Asymmetric Bio-epoxidation of Unactivated Alkenes

Chembiochem. 2023 Apr 3;24(7):e202200719. doi: 10.1002/cbic.202200719. Epub 2023 Mar 10.

Abstract

Optically active epoxides play important roles in pharmaceutical, agricultural and fine chemical syntheses. There are many chiral medications with pharmacodynamic activity in nature that can be synthesized by chiral epoxides. In recent years, researchers have developed a variety of biocatalysts for the asymmetric epoxidation of alkenes, which use oxygen or hydrogen peroxide as eco-friendly and low-cost oxidants, to provide better chemo-, regio- and stereoselectivity under moderate reaction conditions. In this paper, the advances, opportunities and challenges of the asymmetric epoxidation of unactive alkenes by biocatalyst are reviewed.

Keywords: asymmetric epoxidation; biocatalysis; chiral epoxides; enzymes; unactivated alkenes.

Publication types

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

MeSH terms

  • Alkenes*
  • Catalysis
  • Epoxy Compounds
  • Hydrogen Peroxide
  • Oxidants*
  • Stereoisomerism

Substances

  • Alkenes
  • Oxidants
  • Hydrogen Peroxide
  • Epoxy Compounds