Bile acids in asymmetric synthesis and chiral discrimination
Copyright policy )Bile acids in asymmetric synthesis and chiral discrimination
AbstractAn overview on the use of bile acid‐based compounds able to catalyze transformations, control the stereochemical course of a given reaction, recognize and bind other molecules, is presented. The recent developments in inclusion discrimination of chiral and achiral guests and enantioselective recognition achieved by bile acid are described with suitable examples. Chirality 2010. © 2009 Wiley‐Liss, Inc.
- University of Calabria Italy
- University of Ferrara Italy
Bile Acids and Salts, Solutions, Bile acids; asymmetric synthesis; enclathration; host-guest complexation; enantiomer separation; enantioselective recognition, Humans, Stereoisomerism, Organic Chemicals, Catalysis, Substrate Specificity
Bile Acids and Salts, Solutions, Bile acids; asymmetric synthesis; enclathration; host-guest complexation; enantiomer separation; enantioselective recognition, Humans, Stereoisomerism, Organic Chemicals, Catalysis, Substrate Specificity
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