Issue 3, 1972

Some steroidal 22-enes: the synthesis of (a) steroidal 22,24(28)-dienes and (b) ergosta-5,7,22,24(28)-tetraen-3β-ol

Abstract

Dehydrobromination of 22,23-dibromo-5β-ergostane yields the 22,24(28)-diene; application of this observation furnishes a novel, short route to ergosta-5,7,22,24(28)-tetraen-3β-ol.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 167a-167a

Some steroidal 22-enes: the synthesis of (a) steroidal 22,24(28)-dienes and (b) ergosta-5,7,22,24(28)-tetraen-3β-ol

A. B. Garry, J. M. Midgley, W. B. Whalley and B. J. Wilkins, J. Chem. Soc., Chem. Commun., 1972, 167a DOI: 10.1039/C3972000167A

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