Issue 0, 1980

Dehydrogenation of steroidal and triterpenoid ketones using benzeneseleninic anhydride

Abstract

Steroid and triterpenoid ketones can be smoothly dehydrogenated in high yield with benzeneseleninic anhydride in chlorobenzene at 95–120 °C. With an excess of benzeneseleninic anhydride and longer reaction times 4,4-dimethyl ketones give ring-A-contracted diketones in moderate yield.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1980, 2209-2212

Dehydrogenation of steroidal and triterpenoid ketones using benzeneseleninic anhydride

D. H. R. Barton, D. J. Lester and S. V. Ley, J. Chem. Soc., Perkin Trans. 1, 1980, 2209 DOI: 10.1039/P19800002209

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