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Synthesis of both enantiomers of 1-phenylethane-1,2-diol via chirality transfer from bile acid derivatives

Bandyopadhyaya, AK and Sangeetha, NM and Radha, A and Maitra, Uday (2000) Synthesis of both enantiomers of 1-phenylethane-1,2-diol via chirality transfer from bile acid derivatives. In: Tetrahedron: Asymmetry, 11 (17). pp. 3463-3466.

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Official URL: http://dx.doi.org/10.1016/S0957-4166(00)00338-4

Abstract

Both enantiomers of 1-phenylethane-1,2-diol were synthesized with good to excellent enantioselectivities via selective reduction of the phenylglyoxalates derived from bile acids, followed by reductive cleavage. (C) 2000 Elsevier Science Ltd. All rights reserved.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to Elsevier Science.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 09 Sep 2010 11:47
Last Modified: 29 Sep 2010 07:35
URI: http://eprints.iisc.ernet.in/id/eprint/32109

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