Issue 16, 1983

Electrochemical oxidation of aromatic enediamines. A unique example of anodic double cyclisation to an indolo-oxazolidine

Abstract

The anodic oxidation of enediamines leads to an unexpected cyclisation involving solvent moisture to give an indolo-oxazolidine in a good yield.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 876-877

Electrochemical oxidation of aromatic enediamines. A unique example of anodic double cyclisation to an indolo-oxazolidine

M. Cariou, R. Carlier and J. Simonet, J. Chem. Soc., Chem. Commun., 1983, 876 DOI: 10.1039/C39830000876

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