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Electrochemical transformations of monooxa- and dioxabicycloalkenes and-bicycloalkanes Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 1999, Том: 48, Номер: 11, Страницы: 2091-2099 Страниц : 9 DOI: 10.1007/bf02494854
Авторы Ogibin Yu.N. 1 , Terent'ev A.O. 1 , Ilovaisky A.I. 1 , Nikishin G.I. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Реферат: Electrolysis of 2-oxa- and 2,5-dioxabicyclo[n.4.0]alk-1(6)0enes (n=4, 10) under conditions of direct undivided anodic oxidation in methanol results in their electrochemical mono-and dimethoxylation; electrolysis of the corresponding 2-oxa-and 2,5-dioxabicycloalkanes involves electrochemical cleavage of the bridging carbon—carbon bonds followed by electrooxidative transformation into methyl ω-(2-methoxytetrahydrofuryl)-, ω-(dimethoxy-methyl)-, and ω-(1,3-dioxolan-2-yl)alkanoates.
Библиографическая ссылка: Ogibin Y.N. , Terent'ev A.O. , Ilovaisky A.I. , Nikishin G.I.
Electrochemical transformations of monooxa- and dioxabicycloalkenes and-bicycloalkanes
Russian Chemical Bulletin. 1999. V.48. N11. P.2091-2099. DOI: 10.1007/bf02494854 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000084420700016
Scopus: 2-s2.0-0033235437
OpenAlex: W1993080143
Цитирование в БД:
БД Цитирований
OpenAlex 4
Scopus 2
Web of science 3
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