Photoredox-catalyzed arylation of isonitriles by diaryliodonium salts towards benzamides; Beilstein Journal of Organic Chemistry; Vol. 21
| 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 |
| Language: | English |
| Published: |
2025
|
| Subjects: | |
| 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 |
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