FIELD: biochemistry. SUBSTANCE: described are N-sulfonyl and N-sulfinylamino acid amides of formula I: R1 wherein n is 0 or 1; C1-C12 is C1-C4 alkyl optionally substituted with alkoxy group, C3-C8 alkylsulfonyl, C1-C6 cycloalkyl or C3-C8- alkoxycarbonyl; C2-C12 cycloalkyl, C1-C12 alkenyl, NR13R14 halogenalkyl or R13 and R14 wherein C1-C6 are independently hydrogen or R2 and R3 alkyl or together are tatra- or pentamethylene; C1-C8 are independently hydrogen; C1-C8 alkyl C1-C4 alkyl which is substituted by hydroxyl, C1-C4 alkoxy group, mercapto group or C3-C8 alkylthio group; C3-C8 cycloalkyl or C1-C4 cycloalkyl-R2 and R3 alkyl, or wherein both groups R4 together with carbon atom to which they attached form 3-8 membered carboxylic ring; C1-C6 is hydrogen or R5 alkyl; C1-C6 is hydrogen; R6 alkyl or phenyl; R7 and R8 is group G wherein C1-C6 are independently hydrogen, R9, R10 and R11 alkyl is 0 or 1; and C1-C6 are independently hydrogen, C1-C6 alkyl, C1-C6 halogenalkyl, C3-C6 alkoxy group, C3-C6 alkenyloxy group, alkynyloxy group, halogen or nitro group. Compounds of formula I have biocidal spectrum of activity for controlling phytopethogenic microorganisms, more particularly fungi. EFFECT: improved properties of the title compounds. 27 cl, 314 ex, 6 tbl
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Authors
Dates
1999-10-27—Published
1995-04-22—Filed