Issue 16, 1975

A cis-perhydroindanone synthesis utilising an intramolecular Diels–Alder reaction

Abstract

An intramolecular Diels–Alder reaction of 2-methylnona-1,6,8-trien-3-one yields cis-2,3,3a,6,7,7a-hexahydro-7a-methylhydrinden-1-one as the major product. The triene is readily synthesised from penta-1,4-dien-3-ol.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 1559-1559

A cis-perhydroindanone synthesis utilising an intramolecular Diels–Alder reaction

J. J. S. Bajorek and J. K. Sutherland, J. Chem. Soc., Perkin Trans. 1, 1975, 1559 DOI: 10.1039/P19750001559

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