Abstract
Sclerotinin A (3, 6, 8-trihydroxy-3, 4, 5, 7-tetramethyl-3, 4-dihyroisocoumarin: 1), a metabolite of Scierotinia sclerotiorum, was first totally synthesized. The pentenone ring of 2, 3, 4, 6-tetramethyl-5, 7-dimethoxyindanone (VIIa) which was obtained from 2, 4-dimethylresorcinol dimethyl ether (VI) through a new synthetic process, was cleavaged oxidatively, and demethylated to I. Sclerotinin A was also yielded from indanone dibenzyl ether (VIIb) by the same method and reductive debenzylation.
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