Photoredox-catalyzed arylation of isonitriles by diaryliodonium salts towards benzamides

Bibliographic Details
Parent link:	Beilstein Journal of Organic Chemistry.— .— Frankfurt am Main: BIACS Vol. 21.— 2025.— P. 1480–1488
Other Authors:	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
Summary:	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
Published:	2025
Subjects:	электронный ресурс труды учёных ТПУ arylation benzamides diaryliodonium salts isonitriles; photoredox
Online Access:	https://doi.org/10.3762/bjoc.21.110
Format:	Electronic Book Chapter
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=681876

Internet

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