Abstract

Novel chiral glycinate derivatives (S)-6 and (S)-7 contain- ing the a-phenylethyl group, were prepared and studied as potential precursors of enantiopure a-substituted-a-amino acids. In particu- lar, the alkylation of enolate (S)-7-Li showed substantial (78:22 dr) stereoinduction by the N-(1-phenylethyl)benzamide chiral auxiliary. Addition of DMPU showed no appreciable effect upon the diastere- oselectivity.

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