Formation of enantiopure 5-substituted oxazolidinones through enzyme-catalysed kinetic resolution of epoxides

Org Lett. 2008 Jun 19;10(12):2417-20. doi: 10.1021/ol800698t. Epub 2008 May 21.

Abstract

Halohydrin dehalogenase from Agrobacterium radiobacter catalyzed the enantioselective ring opening of terminal epoxides with cyanate as a nucleophile, yielding 5-substituted oxazolidinones in high yields and with high enantiopurity (69-98% ee). This is the first example of the biocatalytic conversion of a range of epoxides to the corresponding oxazolidinones.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Epoxy Compounds / chemistry*
  • Hydrolases / metabolism*
  • Kinetics
  • Molecular Structure
  • Oxazolidinones / chemical synthesis*
  • Oxazolidinones / chemistry
  • Rhizobium / enzymology*
  • Stereoisomerism

Substances

  • Epoxy Compounds
  • Oxazolidinones
  • Hydrolases
  • halohydrin dehalogenase