Transition-Metal-Catalyzed p-Bond-Assisted C-H Bond Functionalization: An Emerging Trend in Organic Synthesis

被引:158
|
作者
Gandeepan, Parthasarathy [1 ]
Cheng, Chien-Hong [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem, Hsinchu 30013, Taiwan
关键词
annulation; CH activation; directing groups; homogeneous catalysis; transition metals; ONE-POT SYNTHESIS; DIRECT ORTHO-ALKENYLATION; ALKYNYL ARYL ETHERS; REGIOSELECTIVE SYNTHESIS; OXIDATIVE ANNULATION; RHODIUM(III)-CATALYZED SYNTHESIS; ISOQUINOLINIUM SALTS; N-METHOXYBENZAMIDES; ORTHO-OLEFINATION; DIRECTING GROUPS;
D O I
10.1002/asia.201403224
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal-catalyzed CH activation is considered to be an important tool in organic synthesis and has been accepted and widely used by chemists because it is straightforward, cost-effective, and environmentally friendly. A variety of functional groups have been used to direct metal complexes and achieve regioselective CH activation. Most directing is achieved through the sigma-bond coordination of functional groups to the metal catalyst, followed by ortho-selective CH bond cleavage. However, recent work has demonstrated that -coordinating functional groups can also assist in guiding metal complexes for site-selective CH bond activation. This emerging approach significantly expands the scope of CH activation reactions in organic synthesis. Herein, recent developments in this field are summarized.
引用
收藏
页码:824 / 838
页数:15
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