Enantioselective reactions are those that yield a single chiral product with a defined stereochemical configuration. In this case, the goal is to create a chiral all-carbon quaternary center with a specific enantiomer (either R or S).
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(S)-4,5,5-trimethyl-4-(4-methylphenyl)-2-cyclopentenone
(1'S,3S)-diethyl-1-benzyl-1'-(4-nitrophenyl)-2-oxo-1',2'-dihydrospiro[indoline-3,4'-pyrido[3,4-b]indole]-3',3'(9'H)-dicarboxylate
