Ir-Catalyzed Functionalization of C-H Bonds

被引:72
作者
Choi, Jongwook [1 ]
Goldman, Alan S. [1 ]
机构
[1] Rutgers State Univ, Dept Chem & Chem Biol, New Brunswick, NJ 08903 USA
来源
IRIDIUM CATALYSIS | 2011年 / 34卷
关键词
Alkane metathesis; Borylation; C-H bond activation; Dehydrogenation; Hydroarylation; Iridium catalyst; Silylation; THERMOCHEMICAL ALKANE DEHYDROGENATION; ROOM-TEMPERATURE REACTIONS; SQUARE-PLANAR COMPLEXES; LIGATED IRIDIUM COMPLEX; METAL BORYL COMPLEXES; XPCP PINCER COMPLEXES; SATURATED-HYDROCARBONS; ANTI-MARKOVNIKOV; PHOTOCHEMICAL CARBONYLATION; 5-MEMBERED HETEROARENES;
D O I
10.1007/978-3-642-15334-1_6
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The ability to selectively functionalize C-H bonds holds enormous potential value in virtually every sphere of organic chemistry, from fuels to pharmaceuticals. Transition metal complexes have shown great promise in this context. Iridium provided the first examples of oxidative addition of C-H bonds; this addition is key to iridium's leading role in alkane dehydrogenation and related reactions. Catalysts based on iridium have also proven highly effective for valuable borylations of C-H bonds and, to a lesser extent, for C-Si coupling. Compared with other platinum group metals, iridium chemistry has not been developed as extensively for the elaboration of C-C bonds from C-H bonds, but significant promise is indicated, particularly for coupling with simple hydrocarbons which lack functionalities that can act as directing groups.
引用
收藏
页码:139 / 167
页数:29
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