Modern strategies for C-H functionalization of heteroarenes with alternative coupling partners

被引:86
|
作者
Zhao, Binlin [1 ,2 ]
Prabagar, Baskaran [1 ]
Shi, Zhuangzhi [1 ]
机构
[1] Nanjing Univ, Chem & Biomed Innovat Ctr ChemB, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Nanjing 210093, Peoples R China
[2] Nanjing Forestry Univ, Coll Sci, Dept Chem & Mat Sci, Nanjing 210037, Peoples R China
来源
CHEM | 2021年 / 7卷 / 10期
基金
中国国家自然科学基金;
关键词
PYRIDINIUM SALTS; CARBOXYLIC-ACIDS; DIRECT C2-ARYLATION; NICKEL CATALYSIS; DIRECT ARYLATION; BOND ARYLATION; N-HETEROARENES; ARYL; ALKYLATION; AZOLES;
D O I
10.1016/j.chempr.2021.08.001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heteroarenes containing oxygen, nitrogen, and/or sulfur are important in numerous aspects of chemistry and everyday life. C-H functionalization of heteroarenes represents the fastest and most atom- economical approach for the synthesis of complex molecules. This strategy avoids the requirement of de novo synthesis and is beneficial for the late-stage modification of structurally complex molecules. Although early protocols for C-H functionalization using organic halides (I, Br, and Cl) as coupling partners remain in active use today, a range of modern strategies allows the cleavage of less reactive C-Het (F, O, S, N, and P) and C-C bonds to form essential links to the feedstock chemicals, highlighting their renewable and sustainable features. This review focuses on modern strategies for the C-H functionalization of heteroarenes with these alternative coupling partners. Most of the transformations can be achieved through catalytic processes. Some non-catalytic strategies involving new reagents and techniques are also introduced.
引用
收藏
页码:2585 / 2634
页数:50
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