Аннотация:
Electrochemical reduction of ortho-piperidino substituted nitro(het)arenes in an undivided cell on a lead cathode in 8% HCl gave either 1,2,3,4-tetrahydropyrido[1,2-a]-benzimidazoles or 6,7,8,9-tetrahydropyrido[3′,2′:4,5]- imidazo[1,2-a]pyridines. The reductive heterocyclization mechanism involves the initial formation of a nitroso derivative followed by the formation of an imidazole ring.
Образец цитирования:
R. S. Begunov, V. O. Sakulina, M. A. Syroeshkin, E. A. Saverina, A. A. Sokolov, M. E. Minyaev, “Electroreductive heterocyclization of ortho-piperidino substituted nitro(het)arenes”, Mendeleev Commun., 30:5 (2020), 633–635
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1276
https://www.mathnet.ru/rus/mendc/v30/i5/p633
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R. S. Begunov, Yu. V. Zaitseva, A. A. Sokolov, D. O. Egorov, S. I. Filimonov, “Synthesis and Antibacterial Activity of 1,2,3,4-Tetrahydro- and Pyrido[1,2-a]Benzimidazoles”, Pharm Chem J, 56:1 (2022), 22
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