Proline-beta(3)-Amino-Ester Dipeptides as Efficient Catalysts for Enantioselective Direct Aldol Reaction in Aqueous Medium

Abstract

Dipeptides obtained from L-proline and beta(3)-L-amino acids are reported to catalyze enantioselective direct aldol reaction in aqueous medium, leading to significant anti: syn diastereomeric ratios and enantiomeric excesses. The simple introduction of a polar substituent at the C-2 position of the beta(3)-L-amino acid was also found to enhance appreciably both diastereo- and enantioselectivity of the catalyst.