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Dimerization of Benzyl and Allyl Halides via Photoredox-Mediated Disproportionation of Organozinc Reagents Научная публикация

Журнал Synthesis
ISSN: 1437-210X , E-ISSN: 0039-7881
Вых. Данные Год: 2018, Том: 50, Номер: 15, Страницы: 2930-2935 Страниц : 6 DOI: 10.1055/s-0036-1591583
Авторы Levin Vitalij V. 1 , Agababyan Daniil P. 1 , Struchkova Marina I. 1,2 , Dilman Alexander D. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry
2 D. Mendeleev University of Chemical Technology of Russia, Higher Chemical College

Реферат: Benzyl and allyl halides undergo homocoupling when treated with zinc in the presence of a catalytic amount of a cationic iridium(III) complex under irradiation with 400 nm light-emitting diodes. The reaction proceeds through the intermediate formation of an organozinc reagent, which disproportionates to a free radical and elemental zinc under photoredox conditions.
Библиографическая ссылка: Levin V.V. , Agababyan D.P. , Struchkova M.I. , Dilman A.D.
Dimerization of Benzyl and Allyl Halides via Photoredox-Mediated Disproportionation of Organozinc Reagents
Synthesis. 2018. V.50. N15. P.2930-2935. DOI: 10.1055/s-0036-1591583 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000439116100012
Scopus: 2-s2.0-85047297385
OpenAlex: W2803947532
Цитирование в БД:
БД Цитирований
OpenAlex 20
Scopus 21
Web of science 14
Альметрики: