Реферат: Perfluorinated 1-ethyl-2-methyl- and 1-isopropyl-2-methyl-1,2-dihydrocyclobutabenzenes reacted with pentafluorobenzene in SbF5 to generate perfluoro(1-ethyl-2-methyl-2-phenyl- and perfluoro(1-izopropyl-2-methyl-2-phenyl-1,2-dihydrocyclobutabenzen-1-yl) cations. These cations in SbF5 at 20A degrees C underwent opening of the four-membered ring and its expansion to five-membered. After hydrolysis, perfluorinated 4-[1-(2-propylphenyl)ethylidene]- and 4-[1-(2-isobutylphenyl)ethylidene]-2,5-cyclohexadien-1-ones were obtained together with perfluoro(3-ethyl- and perfluoro(3-isopropyl-2-phenylinden-1-ones).

Библиографическая ссылка: Mezhenkova T.V. , Sinyakov V.R. , Karpov V.M. , Platonov V.E.
Skeletal transformations of pentafluorophenylation products of perfluorinated 1,2-dialkyl-1,2-dihydrocyclobutabenzenes in SbF5
Russian Journal of Organic Chemistry. 2013. V.49. N10. P.1454-1465. DOI: 10.1134/S1070428013100096 WOS Scopus РИНЦ OpenAlex

Оригинальная: Меженкова Т.В. , Синяков В.Р. , Карпов В.М. , Платонов В.Е.
Скелетные превращения продуктов пентафторфенилирования перфтор-1,2-диалкилбензоциклобутенов в sbf 5
Журнал органической химии (RUSS J ORG CHEM+). 2013. Т.49. №10. С.1476-1487. РИНЦ

Даты:

Опубликована в печати:	1 окт. 2013 г.
Опубликована online:	8 нояб. 2013 г.

Идентификаторы БД:

Web of science:	WOS:000326813100009
Scopus:	2-s2.0-84889027078
РИНЦ:	21896967
OpenAlex:	W1980299742

Цитирование в БД:

БД	Цитирований
Web of science	6
Scopus	5
РИНЦ	5
OpenAlex	6

Альметрики: