Issue 18, 1996

Stereoselective synthesis of petrosterol and a formal synthesis of aragusterols

Abstract

Stereoselective construction of a steroidal side chain containing a 26–27 cyclopropane ring, compound 22, has been achieved by an intramolecular cyclisation of the corresponding β-methylsulfonyloxy cyanide 16, derived from a chiral cyclopentane derivative. Compound 22 has been further utilised in the synthesis of the naturally occurring steroid petrosterol 3.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1996, 2291-2296

Stereoselective synthesis of petrosterol and a formal synthesis of aragusterols

T. Honda, M. Katoh and S. Yamane, J. Chem. Soc., Perkin Trans. 1, 1996, 2291 DOI: 10.1039/P19960002291

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