Photoredox Promoted Barbier-Type Reaction of Alkyl Iodides with N-Alkyl and N-Aryl Imines

Photoredox Promoted Barbier-Type Reaction of Alkyl Iodides with N-Alkyl and N-Aryl Imines Научная публикация

Журнал

Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263

Вых. Данные

Год: 2023, Том: 88, Номер: 2, Страницы: 1260-1269 Страниц : 10 DOI: 10.1021/acs.joc.2c02598

Авторы

Gladkov Anton A. ^1,2 , Levin Vitalij V. ¹ , Dilman Alexander D. ¹

Организации

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

The reaction of organozinc reagents with unactivated imines is accelerated when performed in the presence of a photocatalyst under blue light irradiation. Coordination between Lewis acidic zinc iodide and the imine is a key factor responsible for the reaction efficiency. The method can be carried out using alkyl iodides under Barbier conditions.

Gladkov A.A. , Levin V.V. , Dilman A.D.
Photoredox Promoted Barbier-Type Reaction of Alkyl Iodides with N-Alkyl and N-Aryl Imines
Journal of Organic Chemistry. 2023. V.88. N2. P.1260-1269. DOI: 10.1021/acs.joc.2c02598 WOS Scopus OpenAlex

Поступила в редакцию:	27 окт. 2022 г.
Опубликована online:	6 янв. 2023 г.

Web of science:	WOS:001038060400001
Scopus:	2-s2.0-85146086516
OpenAlex:	W4313624557

БД	Цитирований
OpenAlex	16
Web of science	16
Scopus	12