Abstract:
The present invention relates to novel triazole compounds of the formulae (I) and (Il) as defined below, to agricultural and pharmaceutical compositions containing them and to their use as fungicides antiviral and anticancer agents.
Abstract:
The invention relates to compounds of formula (I), wherein the variables have the meanings indicated in the claims or the description, and to their agriculturally acceptable salts.
Abstract:
The present invention relates to compounds of formula (I) wherein the variables have the meanings defined in the claims and the specification.
Abstract:
The present invention relates to pyridin-4-ylmethyl sulfonamides of formula I wherein Het, R a , R c , R f , m, n, p, R, A and Y are as defined in the claims, to the N-oxides, and salts thereof and their use for combating harmful fungi, and also to compositions and seed comprising at least one such compound. The invention also relates to a process and intermediates for preparing these compounds.
Abstract:
The present invention relates to the use of substituted sulfonic acid amide compounds of formula I wherein Ra, n, Het, A, Y and D are as defined in the claims and the N-oxides and the salts thereof for combating phytopathogenic harmful fungi, and to compositions and seeds comprising at least one such compound. The invention also relates to novel substituted sulfonic acid amide compounds and processes for preparing these compounds.
Abstract:
The invention relates to the azolylmethyloxiranes of formula (I), wherein variables A, B and D have the meanings as defined in the description and the claims.
Abstract:
The invention relates to thiazole carboxylic acid anilides of formula (I), in which the variables are defined as follows: X represents halogen; Y represents cyano, nitro, C1-C4-alkyl, C1-C4 haloalkyl, methoxy or methylthio; p represents 0.1; R1 represents hydrogen, halogen, C1-C4 alkyl or C1-C4 haloalkyl; R2 represents hydrogen, methyl or halogen; R3 represents hydrogen, methyl or ethyl; W represents O or S. The invention also relates to a method for producing said compounds, to agents containing the latter, to seed and to a method for controlling pathogenic fungi.
Abstract:
The invention relates to 5,6-dialkyl-7-amino-triazolopyrimidines of formula (I), in which the substituents are defined as follows: R1 represents alkyl or alkoxyalkyl, whereby the aliphatic groups can be substituted according to the description; R2 represents CHR3CH3, cyclopropyl, CH=CH2 or CH2CH=CH2 and R3 represents hydrogen, CH3 or CH2CH3. The invention also relates to a method for producing said compounds, to agents containing the latter and to their use for controlling plant-pathogenic fungi.
Abstract:
Die vorliegende Erfindung betrifft 2-(Pyridin -2-yl)-pyrimidine Verbindungen der allgemeinen Formel I und ihre Verwendung zur Bekämpfung von Schadpilzen sowie Pflanzenschutzmittel, die derartige Verbindungen als wirksamen Bestandteil enthalten.
Hierin steht k für 0, 1, 2 oder 3, m für 0, 1, 2, 3, 4 oder 5, n für 1, 2, 3, 4 oder 5; R 1 bedeuten unabhängig voneinander Halogen, OH, CN, NO 2 C 1 -C 4 -Alkyl, C 1 -C 4 -Halogenalkyl, C 1 -C 4 -Alkoxy, C 1 -C 4 -Halogenalkoxy, C 2 -C 4 -Alkenyl, C 2 -C 4 -Alkinyl, C 3 -C 8 -Cycloalkyl, C 1 -C 4 -Alkoxy-C 1 -C 4 -alkyl, Amino, Phenoxy, das gegebenenfalls durch Halogen oder C 1 -C 4 -Alkyl substituiert ist, NHR, NR 2 , C(R a )=N-OR b , S(=O) p A 1 oder C(=O)A 2 , oder zwei an benachbarte C-Atome gebundene Reste R 1 können auch gemeinsam für eine Gruppe -O-Alk-O- stehen, worin Alk für lineares oder verzweigtes C 1 -C 4 -Alkylen steht, worin 1, 2, 3 oder 4 Wasserstoffatome auch durch Halogen ersetzt sein können; R 2 C 1 -C 4 -Halogenalkyl, C 1 -C 4 -Alkoxy, C 1 -C 4 -Halogenalkoxy, Hydroxy, Halogen, CN oder NO 2 bedeutet; wobei R 2 auch Wasserstoff oder C 1 -C 4 -Alkyl bedeuten kann, wenn wenigstens eine der drei folgenden Bedingungen erfüllt ist: - n steht für 3, 4 oder 5, - k steht für 1, 2 oder 3, - für m ≠ 0 steht wenigstens einer der Reste R 1 für einen von Halogen, C 1 -C 4 -Alkyl, C 1 -C 4 -Alkoxy und C 1 -C 4 -Halogenalkyl verschieden Rest; und R 3 für C 1 -C 4 -Alkyl.
Abstract:
The invention relates to 2-(pyridin-2-yl)-pyrimidine compounds of general formula (I) and their use for controlling pathogenic fungi and as plant protection products that, as an active constituent, contain compounds of this type, whereby: k represents 0, 1, 2, 3; m represents 0, 1, 2, 3, 4 or 5; n represents 1, 2, 3, 4 or 5; R1, independent of one another, represents halogen, OH, CN, NO2, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy, C1-C4 alkoxy halide, C2-C4 alkenyl, C2-C4 alkynyl, C3-C8 cycloalkyl, C1-C4 alkoxy-C1-C4 alkyl, amino, phenoxy, which is optionally substituted by halogen or C1-C4 alkyl, NHR, NR2, C(Ra)=N-ORb, S(=O)pA1 or C(=O)A2, or two radicals R1 bound to adjacent carbon atoms can, together, also represent a group -O-Alk-O-, wherein Alk represents a linear or branched C1-C4 alkylene, and 1, 2, 3 or 4 hydrogen atoms can also be replaced by halogen; R2 represents C1-C4 alkyl halide, C1-C4 alkoxy, C1-C4 alkoxy halide, hydroxy, halogen, CN or NO2; whereby R2 can also represent hydrogen or C1-C4 alkyl when at least one of the three following conditions is fulfilled: n represents 3, 4 or 5; k represents 1, 2 or 3; if m is not equal to 0, at least one of the radicals R1 represents a radical that differs from halogen, C1-C4 alkyl, C1-C4 alkoxy and C1-C4 alkyl halide, and; R3 represents C1-C4 alkyl.