Abstract
A general intramolecular Diels–Alder anionic oxy-Cope strategy for the synthesis of tricyclic skeletons and its application to the preparation of the gascardic acid precursor 21 is described. In situ generation of the appropriate cyclopentadiene 9 by isomerization (Et3N) afforded the [4+2] adduct directly or with EtAlCl2 as catalyst. The requisite potassium salt of the 1,5 diene 16 rearranged with concomitant epimerization at 67 °C to the fused ring ketone 18. Selective allylic oxidation and reduction provided 21. Key words: Diels–Alder, oxy-Cope, sesterterpene, synthesis, cycloaddition.

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