DIRECT SYNTHESIS OF g-BUTYROLACTONES VIA g-PHENYL SUBSTITUTED BUTYRIC ACIDS MEDIATED BENZYL RADICAL CYCLIZATION
Date
2012-11-19
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Abstract
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
Keywords
DIRECT SYNTHESIS OF g-BUTYROLACTONES VIA g-PHENYL SUBSTITUTED BUTYRIC ACIDS MEDIATED BENZYL RADICAL CYCLIZATION
