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Selective Electrochemical Hydrocarboxylation of Vinyl Phosphonates with CO 2 Enabled by Alternating Polarity Научная публикация

Журнал Advanced Synthesis & Catalysis
ISSN: 1615-4169 , E-ISSN: 1615-4150
Вых. Данные Год: 2026, Том: 368, Номер: 11, Номер статьи : e70559, Страниц : DOI: 10.1002/adsc.70559
Авторы Ustyuzhanin Alexander O. 1 , Podgornaia Polina A. 1 , Kolotyrkina Natalia G. 1 , He Liang‐Nian 2 , Vil’ Vera A. 1 , Terent’ev Alexander O. 1
Организации
1 N.D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences Moscow Russian Federation
2 State Key Laboratory and Institute of Elemento‐Organic Chemistry College of Chemistry Nankai University Tianjin China

Реферат: Electrochemical hydrocarboxylation of vinyl phosphonates with CO2 to form carboxylic-substituted phosphonates is developed. The alternating polarity affords a boost in Faraday efficiency and enables generalizable catalytic control to provide high product yields over a broad substrate scope by maintaining electrode activity through the regeneration of its surface. The disclosed method provides high selectivity of the target hydrocarboxylation without side transformations of vinyl phosphonates in an undivided cell affording a short way to valuable carboxylic acids featuring a phosphonate fragment. The high selectivity of hydrocarboxylation is achieved through the integration of an alternating polarity strategy with an efficient sequence of one-electron reduction, followed by CC bond formation, subsequent second one-electron reduction, and protonation. These results establish the utility of the alternating polarity technique and provide a foundation for its adaptation to other electrochemical reactions.
Библиографическая ссылка: Ustyuzhanin A.O. , Podgornaia P.A. , Kolotyrkina N.G. , He L. , Vil’ V.A. , Terent’ev A.O.
Selective Electrochemical Hydrocarboxylation of Vinyl Phosphonates with CO 2 Enabled by Alternating Polarity
Advanced Synthesis & Catalysis. 2026. V.368. N11. e70559 . DOI: 10.1002/adsc.70559 OpenAlex
Даты:
Поступила в редакцию: 3 мар. 2026 г.
Опубликована online: 28 мая 2026 г.
Идентификаторы БД:
≡ OpenAlex: W7162654783
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