Synthesis of the hexahydronaphthalene moiety of (+)-mevinolin

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Abstract

The synthesis of the hexahydronaphthalene moiety (6b) of (+)-mevinolin (1) has been achieved in 10 steps using an intramolecular Diels-Alder reaction of an alkenylallene to set up four of the chiral centers and the diene unit of (6b). © 1983.

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APA

Deutsch, E. A., & Snider, B. B. (1983). Synthesis of the hexahydronaphthalene moiety of (+)-mevinolin. Tetrahedron Letters, 24(35), 3701–3704. https://doi.org/10.1016/S0040-4039(00)94513-1

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