Author:
Buckley DG,Ritchie E,Cooks RG
Abstract
3-Acetyl- and
3-benzoyl-phthalides have been synthesized. The former was stable to alkaline
degradation but the latter yielded phthalide and benzoic acid, together with
other products. The results support the mechanism previously proposed for the
base-induced conversion of radicicol dimethyl ether into the corresponding
phthalide. Attempts to prepare 3-p-nitrobenzoylphthalide are described.
Cited by
13 articles.
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