过渡金属催化C-H活化插羰反应研究进展
谢宁,金朝辉,高华晶,孙健
吉林化工学院 石油化工学院
Advances in Transition Metal-Catalyzed Carbonylative Coupling by C-H Bond Activation
XIE Ning, JIN Zhaohui, GAO Huajing, SUN Jian
摘要
卤代芳烃的插羰反应是合成含羰基化合物的有效途径,使用未被官能化的C-H键实现插羰反应,具有更重要的价值。近年来,过渡金属催化C-H活化的偶联反应备受关注,但C-H键断裂需要很高的能量,对底物的结构和催化剂的类型要求苛刻。本文从反应中使用催化剂类型的角度,综述了过渡金属催化C-H键插羰反应的研究进展。
关键词:
过渡金属
C-H活化
插羰偶联反应
Abstract:
The carbonylative coupling reactions of aryl halides are effective way to synthesize carbonyl compounds. There are more valuable to realize the carbonylative coupling by C-H unactivation. In recent years, transition metal-catalyzed carbonylative coupling reactions have attracted more attention. But more energy will be needed in the cleavage process of C-H and the demands of the structure of substrates and types of catalyst are very harsh. We summarize the advances in transition metal-catalyzed carbonylative coupling by C-H bond activation from the point of the types of catalyst.
Key words:
transition metal
C-H activation
carbonylative coupling
出版日期: 2019-03-25
发布日期: 2019-03-25
整期出版日期: 2019-03-25
引用本文:
谢宁, 金朝辉, 高华晶, 孙健. 过渡金属催化C-H活化插羰反应研究进展
[J]. 吉林化工学院学报, 2019, 36(3): 1-8.
XIE Ning, JIN Zhaohui, GAO Huajing, SUN Jian. Advances in Transition Metal-Catalyzed Carbonylative Coupling by C-H Bond Activation
. Journal of Jilin Institute of Chemical Technology, 2019, 36(3): 1-8.
链接本文:
http://xuebao.jlict.edu.cn/CN/10.16039/j.cnki.cn22-1249.2019.03.001
或
http://xuebao.jlict.edu.cn/CN/Y2019/V36/I3/1
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