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- W4246141569 abstract "2-Nitro-2′-isothiocyanatobiphenyl was prepared as a new substance, suitable for the investigation of an electrochemically initiated intramolecular cyclization. If it is reduced at a mercury cathode in acidic media an acid catalysed intramolecular follow-up reaction occurs which leads to the formation of 6-mercaptodibenzo (d, f)-(1,3)-diazepin-5-oxide. The rate of the follow-up reaction decreases in neutral or alkaline media and the reduction of the isothiocyanato group also takes place. The main product is here 5,6-dihydrobenzo(c)cinnoline." @default.
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- W4246141569 date "1975-05-25" @default.
- W4246141569 modified "2023-09-25" @default.
- W4246141569 title "Electrochemically initiated intramolecular cyclization of 2-nitro-2′-isothiocyanatobiphenyl" @default.
- W4246141569 doi "https://doi.org/10.1016/0368-1874(75)85079-9" @default.
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