Synthesis of Chiral beta 3-aminoxy peptides

J Org Chem. 2004 Oct 29;69(22):7577-81. doi: 10.1021/jo049174f.

Abstract

A series of chiral beta(3)-aminoxy acids or amides with various side chains have been synthesized via two different approaches. One is the Arndt-Eistert homologation approach, using chiral alpha-aminoxy acids as starting materials. The other approach, utilizing the enantioselective reduction of beta-keto esters catalyzed by baker's yeast or chiral Ru(II) complexes, produces chiral beta(3)-aminoxy acids with nonproteinaceous side chains. The oligomers of beta(3)-aminoxy acids can be readily prepared using EDCI/HOAt as the coupling reagent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemical synthesis*
  • Amino Acids / chemical synthesis*
  • Catalysis
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Peptides / chemical synthesis*
  • Stereoisomerism

Substances

  • Amides
  • Amino Acids
  • Peptides