共 42 条
Site-Selective C-H Functionalization of Arenes Enabled by Noncovalent Interactions
被引:18
作者:

Fernandez-Figueiras, Adolfo
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机构:
Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Sofia 1113, Bulgaria Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Sofia 1113, Bulgaria

Ravutsov, Martin A.
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Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Sofia 1113, Bulgaria Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Sofia 1113, Bulgaria

Simeonov, Svilen P.
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机构:
Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Sofia 1113, Bulgaria
Univ Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, P-1649003 Lisbon, Portugal Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Sofia 1113, Bulgaria
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
来源:
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.
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页码:1 / 10
页数:10
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