Enantioconvergent hydrolysis of styrene epoxides by newly discovered epoxide hydrolases in mung bean

Org Lett. 2006 Apr 13;8(8):1737-40. doi: 10.1021/ol060407u.

Abstract

[reaction: see text] Two novel epoxide hydrolases were discovered in mung bean (Phaseolus radiatus L.) for the first time, either of which can catalyze enantioconvergent hydrolysis of styrene epoxides. Their regioselectivity coefficients are more than 90% for the p-nitrostyrene oxide. Furthermore, the crude mung bean powder was also shown to be a cheap and practical biocatalyst, allowing a one-step asymmetric synthesis of chiral (R)-diols from racemic epoxides, in up to >99% ee and 68.7% overall yield (after recrystallization).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Epoxide Hydrolases / chemistry
  • Epoxide Hydrolases / isolation & purification*
  • Epoxy Compounds / chemistry*
  • Fabaceae / chemistry*
  • Hydrolysis
  • Molecular Structure
  • Plants, Medicinal / chemistry*
  • Stereoisomerism
  • Styrene / chemistry*

Substances

  • Epoxy Compounds
  • Styrene
  • Epoxide Hydrolases