Recent developments in palladium-catalyzed C-S bond formation

被引:106
|
作者
Li, Jianxiao [1 ]
Yang, Shaorong [1 ]
Wu, Wanqing [1 ]
Jiang, Huanfeng [1 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Key Lab Funct Mol Engn Guangdong Prov, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
SULFENYLATED CARBONYL-COMPOUNDS; CROSS-COUPLING REACTION; SULFUR-DIOXIDE; BORONIC ACIDS; STEREOSELECTIVE ADDITION; DIRECTED SULFENYLATION; PROPARGYLIC ALCOHOLS; EFFICIENT SYNTHESIS; CASCADE ANNULATION; TERMINAL ALKYNES;
D O I
10.1039/d0qo00377h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Transition metal-catalyzed C-S bond formation reactions have attracted considerable attention in the recent years. In this regard, palladium-catalyzed C-S bond formation is typically attractive because it can effectively assemble structurally diverse unsymmetrical aryl sulfides and functionalized sulfones under mild conditions with high regioselectivities. In this review, palladium-catalyzed C-S bond formation reactions are summarized and discussed in detail with the focus on sulfenylation and sulfonylation reactions involving aryl/heteroaryl C-H bonds, alkynes, aryl halides, electron-rich benzoic acid derivatives, arylhydrazines, and organosilicon reagents. Some representative synthetic strategies and their transformation application along with reaction mechanisms are also highlighted.
引用
收藏
页码:1395 / 1417
页数:23
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