Michael additions to steroidal 1-ene-3-ones

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

Research output: Contribution to journalArticle


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
Issue number26
Publication statusPublished - 1979

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    Campbell, M. M., Jigajinni, V. B., & Wightman, R. H. (1979). Michael additions to steroidal 1-ene-3-ones. Tetrahedron Letters, 20(26), 2455-2456.