Enabling the Use of Alkyl Thianthrenium Salts in Cross-Coupling Reactions by Copper Catalysis

被引:87
作者
Chen, Cheng [1 ]
Wang, Minyan [1 ]
Lu, Hongjian [1 ]
Zhao, Binlin [3 ]
Shi, Zhuangzhi [1 ,2 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Chem & Biomed Innovat Ctr Chem BIC, Nanjing 210093, Peoples R China
[2] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Henan, Peoples R China
[3] Nanjing Forestry Univ, Coll Sci, Dept Chem & Mat Sci, Nanjing 210037, Peoples R China
基金
中国国家自然科学基金;
关键词
alkynylation; copper; photoredox reactions; radical; sulfonium salts; SONOGASHIRA REACTIONS; ARYLSULFONIUM SALTS; BROMIDES; FUNCTIONALIZATION; BORYLATION; REAGENTS; HALIDES;
D O I
10.1002/anie.202109723
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alkyl groups are one of the most widely used groups in organic synthesis. Here, a a series of thianthrenium salts have been synthesized that act as reliable alkylation reagents and readily engage in copper-catalyzed Sonogashira reactions to build C(sp(3))-C(sp) bonds under mild photochemical conditions. Diverse alkyl thianthrenium salts, including methyl and disubstituted thianthrenium salts, are employed with great functional breadth, since sensitive Cl, Br, and I atoms, which are poorly tolerated in conventional approaches, are compatible. The generality of the developed alkyl reagents has also been demonstrated in copper-catalyzed Kumada reactions.
引用
收藏
页码:21756 / 21760
页数:5
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