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Electrochemical cleavage of bridged C-C bonds in bicyclic enol ethers and monooxa- and dioxabicycloalkanes: An approach to macrocyclic compounds Научная публикация

Журнал Russian Journal of Electrochemistry
ISSN: 1023-1935 , E-ISSN: 1608-3342
Вых. Данные Год: 2000, Том: 36, Номер: 2, Страницы: 193-202 Страниц : 10 DOI: 10.1007/bf02756906
Авторы Ogibin Yu.N. 1 , Terent’ev A.O. 1 , Ilovaiskii A.I. 1 , Nikishin G.I. 1
Организации
1 Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 117913, Moscow, Russia

Реферат: Electrolysis of bicyclic enol ethers in methanol results in their electrochemical mono-and dimethoxylation. Electrolysis of monooxa-and dioxabicycloalkanes leads to the electrochemical cleavage of their bridged C-C bonds and electrooxidative conversion into esters of Ω-(2-methoxytetrahydrofuryl)-, Ω-(dimethoxymethyl)-, and Ω-(l,3-dioxalan-2-yl) alkanoic acids.
Библиографическая ссылка: Ogibin Y.N. , Terent’ev A.O. , Ilovaiskii A.I. , Nikishin G.I.
Electrochemical cleavage of bridged C-C bonds in bicyclic enol ethers and monooxa- and dioxabicycloalkanes: An approach to macrocyclic compounds
Russian Journal of Electrochemistry. 2000. V.36. N2. P.193-202. DOI: 10.1007/bf02756906 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000086098700015
Scopus: 2-s2.0-0033807247
OpenAlex: W2005711362
Цитирование в БД:
БД Цитирований
OpenAlex 1
Scopus 1
Web of science 1
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