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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.
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页码:1395 / 1417
页数:23
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