4.3 Article

Asymmetric synthesis of α-unsubstituted β-hydroxy acids

Journal

CURRENT ORGANIC SYNTHESIS
Volume 5, Issue 2, Pages 151-161

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/157017908784221558

Keywords

3-hydroxycarboxylic acids; asymmetric aldol reactions; Reformatsky reactions; asymmetric reduction; Arndt-Eistert homologation; beta-lactones; cyclic sulfites; cyclic sulfates; reductive cleavage

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alpha-unsubstituted beta-hydroxy acids (3-hydroxycarboxylic acids) are constituents of various natural products with pharmacological and other technical properties of interest. They are also important intermediates in organic synthesis. This article reviews various possible routes for asymmetric synthesis of enantiopure or enantiomerically enriched unsubstituted hydroxy acids.

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