| abstract |
A fungicide-active compound of the formula is described, wherein Q is a —NY — NH—, —N = N— or, X is an oxygen, sulfur, sulfoxide or sulphonic group; n is 0 or 1; Y is hydrogen, C — C-alkanoyl, C — C-haloalkanoyl, linear or branched C 6 -C-alkoxycarbonyl, C 1-4-alkoxy (C 1 -C 6) alkoxycarbonyl, C 1 -C 6 -alkyl or C 1-6 -haloalkyl; R 5 is C 1 -C 6 -alkoxy, branched C 1 -C 6 alkoxy, C 1 2 -C 5 cycloalkoxy, phenoxy, benzyloxy, C 1 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 3 C 2 3 3 4 C 4 -C 6 -alkoxy, branched C 1 -C 6 alkoxy, C 1 2 -C 5 cycloalkoxy, phenoxy, benzyloxy, 1 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 3 C 6 -C 6-alkoxy, C 1 -C 6-cycloalkoxy, phenoxy, benzyloxy, C 2 -C 2 -alkenyloxy, C 1 2 2 2 2 2 2 2 2 C 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 3 C 2 0 C 1 -C 4 -alkoxy, branched C 2 -C 6 -alkoxy, C 1 2 2 5 C 1 2 5 cycloalkoxy, phenoxy 1 alkoxy) carbonylmethoxy, C — C-thioalkoxy, C — C-alkylamino, C — C-alkyl, branched C – C-alkyl, (C-C-alkoxy) C-C-alkoxy or (C-C-alkoxy) carbonyl ; R5 and R4 are each independently hydrogen, halogen, C 1 -C 6 -alkyl, branched C 1 -C 6 alkyl, C 1 -C 5 haloalkyl, C 2 6 -alkoxy, C 1 6 -haloalkoxy, cyano or (C 1 2 2 -alkoxy) a) carbonyl; R 5 is C 1 -C 2 -alkyl and Z 3 and Z 3 are each independently carbon or nitrogen, provided that when Z is carbon, X is oxygen and R is hydrogen, then R may not be hydrogen; or where R <1> is C-C-alkyl and R <5> and R <1> represent, independently, halogen or C-C-halogenoalkyl, and a method for controlling fungi using the compound. |