Transition metal-catalyzed cross-coupling reactions of N-aryl-2-aminopyridines

被引：1
|
作者：
Doraghi, Fatemeh [1 ]
Rezainia, Lina [2 ]
Morshedsolouk, Mohammad Hossein [1 ,2 ]
Navid, Hamed [2 ]
Larijani, Bagher [1 ]
Mahdavi, Mohammad [1 ]
机构：
[1] Univ Tehran Med Sci, Endocrinol & Metab Clin Sci Inst, Endocrinol & Metab Res Ctr, Tehran, Iran
[2] Univ Tehran, Coll Sci, Sch Chem, Tehran, Iran
来源：
RSC ADVANCES | 2025年 / 15卷 / 02期
关键词：
C-H ACTIVATION; ANNULATION; FUNCTIONALIZATION; AMINATION; ALKYNES; ACCESS; ARENES;
D O I：
10.1039/d4ra08384a
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Due to the presence of the pyridyl directing group, N-aryl-2-aminopyridines can quickly form stable complexes with metals, leading to cyclization and functionalization reactions. A large number of N-heterocycles and nitrogen-based molecules can be easily constructed via this direct and atom-economical cross-coupling strategy. In this review, we have highlighted the transformations of N-aryl-2-aminopyridines in the presence of various transition metal catalysts, such as palladium, rhodium, iridium, ruthenium, cobalt and copper.
引用
收藏
页码：1134 / 1151
页数：18
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