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Light-Promoted Allylation of Iododifluoromethylated Alcohols Научная публикация

Журнал European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690
Вых. Данные Год: 2018, Том: 2018, Номер: 27-28, Страницы: 3834-3836 Страниц : 3 DOI: 10.1002/ejoc.201800543
Авторы Panferova Liubov I. 1 , Struchkova Marina I. 1 , Dilman Alexander D. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Leninsky prosp. 47, 119991 Moscow, Russian Federation

Реферат: A method for the synthesis of β,β-difluorinated alcohols by the formal substitution of iodine in the iododifluoromethyl fragment by the allyl group is described. The reaction involves silylation of the starting alcohols with allyl(chloro)dimethylsilane followed by an light-promoted atom transfer process. The C,C-bond-forming event proceeds through 7-endo-trig radical cyclization.
Библиографическая ссылка: Panferova L.I. , Struchkova M.I. , Dilman A.D.
Light-Promoted Allylation of Iododifluoromethylated Alcohols
European Journal of Organic Chemistry. 2018. V.2018. N27-28. P.3834-3836. DOI: 10.1002/ejoc.201800543 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000439775200030
Scopus: 2-s2.0-85050391524
OpenAlex: W2801473988
Цитирование в БД:
БД Цитирований
OpenAlex 8
Scopus 8
Web of science 8
Альметрики: