Towards Catalytic C-H Activation Using Main Group Elements

被引:0
|
作者
McNally, Andrew [1 ]
机构
[1] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
关键词
C-H activation; main group catalysis; concerted metalation-deprotonation; borylation; phosphenium ions; BOND ACTIVATION; FUNCTIONALIZATION; BORYLATION; CONSTRUCTION; CHEMISTRY; NUMBER;
D O I
10.1055/a-2290-6711
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Catalytic C-H activation reactions are now established as a means to directly transform organic molecules and are commonly associated with metals such as palladium, rhodium, ruthenium and iridium. This Account will describe a short number of reports demonstrating that structures containing main group elements can facilitate C-H activation processes. In particular, boron-based catalysts can promote catalytic arene C-H borylation reactions, and an emerging approach using phosphenium ions can also cleave sp(2) C-H bonds. These processes use a Lewis acidic main group atom combined with a pendant base to cleave C-H bonds, which compares with metal-catalyzed reactions that proceed via concerted metalation deprotonation mechanisms.
引用
收藏
页码:877 / 882
页数:6
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