Diastereoselective reduction of α-keto esters derived from functionalised cholic acid

Maltra, U and Packiarajan, M (1994) Diastereoselective reduction of α-keto esters derived from functionalised cholic acid. In: Tetrahedron: Asymmetry, 5 (7). 1171 -1174 .

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Abstract

The reduction of phenylglyoxalate 2a and pyruvate 2b with LiBH4 in THF at -80 degrees C yield the corresponding alpha-hydroxy esters with ca. 70% diastereoselectivity.

Item Type:	Editorials/Short Communications
Publication:	Tetrahedron: Asymmetry
Publisher:	Elsevier Science
Additional Information:	Copyright of this article belongs to Elsevier Science.
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	02 Jun 2011 05:58
Last Modified:	02 Jun 2011 05:58
URI:	http://eprints.iisc.ac.in/id/eprint/36405

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