Primary amides: Sustainable weakly coordinating groups in transition metal-catalyzed C-H bond functionalization reactions

被引:14
|
作者
Thakur, Rima [1 ]
Jaiswal, Yogesh [2 ]
Kumar, Amit [2 ]
机构
[1] Natl Inst Technol Patna, Dept Chem, Patna 800005, Bihar, India
[2] Indian Inst Technol Patna, Dept Chem, Bihta 801106, Bihar, India
关键词
Primary amide as a directing group; C-H activation; functionalization; Catalysis; N-heterocycles; Transition-metal salts (Pd; Rh; Ru); TRANSIENT DIRECTING GROUPS; PRIMARY BENZAMIDES; DIAZO-COMPOUNDS; SITE-SELECTIVITY; CARBOXYLIC-ACIDS; DIRECT ARYLATION; ARYL HALIDES; ACTIVATION; CYCLIZATION; ACCESS;
D O I
10.1016/j.tet.2021.132313
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The directing groups assisted transition-metal catalyzed functionalization of unreactive C-H bond is considered as one of the valuable alternative synthetic tools to the conventional organic synthesis. The significant challenges in these fields are the requirements of two extra steps: introduction and removal of the directing group. Therefore, recently specific attention has been paid to utilize the useful functional motifs as desired directing groups for the site-selective activation of C-H bonds. Primary amides are considered as one of the fundamental functional groups that play an essential role in chemistry and biology. The presence of N and O atoms in amides makes them an ideal substrate for the directing group in transition-metal catalyzed C-H activation reactions. In this report, we give a brief overview of the recent development of primary amides as sustainable coordinating directing groups for the site-selective activation of ortho-C-H bonds of aromatic compounds followed by annulation reactions to make different molecular architectures. (c) 2021 Elsevier Ltd. All rights reserved.
引用
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页数:26
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