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An efficient new synthesis of 5,7-dihydroxy-4-methylisobenzofuran-1(3H)-one, a metabolite of aspergillus flavus and a key intermediate in the synthesis of mycophenolic acid, is reported. The new synthesis involves the preparation of 1,2-dihydro-4,6-dimethoxy-3-methylbenzocyclobuten-1-ol and a regioselective β-scission of alkoxyl radical generated from it with lead tetraacetate as the key steps.
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Kobayashi et al. (1990) studied this question.
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