Реферат: The reactions of perfluoro-2-methyl-2-pentene with substituted phenols and some heterocyclic compounds containing, OH group result in the substitution of the fluorine atom either exclusively at the internal multiple bond or at the terminal multiple bond of perfluoro-2-methyl- I -pentene formed by isomerization of the starting, perfluoroolefin in the course of the reaction. The reaction pathway depends on the reaction conditions, base used, and substituents in the benzene ring. The structures of the compounds were confirmed by H-1, C-13, and F-19 NMR and IR spectroscopy.

Библиографическая ссылка: Furin G.G. , Zhuzhgov E.L. , Chi K.-V. , Kim N.-A.
Synthesis of partially fluorinated organic compounds from perfluoro-2-methyl-2-pentene and phenol derivatives
Russian Journal of General Chemistry. 2005. V.75. N3. P.394-401. DOI: 10.1007/s11176-005-0238-6 WOS Scopus РИНЦ OpenAlex

Оригинальная: Фурин Г.Г. , Жужгов Э.Л. , Chi K.-. , Kim N.-.
Синтез частично фторированных органических соеди нений с использованием перфтор-2-метил-2-пентена и производных фенола
Журнал общей химии (RUSS J GEN CHEM+). 2005. Т.75. №3. С.430-437. РИНЦ

Даты:

Опубликована в печати:

1 мар. 2005 г.

Идентификаторы БД:

Web of science:	WOS:000229691000015
Scopus:	2-s2.0-24644479628
РИНЦ:	13486258
OpenAlex:	W1990335500

Цитирование в БД:

БД	Цитирований
Web of science	3
Scopus	3
РИНЦ	3
OpenAlex	2

Альметрики: