Photoredox-catalyzed arylation of isonitriles by diaryliodonium salts towards benzamides; Beilstein Journal of Organic Chemistry; Vol. 21

Podrobná bibliografie
Parent link:	Beilstein Journal of Organic Chemistry.— .— Frankfurt am Main: BIACS Vol. 21.— 2025.— P. 1480–1488
Další autoři:	Metalnikova N. M. Nadezhda Maksimovna, Antonkin N. S. Nikita Sergeevich, Tuan K. Nguyen, Soldatova N. S. Nataliya Sergeevna, Nyuchev A. V. Alexander, Kinzhalov M. A. Mikhail Andreevich, Postnikov P. S. Pavel Sergeevich
Shrnutí:	Title screen The arylation of isonitriles by diaryliodonium salts under photoredox conditions has been proposed for the first time. The suggested procedure allows preparing a broad range of benzamides using both symmetric and unsymmetric diaryliodonium salts under mild conditions. A plausible mechanism for the reaction and the selectivity of aryl transfer (in case of unsymmetrical iodonium salts) were studied Текстовый файл
Jazyk:	angličtina
Vydáno:	2025
Témata:	электронный ресурс труды учёных ТПУ arylation benzamides diaryliodonium salts isonitriles; photoredox
On-line přístup:	https://doi.org/10.3762/bjoc.21.110
Médium:	Elektronický zdroj Kapitola
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=681876

Internet

https://doi.org/10.3762/bjoc.21.110