Issue 25, 2013

Efficient catalysts for asymmetric Mannich reactions

Abstract

Efficient chiral catalysts for direct asymmetric three-component Mannich reactions of ketones, aldehydes and an amine (p-anisidine) have been developed. The corresponding β-amino carbonyl compounds (Mannich adducts) were obtained in good chemical yields and excellent enantio- and diastereoselectivities. The reaction conditions have been optimized by invoking ultrasonication and the influence of some structural moieties of the catalysts on the chemical yield and stereoselectivity of the Mannich products has been evaluated.

Graphical abstract: Efficient catalysts for asymmetric Mannich reactions

Article information

Article type
Paper
Submitted
05 Apr 2013
Accepted
01 May 2013
First published
20 May 2013

Org. Biomol. Chem., 2013,11, 4207-4213

Efficient catalysts for asymmetric Mannich reactions

M. Rachwalski, T. Leenders, S. Kaczmarczyk, P. Kiełbasiński, S. Leśniak and F. P. J. T. Rutjes, Org. Biomol. Chem., 2013, 11, 4207 DOI: 10.1039/C3OB40681D

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