Enantioselective Mannich reaction of β-keto esters with aromatic and aliphatic imines using a cooperatively assisted bifunctional catalyst

Org Lett. 2014 Oct 3;16(19):5152-5. doi: 10.1021/ol5025025. Epub 2014 Sep 17.

Abstract

An efficient urea-enhanced thiourea catalyst enables the enantioselective Mannich reaction between β-keto esters and N-Boc-protected imines under mild conditions and minimal catalyst loading (1-3 mol %). Aliphatic and aromatic substituents are tolerated on both reaction partners, affording the products in good enantiomeric purity. The corresponding β-amino ketones can readily be accessed via decarboxylation without loss of enantiomeric purity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Decarboxylation
  • Esters
  • Imines / chemistry*
  • Ketones / chemical synthesis*
  • Ketones / chemistry
  • Molecular Structure
  • Stereoisomerism
  • Thiourea / chemistry*
  • Urea / chemistry*

Substances

  • Esters
  • Imines
  • Ketones
  • Urea
  • Thiourea