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Efficient catalysts for asymmetric Mannich reactions
Tim Leenders,Sylwia Kaczmarczyk,Piotr Kiełbasiński,Stanisław Leśniak,Floris P. J. T. Rutjes
Organic & Biomolecular Chemistry Pub Date : 05/20/2013 00:00:00 , DOI:10.1039/C3OB40681D
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
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