Ni-Catalyzed Aryl Thioester Synthesis via Thioester Transfer Reaction

被引:0
作者
Liang, Luqi [1 ]
Xi, Juan [1 ]
Jiang, Ruonan [1 ]
Yang, Yi [1 ]
Sun, Fenggang [1 ]
Zhang, Lizhi [1 ]
Li, Xinjin [1 ]
Liu, Hui [1 ]
机构
[1] Shandong Univ Technol, Sch Chem Engn, Zibo 255049, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Ni-catalysis; thioester; oxidative addition; HIGHLY REGIOSELECTIVE THIOCARBONYLATION; CARBON-MONOXIDE; PALLADIUM COMPLEXES; EFFICIENT SYNTHESIS; 1ST EXAMPLES; THIOLS; CARBONYLATION; ALCOHOLS; HALIDES; ESTERIFICATION;
D O I
10.6023/cjoc202208035
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A nickel-catalyzed thioester transfer reaction using thioesters and aryl iodides was realized, utilizing simple and readily available thioesters as the sulfur source without smelly thiols and toxic carbon monoxide gas. The thioester transfer reaction involves two oxidative additions with Ni(0): C-S bond of the aromatic ester and C-I bond of haloarenes, and the two resulting intermediates undergoe a functional group exchange reaction to afford the new thioester. Furthermore, this approach features mild conditions and operational simplicity, providing a practical route for thioester synthesis.
引用
收藏
页码:1566 / 1573
页数:8
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