Synthesis of optically active alpha-methylene beta-lactams through lipase-catalyzed kinetic resolution

J Org Chem. 2000 Aug 11;65(16):4919-22. doi: 10.1021/jo0003089.

Abstract

A convenient method for the preparation of the hitherto unknown chiral alpha-methylene beta-lactam derivatives 5a,b is reported. The optically active alpha-methylene beta-lactams 5a-c, and their corresponding amino acids 6a-c have been readily made available through lipase-catalyzed kinetic resolution in high enantiomeric purity (up to 99% ee). The N-substituted beta-lactam derivatives 4a, b and 10 are not accepted by the lipases and were prepared in optically active form by chemical transformation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Circular Dichroism
  • Kinetics
  • Lipase / metabolism*
  • Methylation
  • Models, Chemical
  • Spectrophotometry, Ultraviolet
  • beta-Lactams / chemical synthesis*

Substances

  • beta-Lactams
  • Lipase