Primary amine-metal Lewis acid bifunctional catalysts based on a simple bidentate ligand: direct asymmetric aldol reaction

Chem Commun (Camb). 2011 Jan 7;47(1):224-6. doi: 10.1039/c0cc00917b. Epub 2010 Jun 21.

Abstract

A novel class of primary amine-metal Lewis acid bifunctional catalysts based on a bidentate ligand was developed. These catalysts were highly efficient in catalyzing the direct asymmetric aldol reactions of ketones offering excellent stereoselectivity. The aldol reactions required a low catalyst loading (2.5 mol%), and were water compatible.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemical synthesis*
  • Alcohols / chemistry
  • Aldehydes / chemistry*
  • Amines / chemistry*
  • Catalysis
  • Copper / chemistry*
  • Ketones / chemistry*
  • Ligands
  • Molecular Structure
  • Stereoisomerism

Substances

  • Alcohols
  • Aldehydes
  • Amines
  • Ketones
  • Ligands
  • Copper