This reaction involves the introduction of an alkyl group onto the lithium enolate of a cyclic ketone. Enantioselective means that the reaction is designed to favor the formation of one enantiomer (chiral isomer) of the product over the other.
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benzyl dibut-3-enylcarbamate
N-[2-bromo-3-hydroxy-1-(SS)(4-methylphenylsulfinylmethyl)-3-phenyl-(1S,2R,3S)-propyl]-4-methyl-1-benzenesulfonamide
2-phenylpropan-2-yl-2-((diphenylmethylene)amino)acetate
