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铑(I)催化的三级膦导向 C-H 芳基化:配体库的快速构建。

Rhodium(I)-Catalyzed Tertiary Phosphine Directed C-H Arylation: Rapid Construction of Ligand Libraries.

机构信息

State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210093, China.

出版信息

Angew Chem Int Ed Engl. 2017 Jun 12;56(25):7233-7237. doi: 10.1002/anie.201703354. Epub 2017 May 15.

Abstract

Modification of commercially available monophosphine ligands with either aryl bromides or chlorides by rhodium(I)-catalyzed, tertiary phosphine directed C-H activation is described. A series of ligand libraries containing mono- and diaryl-substituted groups, having different steric and electronic properties, were obtained in high yields. Based on the outstanding properties of their parent scaffolds, the modified ligands have been found to be powerful in organic reactions.

摘要

通过铑(I)催化、三级膦导向的 C-H 活化,对商业可得的单膦配体进行了芳基溴化物或氯化物的修饰。通过该方法,得到了一系列含有单芳基和二芳基取代基的配体库,这些取代基具有不同的空间和电子性质,产率很高。基于其母体支架的优异性能,发现修饰后的配体在有机反应中非常有效。

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