Abstract:
Substituted 6-(2-tolyl)-triazolopyrimidines of formula (I) in which R and R independently denote hydrogen or alkyl, alkenyl, alkynyl, or alkadienyl, haloalkyl, haloalkenyl, cycloalkyl, phenyl, naphthyl, or 5- or 6-membered heterocyclyl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or 5- or 6-membered heteroaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, or where R and R radicals may be unsubstituted or substituted as defined in the description, or R and R together with the interjacent nitrogen atom represent a 5- or 6-membered heterocyclic ring, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom, which may be substituted; R is halogen, cyano, alkyl, alkoxy, haloalkyl, or C(=O)A, wherein A is hydrogen, hydroxy, alkyl, amino, or mono- or dialkyl-amino; n is an integer from 1 to 4; and X is halogen, cyano, alkyl, alkoxy, haloalkoxy or alkenyloxy; processes for their preparation, compositions containing them and to their use for combating phytopathogenic fungi.
Abstract:
The invention relates to 5-phenylpyrimidine of formula (I) wherein the substituents have the following designations: R represents a five to ten-membered saturated, partially unsaturated or aromatic monocyclic or bicyclic heterocycle which contains between one and four heteroatoms from the group 0, N or S, and which can be substituted as defined in the description; R represents hydrogen, halogen, cyano, alkyl, halogenalkyl or alkoxy; R and R represent hydrogen, alkyl, halogenalkyl, cycloalkyl, halogencycloalkyl, alkenyl, halogenalkenyl, cycloalkenyl, alkinyl, halogenalkinyl or cycloalkinyl; together with the nitrogen atom to which they are bonded, R and R can also form a five or six-membered ring which can be split by a heteroatom and can carry at least one substituent; R and R represent hydrogen, halogen, alkyl, halogenalkyl or alkoxy; R and R represent hydrogen, halogen, alkyl or halogenalkyl; and R represents hydrogen, halogen, alkyl, alkoxy, cycloalkoxy, halogenalkoxy or alkoxycarbonyl. The invention also relates to methods and intermediate products for producing said compounds and the use of the same for controlling pathogenic fungi.
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 relates to fungicidal mixtures containing a synergistically effective quantity of at least one compound selected from the following: a) carbamates of formula (I) wherein T means CH or N, n represents 0, 1 or 2 and R means halogen, C1-C4 alkyl or C1-C4 alkyl halide, and the radicals R can be different if n represents 2; a2) the oximethercarboxylic acid ester of formula (II) or a3) the oximethercarboxylic acid amide of formula (III); and b) a compound of formula (IV) wherein the substituents R1 to R3 have the following meaning: R1 is C1-C4 alkyl, C2-C4 alkenyl, C2-C4 alkinyl, C1-C4-alkyl-C3-C7-cycloalkyl and these radicals may carry substituents chosen from the following: halogen, cyano and C1-C4 alkoxy, R2 is C1-C4 alkyl or C1-C4 alkyl halide; R3 is hydrogen, halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkylthio, N--C1-C4-alkylamino, C1-C4 alkyl halide or C1-C4 halogenalkoxy; Y is O, S, CHR4 or NR5, R4 and R5 having the meanings given for R2 and n has the value 0, 1, 2 or 3. The invention also relates to methods for combating harmful fungi using these mixtures.
Abstract:
The invention relates to a fungicidal mixture, containing a synergistically effective amount of a) a phenyl-benzyl ether derivative of formula (I.a) or (I.b) and b) (~)-(2-chlorophenyl)(4-chlorophenyl)(pyrimidin -5- yl) methanol (II).
Abstract:
This invention concerns fungicide mixtures containing in a synergistically effective amount (a) an oxime ether of the formula (I) in which the substituents have the following meaning: X is oxy-gen or amino (NH); Y is CH or N; Z is oxygen, sulphur, amino (NH) or C1-C4-alkylamino (N-C1-C4-alkyl); R' is C1-C6-alkyl, C1-C6-alkyl halide, C3--C6-alkenyl, C2-C6-alkenyl halide, C3--C6-alkinyl, C3-C6-alkinyl halide, C3-C6--cycloalkyl-methyl or benzyl, which can be either partially or completely halogenized and/or can carry one to three of the following radicals: cyano, C1-C4-alkyl, C1-C4-alkyl halide, C1-C4-alkoxy, C1--C4-alkoxy halide, and C1-C4-alkylthio, and/or (b) a carbamate of the formula (II) in which T means CH or N, n is 0, 1, or 2 and R means halogen, C1--C4-alkyl, C1-C4-alkyl halide, where the radicals can be different, if n is 2, and (c) a morpholine or piperidine derivative (III) selected from the group of compounds (IIIa), (IIIb), (IIIc).
Abstract:
The invention concerns a fungicidal mixture which contains in a synergistically effective amount: a) a carbamate of formula (I), in which X means CH and N, n stands for 0, 1 or 2 and R means halogen, C1-C4 alkyl and C1-C4 alkyl halide, wherein the R groups can be different when n stands for 2, one of its salts or adducts; and b) an anilide of formula (II), in which R1 stands for fluorine or chlorine, or one of its salts or adducts.
Abstract:
Je popsán prostředek pro potírání škodlivých hub, který obsahuje v pevném nebo v kapalnémnosiči (A) alespoň jednu účinnou látku obecného vzorce I a (B) alespoň jednu amidovou sloučeninu obecného vzorce II, a kde sloučenina obecného vzorce I a sloučenina obecného vzorce II sepoužijí v hmotnostním poměru od 20 : 1 do 1 :20 k dosažení synergického účinku. Je také popsán způsob potírání škodlivých hub, přikterém se houby, jejich životní prostředí, nebo materiály, rostliny, semena, půda, plochy, nebo prostory, které se mají ochránit před infikováním houbami, ošetřují uvedeným prostředkem.