Microbiocidal bicyclic heterocyclic carboxamide derivatives

A compound of formula (I)

• or a stereoisomer, enantiomer, salt, or N-oxide of the compound of formula (I), wherein:
• R1 is phenyl unsubstituted or substituted with 1, 2 or 3 independently selected substituents R11;
• or
• R1 is a 5- or 6-membered monocyclic heteroaryl ring comprising 1, 2 or 3 heteroatoms each independently selected from N, O and S, wherein said heteroaryl ring is unsubstituted or substituted with 1 or 2 independently selected substituents R11;
• R11 is hydroxyl, halogen, mercapto, amino, cyano, methyl, ethyl, propyl, iso-propyl, vinyl, ethynyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy, propyloxy, iso-propyloxy, tert-butoxy, propynoxy, methylsulfanyl, methylsulfonyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, cyclobutyl, or cyclopropyloxy;
• Lr represents a direct bond, —O—, or —O—C(RL1A)(RL1B)—;
• wherein RL1A and RL1B are independently selected from hydrogen or methyl;
• or RL1A and RL1B together with the carbon atom to which they are attached, form a cyclopropyl;
• or
• L1 represents —NR10—(CR2R3)m—wherein R10 is selected from hydrogen or methyl;
• and m is 0 or 1;
• or
• L1 represents
• wherein # marks the bond to the nitrogen atom and the staggered line marks the bond to the group G;
• R2 and R3 are independently selected from hydrogen or methyl;
• and n is 0 or 1;
• R4 and R5 are independently selected from hydrogen, hydroxy, fluoro, methyl, cyano, or methoxy;
• or
• R4 and R5 together with the carbon atom to which they are attached, form a carbonyl, cyclopropyl, or cyclobutyl group;
• G is selected from G-1, G-2, G-3, or G-4, wherein:
• G-1 is phenyl or phenoxy, wherein said phenyl or phenoxy is unsubstituted or substituted with 1, 2 or 3 independently selected substituents RG1;
• G-2 is a 5- or 6-membered monocyclic heteroaryl or heteroaryl-oxy;
• wherein said heteroaryl comprises 1, 2 or 3 heteroatoms each independently selected from N, O and S;
• and wherein said heteroaryl is unsubstituted or substituted with 1 or 2 independently selected substituents RG2;
• G-3 is a 9- or 10-membered heterobicyclic ring system comprising 1, 2 or 3 heteroatoms each independently selected from N, O and S;
• wherein said heterobicyclic ring system is saturated, partially unsaturated, or aromatic;
• and wherein said heterobicyclic ring system is unsubstituted or substituted with 1 or 2 independently selected substituents RG3;
• G-4 is a 9- or 10-membered carbobicyclic ring system;
• wherein said carbobicyclic ring system is saturated, partially unsaturated, or aromatic;
• and wherein said carbobicyclic ring system is unsubstituted or substituted with 1 or 2 independently selected substituents RG4;
• RG1, RG2, RG3, and RG4 are independently hydroxyl, halogen, mercapto, amino, cyano, methyl, ethyl, propyl, iso-propyl, vinyl, ethynyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy, propyloxy, iso-propyloxy, tert-butoxy, propynoxy, methylsulfanyl, methylsulfonyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, cyclobutyl, or cyclopropyloxy;
• A is selected from A-1 to A-17:
• wherein ## marks the bond to —O—R1;
• % marks the bond to —C(O)—N(H)-L1-G;
• and
• R7, R8, R9 are independently selected from hydrogen, fluoro, chloro, bromo, iodo, methyl, ethyl, propyl, isopropyl, allyl, propargyl, cyclopropylmethyl, cyclopentyl,
• cyclohexyl, —C(═O)OCH3, —C(═O)N(CH3)2, 2-(dimethylamino)-2-oxo-ethyl, 2-(methylamino)-2-oxo-ethyl, difluoromethyl, trifluoromethyl, methylsulfonyl, methylsulfanyl, methoxy, ethoxy, cyano, hydroxyl, mercapto, or amino.