Michael additions to steroidal 1-ene-3-ones

Malcolm M. Campbell, Veerappa B. Jigajinni, R. H. Wightman

Research output: Contribution to journalArticle

Abstract

A reactivity pattern was established for Michael addition of aryl thiolates to 17-acetoxy 5a-androst-1-en-3-one. An abnormal bicyclic bridged adduct was obtained in the reaction of thiourea. © 1979.

Original languageEnglish
Pages (from-to)2455-2456
Number of pages2
JournalTetrahedron Letters
Volume20
Issue number26
Publication statusPublished - 1979

Fingerprint Dive into the research topics of 'Michael additions to steroidal 1-ene-3-ones'. Together they form a unique fingerprint.

Cite this