Direct asymmetric aldol reactions between aldehydes and ketones catalyzed by L-tryptophan in the presence of water

Org Biomol Chem. 2010 Mar 21;8(6):1368-77. doi: 10.1039/b921460g. Epub 2010 Jan 22.

Abstract

Primary amino acids and their derivatives were investigated as catalysts for the direct asymmetric aldol reactions between ketones and aldehydes in the presence of water, and L-tryptophan was shown to be the best catalyst. Solvent effects, substrate scope and the influence of water on the reactions were investigated. Quantum chemical calculations were performed to understand the origin of the observed stereoselectivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemistry*
  • Catalysis
  • Ketones / chemistry*
  • Models, Molecular
  • Molecular Conformation
  • Quantum Theory
  • Solvents / chemistry
  • Stereoisomerism
  • Substrate Specificity
  • Tryptophan / chemistry*
  • Water / chemistry*

Substances

  • Aldehydes
  • Ketones
  • Solvents
  • Water
  • Tryptophan