Designing new chiral ketone catalysts. Asymmetric epoxidation of cis-olefins and terminal olefins

J Org Chem. 2002 Apr 19;67(8):2435-46. doi: 10.1021/jo010838k.

Abstract

This paper describes a new class of chiral oxazolidinone ketone catalyst for asymmetric epoxidation. High ee values have been obtained for a number of cyclic and acyclic cis-olefins. The epoxidation was stereospecific with no isomerization observed in the epoxidation of acyclic systems. Encouragingly high ee values have also been obtained for a number of terminal olefins. Mechanistic studies show that electronic interactions play an important role in stereodifferentiation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Chemistry, Organic / methods
  • Chromatography, High Pressure Liquid
  • Crystallography, X-Ray
  • Epoxy Compounds / chemical synthesis*
  • Epoxy Compounds / chemistry*
  • Ketones / chemistry*
  • Magnetic Resonance Spectroscopy
  • Molecular Conformation
  • Molecular Structure
  • Oxidation-Reduction
  • Stereoisomerism

Substances

  • Alkenes
  • Epoxy Compounds
  • Ketones