A Grignard reagent (RMgX), where R represents an alkyl or aryl group and X is a halide (usually bromide or chloride), serves as the nucleophilic agent for the conjugate addition. Grignard reagents are strong nucleophiles and can add to electron-deficient alkenes.
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3-methyl-2-phenyl-1-tosyl-but-3-enyl N,N-diisopropylcarbamate
C5H5FeC5H4CH(C6H5)CH2COCH3
1H-Indene-2-thiol, 2,3-dihydro-1,1,3,3-tetramethyl-2-(phenylmethyl)-
1-Amino-2-methylpropan-2-ol
2H-Purin-2-one, 6-ethoxy-1,3,6,7-tetrahydro-1,3,7-tris(phenylmethyl)-
1H-Indole, 1-acetyl-4,6-bis(trimethylsilyl)-
(-)-(4aR,7R)-4,4a,5,6,7,8-hexahydro-7-isopropenyl-4a-methylnaphthalene-2(3H)-one
4,4-Dimethyl-5-oxo-2-phenethyl-tetrahydro-furan-3-carboxylic acid ethyl ester
1H-Pyrazole, 1-(phenylmethoxy)-
2-butyl-1-phenyl-1H-pyrrole
rac-1-phenyl-1-propyl-propionate
THIENO[3,2-B]THIOPHENE-2-CARBOXYLIC ACID
3-benzyl-2-methylene-3-phenyloxetane
(R)-6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylicacid
4-bromo-1,1,2,2-tetrafluorobutane(SALTDATA: FREE)
