Metal-Free Oxidative C-C Bond Formation through C-H Bond Functionalization

被引:154
作者
Narayan, Rishikesh [1 ]
Matcha, Kiran [1 ]
Antonchick, Andrey P. [1 ,2 ]
机构
[1] Max Planck Inst Mol Physiol, Abt Chem Biol, D-44227 Dortmund, Germany
[2] Tech Univ Dortmund, Fak Chem & Chem Biol, D-44221 Dortmund, Germany
关键词
C-C coupling; C-H activation; hypervalent iodine; metal-free; oxidative coupling; HYPERVALENT IODINE(III) REAGENT; BIARYL COUPLING REACTION; CARBON-HYDROGEN BONDS; N-ARYL ENAMINES; TERTIARY-AMINES; ORGANIC-SYNTHESIS; PHENYLIODINE(III) BIS(TRIFLUOROACETATE); NUCLEOPHILIC-SUBSTITUTION; AEROBIC CONDITIONS; CATALYTIC AMOUNTS;
D O I
10.1002/chem.201502005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The formation of C-C bonds embodies the core of organic chemistry because of its fundamental application in generation of molecular diversity and complexity. C-C bond-forming reactions are well-known challenges. To achieve this goal through direct functionalization of C-H bonds in both of the coupling partners represents the state-of-the-art in organic synthesis. Oxidative C-C bond formation obviates the need for prefunctionalization of both substrates. This Minire-view is dedicated to the field of C-C bond-forming reactions through direct C-H bond functionalization under completely metal-free oxidative conditions. Selected important developments in this area have been summarized with representative examples and discussions on their reaction mechanisms.
引用
收藏
页码:14678 / 14693
页数:16
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