Issue 0, 1971

Seco-steroids. Part I. 15,16-Secoprogesterone

Abstract

The synthesis of the title compound via its C-17 epimer is described. Key steps are the cleavage of a 16,17-dihydroxy-D-homoandrostane derivative followed by decarbonylation of the aldehyde formed. Several of the D-homoandrostane intermediates show anomalous n.m.r. spectra.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 2491-2495

Seco-steroids. Part I. 15,16-Secoprogesterone

N. S. Crossley, J. Chem. Soc. C, 1971, 2491 DOI: 10.1039/J39710002491

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