Реферат: Reactions of perfluorinated 1-phenyl-, 1-(2-ethylphenyl)-, 1-(4-ethylphenyl)-, 1-methyl-2-phenyl-, and 1-ethyl-2-phenyl-1,2-dihydrocyclobutabenzenes with iodine in antimony pentafluoride at 130A degrees C, followed by hydroysis of the reaction mixture, resulted in the formation of perfluorinated 2-methyl-, 2-ethyl-2'-methyl-, 4-ethyl-2'-methyl-, 2-ethyl-, and 2-propylbenzophenones via opening of the four-membered ring in the initial cyclobutabenzene at the C-1-C-2 bond. The presence of hydrogen fluoride facilitates the process and promotes profound transformations leading to anthracene derivatives.

Библиографическая ссылка: Mezhenkova T.V. , Karpov V.M. , Platonov V.E.
Opening of the four-membered ring in perfluorinated 1-alkyl-2-phenyl- and 1-aryl-1,2-dihydrocyclobutabenzenes in the system I-2-SbF5
Russian Journal of Organic Chemistry. 2011. V.47. N7. P.1026-1034. DOI: 10.1134/S1070428011070104 WOS Scopus РИНЦ OpenAlex

Оригинальная: Меженкова Т.В. , Карпов В.М. , Платонов В.Е.
Раскрытие четырехчленного цикла перфторированных 1-алкил-2-фенил- и 1-арилбензоциклобутенов в системе I2-SbF5
Журнал органической химии (RUSS J ORG CHEM+). 2011. Т.47. №7. С.1012-1019. РИНЦ

Даты:

Опубликована в печати:	1 июл. 2011 г.
Опубликована online:	6 авг. 2011 г.

Идентификаторы БД:

Web of science:	WOS:000293643600010
Scopus:	2-s2.0-80052398395
РИНЦ:	18003551
OpenAlex:	W2130999543

Цитирование в БД:

БД	Цитирований
Web of science	2
Scopus	2
РИНЦ	2
OpenAlex	2

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