Autoxidation transformed the N-cyclohexylimine derivative of dibenzyl ketone and of 3,4:5,6-di-benzocyclohepta-3,5-dienone into the corresponding α-ketoketimine(or tautomer) and degraded the intermediate N-cyclohexylimine of benzyl benzoyl ketone into benzoic acid, cyclohexyl isocyanide, cyclohexylamine, and dibenzyl ketone.
K. G. Srinivasan and J. H. Boyer, J. Chem. Soc., Chem. Commun., 1975, 838 DOI: 10.1039/C39750000838
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