Issue 6, 1986

Cycloaddition route to 14α-formylestrone and derived 14α-substituted products

Abstract

Diels–Alder addition of an ethylene equivalent to steroidal 14,16-dien-17-yl acetates provides a novel synthetic route to 14α-formylestrone, and, hence, to the 14α-hydroxymethyl and 14α-methyl analogues.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 451-453

Cycloaddition route to 14α-formylestrone and derived 14α-substituted products

J. R. Bull and R. I. Thomson, J. Chem. Soc., Chem. Commun., 1986, 451 DOI: 10.1039/C39860000451

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