2.7- Naphthyridine electrochemical reduction

A spectral study of the electrochemical reduction of 1,5-naphthyridine has been reported.829... 

Special interest was focused on the photochemistry and redox properties of mononuclear ruthenium complexes.20 Examples show the nucleophilic attack of one of the N atoms of 1,8-naphthyridine on the coordinated CO in [Ru(bipy)2(napy)(CO)]2+ upon le reduction of the napy moiety (Scheme 2). Such a type of metallacyclization enables the reduction of the CO group, derived from the electrochemical reduction of C02 catalyzed by [Ru(bipy)(napy)2(CO)2](PF6)2, to produce acetone in the presence of Me4NBF4.21,22 An unusual result is the simultaneous formation of a carbene ligand and the addition of the methoxo group to the naphthyridine ring upon reaction of [Ru(bipy)2(napy)]2+ with propiolic acid in methanol (Scheme 2).23... 

Electrochemical reduction of naphthyridines 1-6 has been reported (1976MI1, 1978MI1). 

---