Palladium-catalyzed convenient synthesis of thioesters from carboxylic acids and disulfides

被引：11

作者：

Xiao, Yong-Mei ^{[1
]}

Zhao, Yu ^{[1
]}

Li, Jia-Qi ^{[1
]}

Yuan, Jin-Wei ^{[1
]}

Yang, Liang-Ru ^{[1
]}

Mao, Pu ^{[1
]}

Mai, Wen-Peng ^{[1
,2
]}

机构：

[1] Henan Univ Technol, Sch Chem & Chem Engn, Zhengzhou 450001, Peoples R China

[2] Henan Univ Engn, Sch Chem & Printing Dyeing Engn, Zhengzhou 450006, Peoples R China

来源：

NEW JOURNAL OF CHEMISTRY | 2023年 / 47卷 / 36期

关键词：

ARYL IODIDES; BOND FORMATION; THIOCARBONYLATION; CARBONYLATION; DERIVATIVES; ALCOHOLS; HALIDES; KETONES; THIOLS; ESTERS;

D O I：

10.1039/d3nj02972g

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A novel palladium-catalyzed convenient synthesis of thioesters from various carboxylic acids and disulfides has been developed. Both aryl and alkyl carboxylic acids are capable of coupling with diaryl or dialkyl disulfides to afford the desirable thioesters in moderate to good yields. This methodology features easy accessibility of starting materials and a broad substrate scope, providing a practical route for thioester synthesis without toxic thiols or CO gas. A novel palladium-catalyzed convenient synthesis of thioesters from various carboxylic acids and disulfides has been developed.

引用

页码：17092 / 17097

页数：6

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