylthio, Halogenalkylthio, Alkylsulfonyl oder Halogenalkylsulfonyl; wobei R 2 nicht Methyl ist, wenn R 1 und R 3 Wasserstoff sind; sowie deren landwirtschaftlich brauchbaren Salze; Verfahren und Zwischenprodukte zu ihrer Herstellung; sowie die Verwendung dieser Verbindungen oder diese enthaltende Mittel zur Bekämpfung unerwünschter Pflanzen.