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Electrooxidative cleavage of C1-C2 bonds in acenaphthylene and acenaphthenes Научная публикация

Журнал Electrochimica Acta
ISSN: 1873-3859 , E-ISSN: 0013-4686
Вых. Данные Год: 1997, Том: 42, Номер: 13-14, Страницы: 1933-1941 Страниц : 9 DOI: 10.1016/s0013-4686(97)85464-3
Авторы Ogibin Y.N. 1 , Ilovaisky A.I. 1 , Nikishin G.I. 1
Организации
1 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect 47, 117913 Moscow, Russian Federation

Реферат: The electrooxidative cleavage of C1C2 bonds in acenaphthylene (1), acenaphthene (6), 1-methoxy-(7), 1,1-dimethoxy- (8), and 1,2-dimethoxyacenaphthene (2) resulting from anodic oxidation of these substrates in MeOH is described. The reaction of 1 involves the intermediate formation of 2, and that of 6 and 7 the formation of intermediates 2 and 8 to give 1,8-naphthalenedicarbaldehyde bis(dimethyl acetal) (3), cyclic dimethyl acetal (4), and 1,1,3-trimethoxy-lH,3H-naphtho[1,8-cd]pyran (5) as major final products.
Библиографическая ссылка: Ogibin Y.N. , Ilovaisky A.I. , Nikishin G.I.
Electrooxidative cleavage of C1-C2 bonds in acenaphthylene and acenaphthenes
Electrochimica Acta. 1997. V.42. N13-14. P.1933-1941. DOI: 10.1016/s0013-4686(97)85464-3 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:A1997XA82500002
Scopus: 2-s2.0-0030718112
OpenAlex: W2950651679
Цитирование в БД:
БД Цитирований
OpenAlex 10
Scopus 13
Web of science 7
Альметрики: