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Photoredox Fluoroalkylation of Hydrazones in Neutral and Reductive Modes Научная публикация

Журнал Advanced Synthesis & Catalysis
ISSN: 1615-4169 , E-ISSN: 1615-4150
Вых. Данные Год: 2021, Том: 363, Номер: 4, Страницы: 1152-1158 Страниц : 7 DOI: 10.1002/adsc.202001381
Авторы van der Worp Boris A. 1,2 , Kosobokov Mikhail D. 2 , Levin Vitalij V. 2 , Dilman Alexander D. 2
Организации
1 Lomonosov Moscow State University Department of Chemistry 119991 Moscow Leninskie Gory 1–3 Russian Federation
2 N. D. Zelinsky Institute of Organic Chemistry, 119991 Moscow, Leninsky prosp. 47, Russian Federation

Реферат: Visible light promoted fluoroalkylation of hydrazones using 4-perfluoropyridine sulfides as fluoroalkyl radical sources is described. The process can proceed in neutral and reductive modes delivering either hydrazones or hydrazines, respectively, depending on structure of starting substrates and reaction conditions. For the reductive process, ascorbic acid is used as a terminal reductant, which recycles the photocatalyst and serves as a source of hydrogen towards nitrogen-centered radicals.
Библиографическая ссылка: van der Worp B.A. , Kosobokov M.D. , Levin V.V. , Dilman A.D.
Photoredox Fluoroalkylation of Hydrazones in Neutral and Reductive Modes
Advanced Synthesis & Catalysis. 2021. V.363. N4. P.1152-1158. DOI: 10.1002/adsc.202001381 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000603453800001
Scopus: 2-s2.0-85098480343
OpenAlex: W3114802650
Цитирование в БД:
БД Цитирований
OpenAlex 24
Scopus 22
Web of science 25
Альметрики: