The anodic oxidation of N-alkyl-lactams occurred regioselectively at the endocyclic carbon atom α to nitrogen in five- and six-membered rings, and at the exocyclic α-carbon atom in seven-membered rings to provide hydroxy-lactams, imides, and dealkylation products.
M. Okita, T. Wakamatsu and Y. Ban, J. Chem. Soc., Chem. Commun., 1979, 749 DOI: 10.1039/C39790000749
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