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

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dc.contributor.authorN. O. Mahmoodi
dc.contributor.authorM. Jazayri
dc.date.accessioned2012-11-14T14:32:18Z
dc.date.accessioned2025-02-17T14:01:14Z
dc.date.available2012-11-14T14:32:18Z
dc.date.issued2012-11-14
dc.descriptionSynthesis 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 intermediateen_US
dc.description.abstractSynthesis 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 intermediateen_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/4089
dc.language.isoenen_US
dc.subjectDIRECT SYNTHESIS OF g-BUTYROLACTONES VIA g-PHENYL SUBSTITUTED BUTYRIC ACIDS MEDIATED BENZYL RADICAL CYCLIZATIONen_US
dc.titleDIRECT SYNTHESIS OF g-BUTYROLACTONES VIA g-PHENYL SUBSTITUTED BUTYRIC ACIDS MEDIATED BENZYL RADICAL CYCLIZATIONen_US
dc.typeArticleen_US

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