摘要

Diastereomeric reduction of nonactivated, hindered beta-keto and chiral beta-iminoesters are described. The influence of a alpha-stereocontrolled center on the efficiency and stereoselectivity of the reduction was studied. Reaction conditions were optimized to synthesize beta-hydroxy- and beta-aminoesters in good yields. In the case of chiral beta-iminoesters, influence of matched/mismatched diastereomeric pairs has been assessed. Chirality 23:265-271, 2011.

  • 出版日期2011-3