Issue 6, 2010

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

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.

Graphical abstract: Direct asymmetric aldol reactions between aldehydes and ketones catalyzed by l-tryptophan in the presence of water

Supplementary files

Article information

Article type
Paper
Submitted
14 Oct 2009
Accepted
09 Dec 2009
First published
22 Jan 2010

Org. Biomol. Chem., 2010,8, 1368-1377

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

Z. Jiang, H. Yang, X. Han, J. Luo, M. W. Wong and Y. Lu, Org. Biomol. Chem., 2010, 8, 1368 DOI: 10.1039/B921460G

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