Photoredox-catalyzed arylation of isonitriles by diaryliodonium salts towards benzamides

التفاصيل البيبلوغرافية
Parent link:	Beilstein Journal of Organic Chemistry.— .— Frankfurt am Main: BIACS Vol. 21.— 2025.— P. 1480–1488
مؤلفون آخرون:	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
الملخص:	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
منشور في:	2025
الموضوعات:	электронный ресурс труды учёных ТПУ arylation benzamides diaryliodonium salts isonitriles; photoredox
الوصول للمادة أونلاين:	https://doi.org/10.3762/bjoc.21.110
التنسيق:	الكتروني فصل الكتاب
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=681876

الوصف
الملخص:	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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