DIRECT SYNTHESIS OF g-BUTYROLACTONES VIA g-PHENYL SUBSTITUTED BUTYRIC ACIDS MEDIATED BENZYL RADICAL CYCLIZATION

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2012-11-19

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Synthesis of several g-butyrolactones with aromatic substitution at carbon 5 from comparative g-aryl acids with 25–85% yield are covered. The straight oxidation in the presence of peroxydisulphate-copper(II)chloride system in aqueous medium was applied. The reaction is highly regioselective and leads exclusively to g-butyrolactone, through stable benzylic radical intermediate

Description

Synthesis of several g-butyrolactones with aromatic substitution at carbon 5 from comparative g-aryl acids with 25–85% yield are covered. The straight oxidation in the presence of peroxydisulphate-copper(II)chloride system in aqueous medium was applied. The reaction is highly regioselective and leads exclusively to g-butyrolactone, through stable benzylic radical intermediate

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DIRECT SYNTHESIS OF g-BUTYROLACTONES VIA g-PHENYL SUBSTITUTED BUTYRIC ACIDS MEDIATED BENZYL RADICAL CYCLIZATION

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