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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1994 Volume 4, Issue 1, Pages 11–12 (Mi mendc5130)

This article is cited in 1 paper

A Highly Regio- and Stereoseiective Reduction of Steroidal 3′(2H)-Furanone

V. A. Khripach, M. I. Zavadskaya, O. A. Drachenova, G. P. Fando

Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus, Minsk, Belarus

Abstract: The reduction of steroidal 3′(2H)-furanone under the action of complex hydrides yields, regio- and stereoselectively in high yield, the corresponding tetrahydrofuranol, which has value as a potential intermediate in the synthesis of steroids containing polyhydroxylated side chains.

Language: English

DOI: 10.1070/MC1994v004n01ABEH000326



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