Photoredox Activation of Organozinc Reagents: Barbier-Type Reaction of Alkyl Halides with α-(Trifluoromethyl)styrenes

Photoredox Activation of Organozinc Reagents: Barbier-Type Reaction of Alkyl Halides with α-(Trifluoromethyl)styrenes Научная публикация

Журнал

Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052

Вых. Данные

Год: 2021, Том: 23, Номер: 24, Страницы: 9645-9648 Страниц : 4 DOI: 10.1021/acs.orglett.1c03917

Авторы

Gladkov Anton A. ^1,2 , Chernov Grigory N. ^1,2 , Levin Vitalij V. ² , Kokorekin Vladimir A. ² , Dilman Alexander D. ²

Организации

1	Lomonosov Moscow State University, Department of Chemistry, Leninskie Gory 1-3, 119991 Moscow, Russian Federation
2	N. D. Zelinsky Institute of Organic Chemistry, Leninsky prosp. 47, 119991 Moscow, Russian Federation

Organozinc reagents may be activated under blue light irradiation using an organic photocatalyst to generate alkyl radicals. The radicals are trapped by α-(trifluoromethyl)styrenes leading to gem-difluorinated products after elimination of fluoride. The reaction can be conveniently performed under Barbier conditions starting from organic iodides and bromides and elemental zinc.

Gladkov A.A. , Chernov G.N. , Levin V.V. , Kokorekin V.A. , Dilman A.D.
Photoredox Activation of Organozinc Reagents: Barbier-Type Reaction of Alkyl Halides with α-(Trifluoromethyl)styrenes
Organic Letters. 2021. V.23. N24. P.9645-9648. DOI: 10.1021/acs.orglett.1c03917 WOS Scopus OpenAlex

Web of science:	WOS:000744124300059
Scopus:	2-s2.0-85120543525
OpenAlex:	W3217302832

БД	Цитирований
OpenAlex	19
Scopus	19
Web of science	20