Amide-Directed Tandem C-C/C-N Bond Formation through C-H Activation

被引:249
作者
Zhu, Chen [1 ]
Wang, Rui [1 ]
Falck, John R. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Biochem, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
关键词
amides; annulation; C-C/C-N bond formation; C-H activation; heterocycles; CYCLIN-DEPENDENT KINASES; CARBON-HYDROGEN BONDS; OXIDATIVE CYCLOADDITION; CATALYZED CARBONYLATION; ISOQUINOLONE SYNTHESIS; NITROGEN-HETEROCYCLES; SECONDARY BENZAMIDES; ORGANIC-SYNTHESIS; C(SP(3))-H BONDS; DIRECT ARYLATION;
D O I
10.1002/asia.201200035
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The transformation of C-H bonds into other chemical bonds is of great significance in synthetic chemistry. C-H bond-activation processes provide a straightforward and atom-economic strategy for the construction of complex structures; as such, they have attracted widespread interest over the past decade. As a prevalent directing group in the field of C-H activation, the amide group not only offers excellent regiodirecting ability, but is also a potential C-N bond precursor. As a consequence, a variety of nitrogen-containing heterocycles have been obtained by using these reactions. This Focus Review addresses the recent research into the amide-directed tandem C-C/C-N bond-formation process through C-H activation. The large body of research in this field over the past three years has established it as one of the most-important topics in organic chemistry.
引用
收藏
页码:1502 / 1514
页数:13
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