Organocatalytic and highly enantioselective direct alpha-amination of aromatic ketones

Org Lett. 2007 Aug 30;9(18):3671-4. doi: 10.1021/ol701648x. Epub 2007 Aug 11.

Abstract

The first highly enantioselective direct alpha-amination of aryl ketones was reported to be catalyzed by organic primary amines derived from cinchona alkaloids. Excellent enantioselectivities (88-99% ee) have been achieved for a broad spectrum of aryl ketones. The presence of 4 A molecular sieves was of great assistance for the high conversions and enantiocontrol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amination
  • Amines / chemistry*
  • Catalysis
  • Hydrocarbons, Aromatic / chemistry*
  • Ketones / chemistry*
  • Organic Chemicals / chemical synthesis
  • Organic Chemicals / chemistry
  • Stereoisomerism

Substances

  • Amines
  • Hydrocarbons, Aromatic
  • Ketones
  • Organic Chemicals