Stereospecific Oxidation of Diacetoxyheterobetulin with Ozone and Dimethyldioxirane

Nat Prod Commun. 2016 Apr;11(4):449-52.

Abstract

Stereospecific oxidation of diacetoxyheterobetulin with ozone and dimethyldioxirane led to 3β,28-diacetoxy-18α,19βH-urs-20α,21α-epoxide with yields of 79% and 87%, respectively. Oxidation with ozone was not selective and gave two minor products containing 2lα-hydroxy-20(30)-ene and 21a-hydroxy-20β,28-epoxy-fragments in ring E. The structures of 3β,28-diacetoxy-18α,19βH-urs-20α,21α-epoxide and 3β-diacetoxy-21α-hydroxy-20β,28-epoxy-18α,19βH-ursane were confirmed by X-ray analysis for the first time.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Epoxy Compounds / chemical synthesis*
  • Epoxy Compounds / chemistry*
  • Oxidation-Reduction
  • Ozone / chemistry
  • Stereoisomerism
  • Triterpenes / chemical synthesis*
  • Triterpenes / chemistry*

Substances

  • 3beta,28-diacetoxy-18alpha,19betaH-urs-20alpha,21alpha-epoxide
  • Epoxy Compounds
  • Triterpenes
  • diacetoxyheterobetulin
  • Ozone
  • dimethyldioxirane