Issue 0, 1973

Fluorinated sterols. Part I. 26,26,26,27,27,27-Hexafluorodesmosterol

Abstract

The synthesis of hexaflourodesmosrerol (VIII) by a witting condensation between a sterodial triphenylphonium ylide and hexafluoroacetone is described. The 24,25 double bond structure (VIII) is resistant to hydrigenation over palladium and to hydroboration.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1973, 1233-1235

Fluorinated sterols. Part I. 26,26,26,27,27,27-Hexafluorodesmosterol

J. E. Herz and S. C. Montalvo, J. Chem. Soc., Perkin Trans. 1, 1973, 1233 DOI: 10.1039/P19730001233

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