Palladium-Catalyzed C-C Bonds Formation Reactions via Selective C-H Bonds Functionalization

被引:0
作者
Li Hu [1 ]
Shi Zhangjie [1 ,2 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Key Lab Bioorgan Chem & Mol Engn, Minist Educ,BNLMS, Beijing 100871, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
关键词
palladium-catalyzed; C-H bonds functionalization; directed; selective; cross-coupling reaction; CROSS-COUPLING REACTIONS; PROTON-ABSTRACTION MECHANISM; DIRECT C-2 ARYLATION; ORGANOMETALLIC CHEMISTRY; ROOM-TEMPERATURE; N-OXIDES; ORGANOTIN REAGENTS; ORTHO-ALKYLATION; ARYL HALIDES; ACTIVATION;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In past decades, palladium-catalyzed direct selective C-H bonds functionalization has become a highly attractive strategy in organic synthesis and represents a highly desirable goal. This review introduces three extensively investigated modes for forming C-C bonds from C-H bonds via palladium catalysis; cross-coupling reactions of C-H bonds with aryl or alkyl halides/pseudohalides, cross-dehydrogenative couplings of two C-H bonds, and cross-coupling reactions of C-H bonds with organometallic reagents. A comprehensive summary of recent advances and detailed analysis on the versatility and practicality of these transformations are presented. The research trend for this strategy is also prospected.
引用
收藏
页码:1414 / 1433
页数:20
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