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Electrooxidative synthesis of 1,2,3-triazolone 1-amines Научная публикация

Журнал Organic & Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539
Вых. Данные Год: 2025, Том: 23, Страницы: 4971-4976 Страниц : 6 DOI: 10.1039/d5ob00481k
Авторы Titenkova Kseniia 1,2 , Chaplygin Daniil A. 2 , Fershtat Leonid L. 2
Организации
1 Department of Chemistry, Moscow State University, 119991 Leninskie Gory 1-3, Moscow, Russia
2 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991, Leninsky Prosp., 47, Moscow, Russia

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
Идентификаторы БД:
Web of science: WOS:001478113700001
Scopus: 2-s2.0-105004019894
OpenAlex: W4409700340
Цитирование в БД:
БД Цитирований
OpenAlex 4
Web of science 4
Scopus 3
Альметрики: