Electrooxidative synthesis of 1,2,3-triazolone 1-amines Научная публикация
| Журнал |
Organic & Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539 |
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| Вых. Данные | Год: 2025, Том: 23, Страницы: 4971-4976 Страниц : 6 DOI: 10.1039/d5ob00481k | ||||
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Реферат:
A new method for the synthesis of newly reported heterocycles, namely 1,2,3-triazolone 1-amines, via electrochemically induced intramolecular N–N bond formation was developed. The process involves electrooxidative cyclization of readily available α-aminocarbonyl hydrazones, occurs under mild conditions and enables the preparation of a diverse series of target compounds, although nitrophenyl-substituted substrates undergo decomposition upon electrolysis. Cyclic voltammetry (CV) measurements were also conducted to determine the reaction mechanism and to explain the observed scope limitations. In addition, thermal behavior studies demonstrated moderate thermal stability of several synthesized 1,2,3-triazolone 1-amines in the range of 110–140 °C. Overall, this study represents a promising contribution to the electroorganic synthesis of neglected nitrogen heterocycles for various biomedical and materials science applications.
Библиографическая ссылка:
Titenkova K.
, Chaplygin D.A.
, Fershtat L.L.
Electrooxidative synthesis of 1,2,3-triazolone 1-amines
Organic & Biomolecular Chemistry. 2025. V.23. P.4971-4976. DOI: 10.1039/d5ob00481k WOS Scopus OpenAlex
Electrooxidative synthesis of 1,2,3-triazolone 1-amines
Organic & Biomolecular Chemistry. 2025. V.23. P.4971-4976. DOI: 10.1039/d5ob00481k WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:001478113700001 |
| Scopus: | 2-s2.0-105004019894 |
| OpenAlex: | W4409700340 |