The term "allylic alkylation" refers to the addition of an alkyl group to the allylic position of a substrate. In this case, the allylic alkylation is asymmetric, meaning that the reaction yields a chiral product with a specific stereochemistry.
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tert-butyl 3-(1-(4-fluorophenyl)-2-(methoxycarbonyl)allyl)-2-oxo-3-phenylindoline-1-carboxylate
(2R,3R)-ethyl 2-(diethoxyphosphoryl)-2-fluoro-3-phenylpent-4-enoate
methyl [2-cyano-2-m-tolyl]acetate
Benzene, 1-methyl-4-(1-propynyl)- (9CI)
2H-Pyrrol-2-one, 1-acetyl-1,5-dihydro-5-(2-propenyl)-, (R)- (9CI)
(11AR)-(+)-10,11,12,13-TETRAHYDRODIINDENO[7,1-DE:1',7'-FG][1,3,2]DIOXAPHOSPHOCIN-5-PHENOXY
6-Octenoic acid, 8-[(methoxycarbonyl)oxy]-2-[(4-methylphenyl)sulfonyl]-, methyl ester, (E)-
2H-Pyrrole,2-ethenyl-3,4-dihydro-5-methyl-,1-oxide(9CI)
2-allyl-4-(tetrahydro-2H-pyran-2-yloxy)cyclohexanone
