Issue 6, 1978

Steric course of reduction with sodium borohydride of steroidal αβ-epoxy-ketones

Abstract

The formation of cis-and trans-epoxy-alcohols by treatment of steroidal epoxy-ketones with sodium borohydride is analysed in terms of the direction of attack on the corresponding unsubstituted ketones, and the steric hindrance exerted by the epoxide ring.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1978, 568-571

Steric course of reduction with sodium borohydride of steroidal αβ-epoxy-ketones

M. Weissenberg and E. Glotter, J. Chem. Soc., Perkin Trans. 1, 1978, 568 DOI: 10.1039/P19780000568

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