Issue 10, 1985

Electrochemical reduction of 2-bromo-carboxamides. Self-protonation mechanism and reaction with dimethylformamide

Abstract

Electrochemical reduction of 2-bromo-carboxamides involves self-protonation of the electrogenerated bases and affords, among other products, cyclo-adducts incorporating a dimethylformamide unit.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 660-660

Electrochemical reduction of 2-bromo-carboxamides. Self-protonation mechanism and reaction with dimethylformamide

F. Maran, E. Vianello, G. Cavicchioni and F. D'Angeli, J. Chem. Soc., Chem. Commun., 1985, 660 DOI: 10.1039/C39850000660

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