Issue 22, 1975

Studies on steroids. Part XXIX. Synthesis of allenic analogues of fucosterol and desmosterol

Abstract

As potential specific inhibitors of sterol biosynthesis, two steroidal allenes, stigmasta-5,24(28),28-trien-3β-ol (6) and cholesta-5,23,24-trien-3β-ol (22), have been synthesized via a reductive SN2′ reaction(lithium aluminium hydride–aluminium chloride) of the corresponding αβ-acetylenic alcohols.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 2302-2307

Studies on steroids. Part XXIX. Synthesis of allenic analogues of fucosterol and desmosterol

Y. Fujimoto, M. Morisaki and N. Ikekawa, J. Chem. Soc., Perkin Trans. 1, 1975, 2302 DOI: 10.1039/P19750002302

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