Issue 15, 1981

Oxygenation of 3-hydroxyflavones by superoxide anion

Abstract

The oxidation of 3-hydroxyflavones by super-oxide anion in the tetrahydrofuran results in oxidative cleavage of the heterocyclic ring to give 2-benzoyloxy-phenylglyoxylic acid without the loss of carbon monoxide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 745-745

Oxygenation of 3-hydroxyflavones by superoxide anion

M. M. A. El-Sukkary and G. Speier, J. Chem. Soc., Chem. Commun., 1981, 745 DOI: 10.1039/C39810000745

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