Amine-promoted, organocatalytic aziridination of enones

Org Lett. 2007 Jan 18;9(2):351-3. doi: 10.1021/ol062852v.

Abstract

A novel method is presented using N-N ylides (prepared by in situ amination of a tertiary amine) for the aziridination of a range of enone systems. The amine may be used sub-stoichiometrically, and promising levels of enantioselectivity are observed with quinine as promoter. [reaction: see text].

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines / chemistry*
  • Aziridines / chemical synthesis*
  • Aziridines / chemistry
  • Catalysis
  • Ketones / chemistry*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Amines
  • Aziridines
  • Ketones