Accessible sugars as asymmetric olefin epoxidation organocatalysts: glucosaminide ketones in the synthesis of terminal epoxides

Org Biomol Chem. 2009 Oct 21;7(20):4285-8. doi: 10.1039/b911675c. Epub 2009 Aug 14.

Abstract

A systematically varied series of conformationally restricted ketones, readily prepared from N-acetyl-D-glucosamine, were tested against representative olefins as asymmetric epoxidation catalysts showing useful selectivities against terminal olefins and, in particular, typically difficult 2,2-disubstituted terminal olefins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Carbohydrates / chemistry*
  • Catalysis
  • Epoxy Compounds / chemical synthesis*
  • Epoxy Compounds / chemistry*
  • Ketones / chemistry
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Alkenes
  • Carbohydrates
  • Epoxy Compounds
  • Ketones