The etectroreduction of protic 2-bromoisobutyramides was studied in acetonitrile in the presence of carbon dioxide by means of cyclic voltammetry and controlled-potential electrolysis. The electrogeneration of the α-carbanion is followed by a fast and quantitative carboxylation at the tertiary carbon, despite the NH acidity of the starting compounds. The carboxylate anion was trapped both after and during the electrolysis procedure by ...
[Maran, Flavio; Celadon, Dino; Severin, Maria Gabriella; Vianello, Elio Journal of the American Chemical Society, 1991 , vol. 113, # 24 p. 9320 - 9329]