Design of Highly Enantioselective Organocatalysts Based on Molecular Recognition
Organic Letters2006Vol. 8(7), pp. 1263–1266
Citations Over TimeTop 10% of 2006 papers
Abstract
[reaction: see text] Various organocatalysts have been designed based on molecular recognition to catalyze the asymmetric direct aldol reaction of ketones with aryl and alkyl alpha-keto acids, affording beta-hydroxyl carboxylic acids with a tertiary stereogenic center with excellent enantioselectivities of up to 98% ee. A linear effect was observed for the reaction, demonstrating a single molecule of the catalyst involved in the catalysis.
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