Azabicyclyl-substituted heterocycles as fungicides

A compound of formula (I):

• wherein
• A1 is N or CR8;
• A2 is O, S, C(═O), S(═O), S(═O)2, NR1 or CR2AR2B,
• wherein
• R1, R2A and R2B are independently from each other hydrogen, C1-C6-alkyl or C3-C8-cycloalkyl,
• wherein C1-C6-alkyl is optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• and
• wherein C3-C8-cycloalkyl is optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, oxo, methylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-halo-alkoxy, C2-C6-alkenyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• or
• R2A and R2B form together with the carbon atom to which they are attached to a C3-C8-cycloalkyl-ring or a 3- to 7-membered heterocyclyl-ring,
• m is 0, 1 or 2,
• R3 and R4 are independently hydrogen, halogen, cyano, hydroxyl, formyl, carboxyl, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkylcarbonyl, C1-C6-alkoxycarbonyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl, C6-C14-aryl, 5- to 14-membered heteroaryl, 3- to 14-membered heterocyclyl or —O—Si(C1-C6-alkyl)3,
• wherein C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkylcarbonyl, C1-C6-alkoxycarbonyl, C2-C6-alkenyl, C2-C6-alkynyl and —O—Si(C1-C6-alkyl)3 are optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• and
• wherein C3-C8-cycloalkyl, C6-C14-aryl, 5- to 14-membered heteroaryl and 3- to 14-membered heterocyclyl are optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, oxo, methylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-halo-alkoxy, C2-C6-alkenyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• or
• R3 and R4 form together with the carbon atom to which they are attached to a carbonyl, a methylidene, a C3-C8-cycloalkyl-ring or a 3- to 7-membered heterocyclyl-ring,
• wherein C3-C8-cycloalkyl-ring and 3- to 7-membered heterocyclyl-ring are optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, oxo, methylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• R5 is hydrogen, hydroxyl, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkylcarbonyloxy, C1-C6-alkyl-sulfanyl, C1-C6-alkylsulfinyl, C1-C6-alkylsulfonyl, C3-C8-cycloalkyl or —O—Si(C1-C6-alkyl)3, wherein C1-C6-alkyl, C1-C6-alkoxy, C1-C6-alkylcarbonyloxy, C1-C6-alkylsulfanyl, C1-C6-alkylsulfinyl, C1-C6-alkylsulfonyl and —O—Si(C1-C6-alkyl)3 are optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxy-carbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• and
• wherein C3-C8-cycloalkyl is optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, oxo, methylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• or
• R3 and R5 or R4 and R5 form together with the carbon atoms to which they are attached to a C3-C8-cycloalkyl-ring,
• T is hydrogen, hydroxyl, C1-C6-alkyl, —C(═O)R9, —C(═O)(OR10), C(═O)N(R11)2, —S(═O)R12, —S(═O)2R13 or —S(═O)2N(R14)2,
• wherein
• R9 and R10 are independently C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl or C2-C6-alkenyl,
• R11, R12, R13 and R14 are independently hydrogen, C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl or C2-C6-alkenyl,
• L is a direct bond, carbonyl, C1-C6-alkylene, C2-C6-alkenylene, C2-C6-alkynylene, —C(═O)—C1-C6-alkylene-, —C1-C6-alkylene-C(═O)—, —NRL1—, —NRL2(C═O)—, —C(═O)NRL3—, —NRL4S(═O)2—, —S(═O)2NRL5—, —C(═NORL6)—, —C(═N—N(RL7)2)—, —C(═NRL8)— or a group of formula
• wherein
• said C1-C6-alkylene, C2-C6-alkenylene, C2-C6-alkynylene, —C(═O)—C1-C6-alkylene- and —C1-C6-alkylene-C(═O)— are optionally substituted with one to three substituents LSA,
• # is the point of attachment to the heterocyclyl-moiety,
• ## is the point of attachment to R6,
• L1 is a direct bond or C1-C6-alkylene,
• L2 is a direct bond or C1-C6-alkylene,
• E is C3-C8-cycloalkyl, C3-C8-cycloalkenyl or 3- to 7-membered heterocyclyl,
• wherein said C3-C8-cycloalkyl, C3-C8-cycloalkenyl and 3- to 7-membered heterocyclyl in turn are optionally substituted with one to three substituents LSC,
• RL1, RL2, RL3 and RL4 are independently hydrogen or C1-C6-alkyl,
• RL5, RL6, RL7 and RL8 are independently hydrogen, C1-C6-alkyl, C1-C6-haloalkyl, C3-C8-cycloalkyl or C2-C6-alkenyl,
• LSA is independently halogen, cyano, hydroxyl, carboxyl, methylidene, halomethylidene, C1-C6-alkoxy, C1-C6-haloalkoxy, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, C1-C6-alkoxycarbonyl, —O—Si(C1-C6-alkyl)3 or 3- to 7-membered heterocyclyl,
• and/or
• two substituents LSA that are bound to the same carbon atom form together with the carbon atom which they are attached to a C3-C8-cycloalkyl-ring or a 3- to 7-membered heterocyclyl-ring,
• LSC is independently halogen, cyano, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 or 3- to 7-membered heterocyclyl,
• and/or
• two LSC substituents form together with the carbon atom(s) to which they are attached to a C3-C8-cycloalkyl-ring,
• R6 is C3-C12-carbocyclyl, C6-C14-aryl, 3- to 14-membered heterocyclyl, 5- to 14-membered hetero-aryl, C3-C12-carbocyclyloxy, C6-C14-aryloxy, 5- to 14-membered heteroaryloxy, 3- to 14-membered heterocyclyloxy, C3-C12-carbocyclylsulfanyl, C6-C14-arylsulfanyl, 5- to 14-membered heteroarylsulfanyl, 3- to 14-membered heterocyclylsulfanyl, C3-C12-carbocyclyl-sulfinyl, C6-C14-arylsulfinyl, 5- to 14-membered heteroarylsulfinyl, 3- to 14-membered hetero-cyclylsulfinyl, C3-C12-carbocyclylsulfonyl, C6-C14-arylsulfonyl, 5- to 14-membered heteroaryl-sulfonyl, 3- to 14-membered heterocyclylsulfonyl, C1-C3-alkoxy, C1-C3-haloalkoxy, C1-C3-alkylsulfanyl, C1-C3-alkylsulfinyl or C1-C3-alkylsulfonyl,
• wherein C1-C3-alkoxy, C1-C3-haloalkoxy, C1-C3-alkylsulfanyl, C1-C3-alkylsulfinyl and C1-C3-alkylsulfonyl are substituted with one substituent selected from the group consisting of C3-C12-carbocyclyl, C6-C14-aryl, 3- to 14-membered heterocyclyl and 5- to 14-membered heteroaryl,
• wherein said C3-C12-carbocyclyl, C6-C14-aryl, 3- to 14-membered heterocyclyl and 5- to 14-membered heteroaryl in turn are optionally substituted with one to four R6S substituents,
• wherein C3-C12-carbocyclyl, C6-C14-aryl, 3- to 14-membered heterocyclyl, 5- to 14-membered heteroaryl, C3-C12-carbocyclyloxy, C6-C14-aryloxy, 5- to 14-membered heteroaryloxy, 3- to 14-membered heterocyclyloxy, C3-C12-carbocyclylsulfanyl, C6-C14-arylsulfanyl, 5- to 14-membered heteroarylsulfanyl, 3- to 14-membered heterocyclylsulfanyl, C3-C12-carbocyclyl-sulfinyl, C6-C14-arylsulfinyl, 5- to 14-membered heteroarylsulfinyl, 3- to 14-membered hetero-cyclylsulfinyl, C3-C12-carbocyclylsulfonyl, C6-C14-arylsulfonyl, 5- to 14-membered heteroaryl-sulfonyl and 3- to 14-membered heterocyclylsulfonyl are optionally substituted with one to four R6S substituents,
• wherein
• R6S is independently selected from the group consisting of halogen, cyano, isocyano, nitro, hydroxyl, mercapto, pentafluorosulfanyl, oxo, methylidene, halomethylidene, formyl, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-halo-alkynyl, C2-C6-alkenyloxy, C2-C6-haloalkenyl-oxy, C2-C6-alkylnyloxy, C2-C6-haloalkylnyloxy, C1-C6-alkylsulfanyl, C1-C6-haloalkyl-sulfanyl, C3-C8-cycloalkylsulfanyl, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C3-C8-cycloalkyl-sulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, C3-C8-cyclo-alkylsulfonyl, C3-C8-cycloalkyl, C3-C8-cycloalkyloxy, C3-C8-cycloalkenyl, C6-C14-aryl, 5- or 6-membered heteroaryl, 3- to 7-membered heterocyclyl, —N(R15)2, —O(C═O)R16, —C(═O)R16, —C(═O)(OR17), —C(═O)N(R18)2, —S(═O)2N(R19)2, —O—Si(C1-C6-alkyl)3 and —Si(C1-C6-alkyl)3,
• wherein C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C2-C6-alkenyl-oxy, C2-C6-haloalkenyloxy, C2-C6-alkylnyloxy, C2-C6-haloalkylnyloxy, C1-C6-alkylsulfanyl, C1-C6-haloalkylsulfanyl, C1-C6-alkylsulfinyl, C1-C6-haloalkyl-sulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, —O—Si(C1-C6-alkyl)3 and —Si(C1-C6-alkyl)3 are furthermore optionally substituted with one to three substituents independently selected from the group consisting of cyano, hydroxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, —O—Si(C1-C6-alkyl)3, —Si(C1-C6-alkyl)3, C3-C8-cycloalkyl, C3-C8-halocycloalkyl and 3- to 7-membered heterocyclyl,
• or
• two substituents C1-C6-alkyl attached to the same carbon atom form together with the carbon atom to which they are attached to a C3-C8-cycloalkyl-ring,
• and
• wherein C3-C8-cycloalkylsulfanyl, C3-C8-cycloalkylsulfinyl, C3-C8-cycloalkyl-sulfonyl, C3-C8-cycloalkyl, C3-C8-cycloalkyloxy, C3-C8-cycloalkenyl, C6-C14-aryl, 5- or 6-membered heteroaryl and 3- to 7-membered heterocyclyl are furthermore optionally substituted with one to four substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C1-C6-haloalkoxy-carbonyl, C2-C6-alkenyl, C3-C8-cycloalkyl and C3-C8-halocycloalkyl,
• and wherein
• R15 is independently hydrogen, C1-C6-alkyl or C3-C8-cycloalkyl,
• wherein said C1-C6-alkyl in turn is optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, hydroxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, —O—Si(C1-C6-alkyl)3, —Si(C1-C6-alkyl)3, C3-C8-cycloalkyl, C3-C8-halocycloalkyl and 3- to 7-membered heterocyclyl,
• and
• wherein said C3-C8-cycloalkyl in turn is optionally substituted with one to four substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxy-carbonyl, C1-C6-haloalkoxycarbonyl, C2-C6-alkenyl, C3-C8-cycloalkyl and C3-C8-halocycloalkyl,
• R16, R17, R18 and R19 are independently hydrogen, C1-C6-alkyl or C1-C6-haloalkyl,
• wherein said C1-C6-alkyl and C1-C6-haloalkyl in turn are optionally substituted with one to three substituents independently selected from the group consisting of cyano, hydroxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, —O—Si(C1-C6-alkyl)3, —Si(C1-C6-alkyl)3, C3-C8-cycloalkyl, C3-C8-halocycloalkyl and 3- to 7-membered heterocyclyl,
• the ring Y forms together with the pyridine- or pyridazine-ring respectively a bicyclic hetero-cyclyl or a bicyclic heteroaryl,
• p is 0, 1, 2, 3 or 4,
• R7 is hydrogen, halogen, cyano, isocyano, hydroxyl, mercapto, nitro, amino, formyl, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-hydroxyalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylcarbonyl, C1-C6-haloalkylcarbonyl, C1-C6-alkoxycarbonyl, C1-C6-haloalkoxycarbonyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C2-C6-alkenyloxy, C2-C6-haloalkenyl-oxy, C2-C6-alkynyloxy, C2-C6-haloalkynyloxy, C1-C6-alkylsulfanyl, C1-C6-haloalkylsulfanyl, C3-C8-cycloalkylsulfanyl, C2-C6-alkenylsulfanyl, C2-C6-alkynylsulfanyl, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C3-C8-cycloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkyl-sulfonyl, C3-C8-cycloalkylsulfonyl, C3-C8-cycloalkyl, C3-C6-cycloalkenyl, 3- to 7-membered heterocyclyl, C3-C8-cycloalkyloxy, —O—Si(C1-C6-alkyl)3, —Si(C1-C6-alkyl)3, —N(R20)2, —C(═NR21)R22, —NR23C(═O)R24, —C(═O)(OR25), —C(═O)N(R26)2, —S(═O)2N(R27)2 or —S(═O)(═NR28)R29,
• wherein C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-hydroxyalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylcarbonyl, C1-C6-haloalkylcarbonyl, C1-C6-alkoxycarbonyl, C1-C6-haloalkoxy-carbonyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C2-C6-alkenyl-oxy, C2-C6-haloalkenyloxy, C2-C6-alkynyloxy, C2-C6-haloalkynyloxy, C1-C6-alkylsulfanyl, C1-C6-haloalkylsulfanyl, C2-C6-alkenylsulfanyl, C2-C6-alkynylsulfanyl, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, —O—Si(C1-C6-alkyl)3 and —Si(C1-C6-alkyl)3 are optionally substituted with one to three R7Sa substituents,
• wherein C3-C8-cycloalkylsulfanyl, C3-C8-cycloalkylsulfinyl, C3-C8-cycloalkylsulfonyl, C3-C8-cycloalkyl, C3-C6-cycloalkenyl, 3- to 7-membered heterocyclyl, C3-C8-cycloalkyloxy are optionally substituted with one to three R7Sc substituents,
• and wherein
• R20 is independently hydrogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C3-C8-cycloalkyl, C3-C8-halo-cycloalkyl or 3- to 7-membered heterocyclyl,
• wherein C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C2-C6-alkenyl, C2-C6-halo-alkenyl, C2-C6-alkynyl and C2-C6-haloalkynyl in turn are optionally substituted with one to three substituents R7Sa,
• and
• wherein C3-C8-cycloalkyl, C3-C8-halocycloalkyl and 3- to 7-membered heterocyclyl in turn are optionally substituted with one to three substituents R7Sc,
• R21 and R22 are independently hydroxyl, amino, cyano, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, mono-(C1-C6-alkyl)amino or di-(C1-C6-alkyl)amino,
• wherein C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, mono-(C1-C6-alkyl)-amino and di-(C1-C6-alkyl)amino in turn are optionally substituted with one to three R7Sa substituents,
• R23, R24, R25, R26, R27, R28 and R29 are independently hydrogen, C1-C6-alkyl, C1-C6-halo-alkyl and C3-C8-cycloalkyl,
• wherein C1-C6-alkyl and C1-C6-haloalkyl in turn are optionally substituted with one to three R7Sa substituents,
• and
• wherein C3-C8-cycloalkyl in turn is optionally substituted with one to three R7Sc substituents,
• wherein
• R7Sa is independently cyano, hydroxyl, carboxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, C1-C6-alkoxycarbonyl, —O—Si(C1-C6-alkyl)3, —Si(C1-C6-alkyl)3 or 3- to 7-membered heterocyclyl,
• R7Sc is independently halogen, cyano, nitro, hydroxyl, formyl, oxo, methylidene, halomethylidene, C1-C6-alkyl, C1-C6-haloalkyl C1-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —O—Si(C1-C6-alkyl)3 or 3- to 7-membered heterocyclyl,
• or
• two R75c substituents that are bound to the same carbon atom form together with the carbon atom to which they are attached to a C3-C8-cycloalkyl-ring,
• or
• two R7 substituents form together with the carbon atoms to which they are attached to a C3-C8-cycloalkyl-ring,
• R8 is hydrogen or halogen,
• Q is C6-C14-aryl, C3-C12-carbocyclyl, 3- to 14-membered heterocyclyl or 5- to 14-membered heteroaryl,
• wherein C6-C14-aryl, C3-C12-carbocyclyl, 3- to 14-membered heterocyclyl or 5- to 14-membered heteroaryl are optionally substituted with one to five substituents QS,
• wherein
• QS is independently selected from the group consisting of halogen, cyano, isocyano, nitro, hydroxyl, mercapto, formyl, carboxyl, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkylcarbonyl, C1-C6-haloalkylcarbonyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C1-C6-haloalkoxycarbonyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C2-C6-alkenyloxy, C2-C6-haloalkenyloxy, C1-C6-alkylsulfanyl, C1-C6-haloalkylsulfanyl, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, C3-C8-cycloalkyl, C3-C8-cycloalkyloxy, C3-C6-cycloalkenyl, 3- to 7-membered heterocyclyl, C6-C14-aryl, 5- to 14-membered heteroaryl, —O—Si(C1-C6-alkyl)3, —Si(C1-C6-alkyl)3, —O—C(═O)R30, —NR31C(═O)R32, —C(═O)N(R33)2, C(═S)R34, —C(═S) N(R35)2, —C(═NR36)R37, —C(═NOR38)R39 and —N(R40)2,
• wherein
• said C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkylcarbonyl, C1-C6-haloalkyl-carbonyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkoxycarbonyl, C1-C6-haloalkoxycarbonyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, C2-C6-alkenyloxy, C2-C6-haloalkenyloxy, C1-C6-alkylsulfanyl, C1-C6-haloalkylsulfanyl, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, —O—Si(C1-C6-alkyl)3 and —Si(C1-C6-alkyl)3 in turn are optionally substituted with one to three substituents independently selected from the group consisting of cyano, amino, nitro, hydroxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C1-C6-haloalkoxycarbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• and said C3-C8-cycloalkyl, C3-C8-cycloalkoxy, C3-C6-cycloalkenyl, 3- to 7-membered heterocyclyl and 5- to 14-membered heteroaryl in turn are optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C1-C6-halo-alkoxycarbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, C2-C6-alkenyl and 3- to 7-membered heterocyclyl,
• wherein said C3-C8-cycloalkyl, C3-C8-halocycloalkyl and 3- to 7-membered heterocyclyl furthermore are optionally substituted with two substituents forming together with the carbon atom(s) to which they are attached to a C3-C8-cycloalkyl,
• and wherein
• R30, R31, R32, R33, R34, R35, R36, R37, R38 and R39 are independently hydrogen, C1-C6-alkyl, C1-C6-haloalkyl or C1-C6-alkoxy,
• wherein
• said C1-C6-alkyl, C1-C6-haloalkyl and C1-C6-alkoxy in turn are optionally substituted with one to three substituents independently selected from the group consisting of cyano, amino, nitro, hydroxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C1-C6-halo-alkoxycarbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• and wherein
• R40 is hydrogen, hydroxyl, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C2-C6-alkenyl, C2-C6-haloalkenyl or C3-C8-cycloalkyl,
• wherein said C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C2-C6-alkenyl and C2-C6-haloalkenyl in turn are optionally substituted with one to three substituents independently selected from the group consisting of cyano, amino, nitro, hydroxyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C1-C6-haloalkoxycarbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, —Si(C1-C6-alkyl)3 and 3- to 7-membered heterocyclyl,
• and wherein said C3-C8-cycloalkyl in turn is optionally substituted with one to three substituents independently selected from the group consisting of halogen, cyano, amino, nitro, hydroxyl, formyl, carboxyl, oxo, methylidene, halomethylidene, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkoxycarbonyl, C1-C6-halo-alkoxycarbonyl, C3-C8-cycloalkyl, C3-C8-halocycloalkyl, C2-C6-alkenyl and 3- to 7-membered heterocyclyl,
• wherein said C3-C8-cycloalkyl, C3-C8-halocycloalkyl and 3- to 7-membered heterocyclyl furthermore are optionally substituted with two substituents forming together with the carbon atom(s) to which they are attached to a C3-C8-cycloalkyl,
• or
• two QS substituents that are bound to the same carbon atom form together with the carbon atom to which they are attached to a C3-C8-cycloalkyl-ring,
• as well as N-oxides, salts, hydrates and hydrates of the salts and N-oxides thereof.