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Synthesis of New [1,2,5]Chalсogenadiazoles Fused With Pyridine Skeleton and Their Reactions With Neutral C‐Nucleophiles Научная публикация

Журнал Journal of Heterocyclic Chemistry
ISSN: 0022-152X , E-ISSN: 1943-5193
Вых. Данные Год: 2025, Том: 62, Номер: 10, Страницы: 1080-1086 Страниц : 7 DOI: 10.1002/jhet.70053
Авторы Fedorenko Alexey K. 1 , Ivanova Victoria V. 1 , Starosotnikov Alexey M. 1 , Minyaev Mikhail E. 1 , Bastrakov Maxim A. 1
Организации
1 N.D. Zelinsky Institute of Organic Chemistry RAS Moscow Russia

Реферат: Reactions of [1,2,5]oxa- and [1,2,5]selenadiazolo[3,4-c]pyridines with neutral carbon nucleophiles such as indoles, pyrrole, polyphenols, and CH-acids have been studied. All reactions proceed under mild conditions. As a result, a number of complex molecules containing structurally diverse fragments were synthesized, and subsequent oxidative aromatization has been demonstrated.
Библиографическая ссылка: Fedorenko A.K. , Ivanova V.V. , Starosotnikov A.M. , Minyaev M.E. , Bastrakov M.A.
Synthesis of New [1,2,5]Chalсogenadiazoles Fused With Pyridine Skeleton and Their Reactions With Neutral C‐Nucleophiles
Journal of Heterocyclic Chemistry. 2025. V.62. N10. P.1080-1086. DOI: 10.1002/jhet.70053 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001546190200001
Scopus: 2-s2.0-105012625072
OpenAlex: W4413040412
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