| 摘要 |
Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof,;;wherein
G is phenyl, pyridinyl, pyridazinyl or pyrazinyl substituted with Q meta or para to the —C(R2a)R2b— radical, and optionally substituted with up to 3 substituents selected from R3;and A, Z, R1, R2a, R2b, R3 and Q are as defined in the disclosure.;Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling plant disease caused by a fungal plant pathogen comprising applying an effective amount of a compound or a composition of the invention. |
| 主权项 |
1. A compound selected from Formula 1, N-oxides and salts thereof,wherein
A is a radical selected from the group consisting of Z is O or S; R1 is C3-C5 cycloalkyl; or a 4- to 6-membered ring containing ring members selected from carbon atoms, 1O atom and 1S atom; R2a and R2b are each independently H, halogen, C1-C2 alkyl or C1-C2 haloalkyl; or R2a and R2b are taken together as C2-C5 alkanediyl; G is phenyl, pyridinyl, pyridazinyl or pyrazinyl substituted with Q meta or para to the —C(R2a)R2b— radical, and optionally substituted with up to 3 substituents selected from R3; R3 is halogen, nitro, cyano, C1-C5 cyanoalkoxy, C2-C5 alkynyloxy, C2-C5 alkenyl, C1-C5 alkyl, C1-C5 haloalkyl, C1-C5 alkoxy, C1-C5 haloalkoxy, C2-C5 alkoxyalkyl, C3-C5 cycloalkyl, C2-C5 alkoxycarbonyl or C3-C12 trialkylsilyl; R4 is halogen, C1-C3 alkyl or C1-C3 haloalkyl; R5 is H, halogen, C1-C3 alkyl or C1-C3 haloalkyl; R6 is C1-C2 alkyl; R7 is halogen, C1-C3 alkyl or C1-C3 haloalkyl; R8 is H, C1-C2 alkyl or C1-C2 haloalkyl; R9 is halogen, C1-C3 alkyl or C1-C3 haloalkyl; R10 is halogen, C1-C3 alkyl or C1-C3 haloalkyl; R11 is halogen, C1-C3 alkyl or C1-C3 haloalkyl; m is 0, 1 or 2; Q is a 5-membered unsaturated or partially unsaturated heterocyclic ring containing ring members selected from carbon atoms and up to 4 heteroatoms independently selected from up to 1O, up to 1S and up to 4 N atoms, wherein up to 2 carbon atom ring members are independently selected from C(═O), the ring optionally substituted with one substituent on a ring member distal relative to the ring member connecting the heteroaromatic ring to the remainder of Formula 1, said optional substituent selected from R12c on carbon atom ring members and from R12n on nitrogen atom ring members, the heterocyclic ring further optionally substituted with substituents selected from R13c on carbon atom ring members and R13n on nitrogen atom ring members; each R12c is independently halogen, cyano, C1-C3 alkyl, C1-C3 haloalkyl, C1-C3 alkoxy, C1-C3 haloalkoxy or C2-C3 alkoxycarbonyl; or a phenyl ring optionally substituted with up to 5 substituents independently selected from R14; or a heteroaromatic ring optionally substituted with up to 4 substituents independently selected from R15c on carbon atom ring members and from R15n on nitrogen atom ring members; or two R12c bonded to adjacent carbon atoms are taken together with carbon atom ring members to form a 5- or 6-membered carbocyclic or partially aromatic ring; each R12n is independently C1-C3 alkyl, C1-C3 haloalkyl or C1-C3 alkoxy; or a phenyl ring optionally substituted with up to 5 substituents independently selected from R16; or a heteroaromatic ring optionally substituted with up to 4 substituents independently selected from R17c on carbon atom ring members and from R17n on nitrogen atom ring members; each R13c is independently halogen, C1-C3 alkyl, C1-C3 haloalkyl or C1-C3 alkoxy; each R13n is independently C1-C3 alkyl, C1-C3 haloalkyl or C1-C3 alkoxy; each R14, R15c, R16 and R17c is independently halogen, cyano, C1-C2 alkyl, C1-C2 haloalkyl, C1-C2 alkoxy or C1-C2 haloalkoxy; and each R15n and R17n is independently C1-C2 alkyl, C1-C2 haloalkyl or C1-C2 alkoxy. |
