General Approach to Amides through Decarboxylative Radical Cross-Coupling of Carboxylic Acids and Isocyanides; Organic Letters; Vol. 26, iss. 16

General Approach to Amides through Decarboxylative Radical Cross-Coupling of Carboxylic Acids and Isocyanides; Organic Letters; Vol. 26, iss. 16

Bibliographic Details
Parent link:	Organic Letters.— .— Washington: ACS Publications Vol. 26, iss. 16.— 2024.— P. 3380–3385
Corporate Author:	Томский политехнический университет
Other Authors:	Qing Yan, Qing-Jia Yuan, Shatskiy A. Andrey, Alvey G. R. Gregory, Stepanova E. V. Elena Vladimirovna, Jian-Quan Liu, Karkas M. D. Markus, Xiang-Shan Wang
Summary:	Title screen Herein, we report a silver-catalyzed protocol for decarboxylative cross-coupling between carboxylic acids and isocyanides, leading to linear amide products through a free-radical mechanism. The disclosed approach provides a general entry to a variety of decorated amides, accommodating a diverse array of radical precursors, including aryl, heteroaryl, alkynyl, alkenyl, and alkyl carboxylic acids. Notably, the protocol proved to be efficient for decarboxylative late-stage functionalization of several elaborate pharmaceuticals, demonstrating its potential applications. Текстовый файл
Language:	English
Published:	2024
Subjects:	труды учёных ТПУ электронный ресурс
Online Access:	https://doi.org/10.1021/acs.orglett.4c00872
Format:	Electronic Book Chapter
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=672791

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