Abstract:
Acylierte 4-Aminopyrazole der Formel (I), wobei A für eine der folgenden Gruppen steht: (A 1 ) und (A 2 ), wobei # die Bindung an -C(R 5 R 6 )- bezeichnet und die Variablen die in der Beschreibung genannte Bedeutung haben. Verfahren zur Herstellung der Verbindungen (I), sie enthaltende Mittel und ihre Verwendung zur Bekämpfung von tierischen Schädlingen und Schadpilzen.
Abstract:
The invention relates to the use of substituted imidazoazines of formula (I), in which the variables have the following meanings: R represents alkyl, phenyl, phenylalkyl, naphthyl, anthracenyl, cycloalkyl, 5-membered or 6-membered hetaryl or 5-membered or 6-membered heterocyclyl, containing one to three N atoms and/or one O atom or S atom or one or two O atoms and/or S atoms, or condensed 8-membered to 12-membered hetaryl or condensed 8-membered to 12-membered heterocyclyl, containing one to four N atoms and/or one O atom or S atom or one or two O atoms and/or S atoms, whereby R can be unsubstituted or can be substituted as cited in the description; R and R represent hydrogen, alkyl, alkenyl, alkynyl, alkyl halide, alkenyl halide, alkynyl halide, trialkyl silylalkyl, phenyl, phenylalkyl or R and R , together with the bridging N atom, form a 5-membered or 6-membered heterocyclic or heteroaromatic ring, which can be interrupted by one to three N atoms and/or one O atom or S atom or by one or two O atoms and/or S atoms, and which can be substituted; A and B represent N or CR ; R , R and R represent hydrogen, halogen, cyano, nitro, hydroxy, alkyl, alkyl halide, cycloalkyl, alkoxy, alkoxy halide, alkylthio, amino, alkyl amino, dialkylamino, alkenyl, alkenyloxy, alkynyl or alkynyloxy. The inventive compounds are used for controlling phytopathogenic harmful fungi. The invention further relates to agents containing the inventive compounds, to novel imidazoazines, and to methods for the production thereof.
Abstract:
The invention relates to the use of substituted 5-hydroxypyrazoles of formula (I) in which the substituents have the following meanings: B represents aryl or heteroaryl; A represents C=O, C=S or SO2; R represents alkyl, alkyl halide, alkenyl, alkenyl halide, alkynyl or alkynyl halide, cycloalkyl, C3-C10-cycloalkenyl, cycloalkynyl, or aryl, heterocyclyl or heteroaryl; R represents hydrogen; R represents hydrogen, nitro, cyano, N(R')2, alkyl, alkyl halide, alkoxy, alkoxy halide, alkenyl, alkenyl halide, alkynyl or alkynyl halide, whereby R', independent of one another, represents hydrogen or alkyl; or R and R , together, represent a group =O, =S or =N-O-R , whereby R represents hydrogen, alkyl, alkyl halide, alkenyl, alkenyl halide, alkynyl or alkynyl halide; R represents hydrogen, halogen, nitro, cyano N(R')2, alkyl, alkyl halide, COOR', heteroaryl or heterocyclyl. The invention also relates to the use of said compounds for combating harmful fungi, to agents containing the compounds, to novel 5-hydroxypyrazoles and to methods for the production thereof.
Abstract translation:本发明涉及式(I)的5-羟基吡唑啉的用途,其中取代基具有以下含义:B芳基或杂芳基; A C = O,C = S或SO 2; R 1是烷基,卤代烷基,烯基,卤代烯基,炔基或卤代炔基,环烷基,C 3 -C 10 - 环烯基,环炔基或芳基,杂环基或杂芳基; R 2氢; [R <3>为氢,硝基,氰基,N(R ')2,烷基,卤代烷基,烷氧基,卤代烷氧基,链烯基,卤代烯基,炔基或卤代炔基,其中R' 独立地为氢或烷基; 或R <2>和R <3>一起表示基团= O,= S或= N-O-R <5>,其中R <5>是氢,烷基,卤代烷基,链烯基,卤代烯基,炔基或卤代炔基; R 4是氢,卤素,硝基,氰基,N(R')2,烷基,卤代烷基,COOR',杂芳基或杂环基; 用于控制有害真菌,含有它们的试剂和新的5-羟基吡唑及其制备方法。
Abstract:
The invention concerns pyridyl-phenyl- and benzylethers of formula (I), and their salts and N-oxides, in which the substituents and indices have the following meanings: Q is C(CO2CH3)=CHCH3, C(CO2CH3)=CHOCH3, C(CONH2)=NOCH3, C(CO2CH3)=NOCH3, C(CONHCH3)=NOCH3 or N(OCH3)-CO2CH3; n is 0 or 1; R is hydrogen or an organic group bonded via a carbon atom; R is hydrogen, cyano, halogen or an organic group bonded via a carbon, oxygen, sulphur or nitrogen atom; R is hydrogen, halogen, C1-C4 alkyl or C1-C2 alkyl halide; x is 0, 1 or 2; R is cyano, nitro, halogen or an organic group bonded via a carbon, oxygen, sulphur or nitrogen atom; y is 0, 1, 2 or 3; and R is cyano, halogen, C1-C4 alkyl, C1-C4 alkyl halide or C1-C4 alkoxy. The invention further concerns a process and intermediate products for preparing these substances and their use.
Abstract:
Compounds of the general formula (I) and their salts, in which the variables mean: n is 0, 1, 2, 3 or 4, where the radical R may be different if n is greater than 1; Q is -C(=CHCH3)-COOCH3, -C(=CHOCH3)-COOCH3, -C(=NOCH3)-COOCH3 or -C(=NOCH3)-NH(CH3); Het is a possibly substituted pyrazol ring; R is nitro, cyano, halogen, C1-C4 alkyl, C1-C4 halogen alkyl, C1-C4 alkoxy, C1-C4 halogen alkoxy, C1-C4 alkylthio or possibly substituted phenyl, phenoxy or, if n is greater than 1, a possible substituted 1,3 butadiene-1,4-diyl group bonded to two adjacent carbon atoms of the phenyl radical; R is hydrogen or a possible substituted one or two-nuclear carbo or heterocyclic aromatic ring which is bonded to the radical Het directly or via a (-CR R -) [R , R = H or alkyl or -CR R - = (-C(=O)-) or (-C(=NOR )-); R = alkyl or alkinyl], agents containing them and the use of the compounds (I) and the agents to combat damaging fungi and animal pests.
Abstract:
The invention concerns phenylacetic acid derivatives of formula (I), in which the variables have the following meanings: X = NOCH3, CHOCH3 or CHCH3; Y = O or NZ, Z standing for hydrogen or alkyl; R = H or alkyl; R = cyano, nitro, trifluoromethyl, halogen, alkyl or alkoxy; m = 0, 1 or 2, wherein the group R can be different when m = 2; R = H, cyano, alkyl, alkyl halide, alkoxy or cyclopropyl; R = alkylenedioxy, the alkylene groups being partially or completely halogenated, or one of the groups: -(C=O)-R , -C(=NOR )-Ap-R , -NR -(C=O)-Ap-R , -O-(C=O)-NR R or -N(R )-OR , R , R , independently of each other, being H or optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, heterocyclyl, aryl or heteroaryl; R , R , independently of each other, being H or optionally substituted alkyl, alkenyl, alkinyl, alkylcarbonyl, alkenylcarbonyl, alkinylcarbonyl, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, cycloalkyl, cycloalkylcarbonyl, cycloalkyloxycarbonyl, arylcarbonyl or heteroarylcarbonyl; p = 0 or 1; A = O, S or N, the N-atom carrying H or alkyl; n = 1 or 2, wherein the group R can be different when n = 2; and R = H, alkylsulphonyl or optionally substituted alkyl, alkenyl, alkinyl or cycloalkyl. The invention further concerns salts of these substances, a process and intermediate products for their preparation, and their use as fungicides and pesticides.
Abstract:
Compounds of general formula (I) in which R is cyano, halogen, alkyl or alkoxy; n is 0, 1 or 2, in which the components R may be different if n is 2; Het is a 5-membered heteroaromatic substance containing three nitrogen atoms or two nitrogen atoms and one oxygen or sulphur atom bearing a possibly substituted 6-membered aromatic or heteroaromatic substance; process for their production and their use as pesticides and fungicides.
Abstract:
The invention concerns compounds of formula (I) in which the subscript and the substituents are defined as: n is 0 or 1 to 4; X is 0 or S; Y is a five-membered aromatic heterocycle ring; R is nitro, cyano, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, phenyl or phenoxy; R is hydrogen, alkyl, alkenyl, alkinyl or a saturated or unsaturated ring which may include heteroatoms in addition to carbon atoms as ring members.
Abstract:
The present invention relates to the use of strobilurine type compounds of formula I and the N-oxides and the salts thereof for combating phytopathogenic fungi containing a mutation in the mitochondrial cytochrome b gene conferring resistance to Qo inhibitors, and to methods for combating such fungi. The invention also relates to novel compounds, processes for preparing these compounds, to compositions comprising at least one such compound, to plant health 10 applications, and to seeds coated with at least one such compound.
Abstract:
The present invention relates to substituted 1 -{2-[2-halo-4-(4-halogen-phenoxy)- phenyl]-2-alkoxy-3-methyl-butyl}-1H-[1,2,4]triazole compounds of formula I as defined in the description, and the N-oxides, and salts thereof, processes and intermediates for preparing these compounds and also to compositions comprising at least one such compound.. The invention also relates to the use of such compounds and compositions for combating harmful fungi and seed coated with at least one such compound.