Nickel-catalyzed and benzoic acid-promoted direct sulfenylation of unactivated arenes

被引:106
|
作者
Yang, Ke [1 ]
Wang, Yuqi [1 ]
Chen, Xinyong [1 ]
Kadi, Adnan A. [2 ]
Fun, Hoong-Kun [2 ]
Sun, Hao [1 ]
Zhang, Yan [1 ,2 ]
Lu, Hongjian [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Inst Chem BioMed Sci, Nanjing 210093, Jiangsu, Peoples R China
[2] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh 11451, Saudi Arabia
基金
中国国家自然科学基金;
关键词
C-H BOND; COUPLING REACTIONS; DIRECT THIOLATION; C(SP(3))-H BONDS; ARYL HALIDES; COPPER; FUNCTIONALIZATION; ACTIVATION; EFFICIENT; ARYLATION;
D O I
10.1039/c4cc10431e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A nickel-catalyzed and benzoic acid-promoted direct sulfenylation of unactivated arenes using removable 2-(pyridine-2-yl)-isopropylamine as a directing group is described. This strategy provides an efficient access to valuable aryl sulfides with ample substrate scope and a high degree of functional group tolerance.
引用
收藏
页码:3582 / 3585
页数:4
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