| 摘要 |
Novel benzamidoxime derivatives, processes and intermediates for their preparation and their use as fungicides are described. In the context of the present invention, benzamidoxime derivatives are compounds of the formula I where: A is an aryl or hetaryl radical; Y is a straight-chain or branched C<SUB>1</SUB>-C<SUB>4</SUB>-alkylene group, where one carbon can be replaced by oxygen, nitrogen or sulfur or by a cyclopropyl group; R<SUB>n</SUB><SUP>1 </SUP>are one to five identical or different radicals from the group consisting of: hydrogen, halogen, C<SUB>1</SUB>-C<SUB>6</SUB>-alkyl, C<SUB>1</SUB>-C<SUB>6</SUB>-alkoxy, C<SUB>1</SUB>-C<SUB>4</SUB>-haloalkyl, C<SUB>1</SUB>-C<SUB>4</SUB>-haloalkoxy, C<SUB>1</SUB>-C<SUB>4</SUB>-alkylthio, C<SUB>1</SUB>-C<SUB>4</SUB>-alkoxyalkoxy; R<SUP>2 </SUP>is unsubstituted or substituted phenyl-C<SUB>1</SUB>-C<SUB>6</SUB>-alkyl, thienyl-C<SUB>1</SUB>-C<SUB>4</SUB>-alkyl, or pyrazolyl-C<SUB>1</SUB>-C<SUB>4</SUB>-alkyl, R<SUB>p</SUB><SUP>3 </SUP>are one to five identical or different radicals from the group consisting of: hydrogen, halogen, C<SUB>1</SUB>-C<SUB>6</SUB>-alkyl, C<SUB>1</SUB>-C<SUB>6</SUB>-alkoxy, C<SUB>1</SUB>-C<SUB>4</SUB>-haloalkyl, C<SUB>1</SUB>-C<SUB>4</SUB>-haloalkoxy, C<SUB>1</SUB>-C<SUB>4</SUB>-alkylthio, C<SUB>1</SUB>-C<SUB>4</SUB>-alkoxyalkoxy, C<SUB>1</SUB>-C<SUB>6</SUB>-alkylcarbonyl; n is 0-5; p is, depending on the number of free valencies, 0-4.
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