Recent Progress in the Development of Multitasking Directing Groups for Carbon-Hydrogen Activation Reactions

被引:44
|
作者
Sun, Huan [1 ]
Huang, Yong [1 ]
机构
[1] Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Key Lab Chem Genom, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon-hydrogen activation; directing groups; multitasking functional groups; transition metals; substituted heterocycles; C-H ACTIVATION; CROSS-COUPLING REACTION; N BOND FORMATION; EFFICIENT SYNTHESIS; INDOLE SYNTHESIS; REGIOSELECTIVE SYNTHESIS; RHODIUM(III)-CATALYZED SYNTHESIS; STRUCTURAL DIVERSITY; O BOND; PALLADIUM;
D O I
10.1055/s-0035-1560169
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Selective carbon-hydrogen activation reactions can be accomplished in a predictive manner using directing auxiliaries. However, the majority of directing groups discovered to date are difficult to remove or to transform into a desirable functionality. Recently, removable, cleavable, and redox-neutral directing groups have been developed that significantly broaden both the substrate scope and synthetic diversity of carbon-hydrogen functionalization reactions. In this short account, we summarize recent progress we have made in the development of multitasking (removable, cleavable, redox-neutral, manipulable) directing groups for carbon-hydrogen activation reactions. 1 Introduction 2 Triazene 3 Nitrous Amide 4 Pyrazolidinone 5 N-Oxyacetamide 6 Conclusion
引用
收藏
页码:2751 / 2762
页数:12
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