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.

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