Site-Selective C-H Functionalization of Arenes Enabled by Noncovalent Interactions

被引:18
作者
Fernandez-Figueiras, Adolfo [1 ]
Ravutsov, Martin A. [1 ]
Simeonov, Svilen P. [1 ,2 ]
机构
[1] Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Sofia 1113, Bulgaria
[2] Univ Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, P-1649003 Lisbon, Portugal
关键词
TRANSIENT DIRECTING GROUPS; BORYLATION; META; ACTIVATION; LIGAND; STRATEGY;
D O I
10.1021/acsomega.1c05830
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The direct metal-catalyzed C-H functionalization of arenes has emerged as a powerful tool for streamlining the synthesis of complex molecular scaffolds. However, despite the different chemical environments, the energy values of all C-H bonds are within a fairly narrow range; hence, the regioselective C-H bond functionalization poses a great challenge. The use of covalently bound directing groups is to date the most exploited approach to achieve regioselective C-H functionalization of arenes. However, the required installation and removal of those groups is a serious drawback. Recently, new strategies for regioselective metal-catalyzed distal C-H functionalization of arenes based on noncovalent forces (hydrogen bonds, Lewis acid-base interactions, ionic or electrostatic forces, etc.) have been developed to tackle these issues. Nowadays, these approaches have already showcased impressive advances. Therefore, the aim of this mini-review is to cover chronologically how these groundbreaking strategies evolved over the past decade.
引用
收藏
页码:1 / 10
页数:10
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