Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 11, Pages 1450-1452Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b417267a
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The asymmetric direct aldol reactions of a wide scope of aldehydes with unmodified ketones in the presence of 20 mol% (S, S, S)-pyrrolidine-2-carboxylic acid (2'-hydroxyl-1',2'-diphenylethyl)- amine ( 1) were performed in ionic liquids; aldol products with 91 to >99% ees for aromatic aldehydes and 99% ees for alphatic aldehydes were offered by the present procedure.
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