“…The electroreduction of quinones in DMF, acetonitrile or 1,2‐dichloroethane, under controlled potential conditions and in the presence/absence of benzenediazonium tetrafluoroborate, was described to be an interesting entry to new hydroxy carboxamides, dioxins, cyanomethylated derivatives and other useful compounds . Similarly concomitant electrochemical reduction of a representative o‐quinone scaffold, 9,10‐phenanthrenequinone, and benzenediazonium tetrafluoroborate, using other organic solvents such as chloroform, dichloromethane or chloroacetonitrile led to new coupling products by electrochemically promoted radical pathways that offered wide scope to solvents with labile C‐H bonds. When N ‐methylformamide (NMF) was used as the solvent in the simultaneous reduction of 9,10‐phenanthrenequinone (or 1,10‐phenanthroline‐5,6‐dione) and a diazonium salt, 1,3,4‐oxadiazol‐2(3 H )‐ones and dibenzo[ c,e ]azepines were surprisingly obtained (Figure a).…”