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

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

Detaylı Bibliyografya
Parent link:	Beilstein Journal of Organic Chemistry.— .— Frankfurt am Main: BIACS Vol. 21.— 2025.— P. 1480–1488
Diğer Yazarlar:	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
Özet:	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
Dil:	İngilizce
Baskı/Yayın Bilgisi:	2025
Konular:	электронный ресурс труды учёных ТПУ arylation benzamides diaryliodonium salts isonitriles; photoredox
Online Erişim:	https://doi.org/10.3762/bjoc.21.110
Materyal Türü:	Elektronik Kitap Bölümü
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=681876

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