Issue 7, 1997

Synthesis and Photochemical Behaviour of 3-(Estran-16-yl)acrylates and 2-(Estran-16-yl)vinyl Ketones†

Abstract

C-16-substituted steroids having an unsaturation in the side chain have been synthesized by sequential Arnold–Vilsmeier and Wittig reactions, subsequent photochemical studies showing the formation of either a dimeric structure or the occurrence of E/Z-isomerization; for one example, treatment with H 2 over Pd–C led to full reduction of the side-chain and ring D.

Article information

Article type
Paper

J. Chem. Res. (S), 1997, 248-249

Synthesis and Photochemical Behaviour of 3-(Estran-16-yl)acrylates and 2-(Estran-16-yl)vinyl Ketones†

T. Thiemann, S. Mataka, M. Tashiro, S. Sasaki and V. Vill, J. Chem. Res. (S), 1997, 248 DOI: 10.1039/A700031F

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