Issue 0, 1974

Structure and absolute stereochemistry of pinguisone

Abstract

Structure (1)(4β,4aβ,7β,7aβ-tetramethyl-4,4a,6,7,7a,8-hexahydrocyclopenta[f]benzofuran-5-one) is definitively assigned to pinguisone on the basis of its mass and 13C n.m.r. spectra; X-ray analysis of its p-bromobenzylidene derivative (4) establishes the absolute stereochemistry of the compound. The simultaneous formation of both (Z)- and (E)-p-bromobenzylidene derivatives (3) and (4) from (1) is discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 1875-1878

Structure and absolute stereochemistry of pinguisone

A. Corbella, P. Gariboldi, G. Jommi, F. Orsini, A. DeMarco and A. Immirzi, J. Chem. Soc., Perkin Trans. 1, 1974, 1875 DOI: 10.1039/P19740001875

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