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

Bibliografiske detaljer
Parent link:	Beilstein Journal of Organic Chemistry.— .— Frankfurt am Main: BIACS Vol. 21.— 2025.— P. 1480–1488
Andre forfattere:	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
Sprog:	engelsk
Udgivet:	2025
Fag:	электронный ресурс труды учёных ТПУ arylation benzamides diaryliodonium salts isonitriles; photoredox
Online adgang:	https://doi.org/10.3762/bjoc.21.110
Format:	Electronisk Book Chapter
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=681876

Beskrivelse
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
DOI:	10.3762/bjoc.21.110

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