Transition metal-catalyzed direct borylation and silylation based on C-H activation

被引:21
作者
Ishiyama, T [1 ]
机构
[1] Hokkaido Univ, Grad Sch Engn, Div Mol Chem, Sapporo, Hokkaido 0608628, Japan
关键词
C-H activation; transition metal catalyst; hydrocarbon; borylation; silylation; organoboron compound; organosilicon compound;
D O I
10.5059/yukigoseikyokaishi.63.440
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Direct borylation and silylation of unreactive C-H bonds catalyzed by transition metal complexes have been extensively studied by several research groups and have become economical, efficient, elegant, and environmentally benign protocols for the synthesis of a variety of organoboron and organosilicon compounds. A number of transition metal complexes catalyzes C-H borylation and silylation of alkanes, arenes, heteroarenes, alkenes, or benzylic positions of alkylarenes by diborons or hydoroboranes and disilanes or hydrosilanes to produce the corresponding alkyl-, aryl-, heteroaryl-, vinyl-, or benzylboron and -silicon compounds, respectively. In this review, seminal early works and exciting recent developments in the area of direct borylation and silylation of hydrocarbons based on C-H activation are summarized.
引用
收藏
页码:440 / 452
页数:13
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