Conjugate hydrotrifluoromethylation of α,β-unsaturated acyl-oxazolidinones: synthesis of chiral fluorinated amino acids

Org Biomol Chem. 2012 Nov 21;10(43):8583-6. doi: 10.1039/c2ob26810h.

Abstract

A novel conjugate hydrofluoroalkylation of α,β-unsaturated acyl-oxazolidinones is described. Using this method, enantiomerically pure β-trifluoromethylated amino acids were prepared. Trifluorovaline and trifluoroisoleucine were incorporated into peptides and found to show extremely low α-helix propensities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemical synthesis*
  • Amino Acids / chemistry*
  • Methylation
  • Models, Molecular
  • Molecular Structure
  • Oxazolidinones / chemistry*
  • Stereoisomerism

Substances

  • Amino Acids
  • Oxazolidinones