Free Amine, Hydroxyl and Sulfhydryl Directed C-H Functionalization and Annulation: Application to Heterocycle Synthesis

被引:15
作者
Kumar, Sandeep [1 ,2 ,3 ]
Kumar, Akshay [1 ]
Sharma, Dharminder [2 ,4 ]
Das, Pralay [2 ,3 ]
机构
[1] DAV Univ, Dept Chem, Jalandhar 144012, Punjab, India
[2] CSIR Inst Himalayan Bioresource Technol, Chem Technol Div, Palampur 176061, HP, India
[3] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
[4] JCDAV Coll Dasuya, PG Dept Chem, Chandigarh 144205, Punjab, India
关键词
annulation; C-H activation; heterocycles; native; transition metals; ONE-POT SYNTHESIS; NITROGEN-CONTAINING HETEROCYCLES; REGIOSELECTIVE SYNTHESIS; ORTHOGONAL SELECTIVITY; BOND FUNCTIONALIZATION; OXIDATIVE ANNULATION; CASCADE REACTIONS; O-ARYLANILINES; ACTIVATION; ALKENYLATION;
D O I
10.1002/tcr.202100171
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal-catalyzed direct C-H bond functionalization is recognized as an efficient strategy to assemble heterocyclic frameworks. For this purpose, directing groups (DGs) installation on an organic molecule has remained a widely exploited strategy for the years. The installation of directing groups, especially for the amine, alcohol and thiol containing reactants and their removal after the reaction need additional steps. In this regard, the use of free amine, hydroxyl and sulfhydryl as directing groups in native form is advantageous and in recent times, these transformations have stirred undisputable advancements for applications to heterocycle synthesis. In this review, the aromatic sp(2)-C attached free amine, hydroxyl and sulfhydryl as native functionalities are shown to be useful for the construction of five to seven-membered N-, O- and S-heterocycles.
引用
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页数:30
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