| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 66416 | Journal of Molecular Catalysis A: Chemical | 2011 | 5 Pages |
Abstract
Ni(OAc)2·4H2O could catalyze direct C–H arylation of unactivated arenes with aryl halides in presence of 1,10-phenanthroline without using additives.
Graphical abstractReadily available Ni(OAc)2·4H2O could catalyze direct C–H arylation of unactivated arenes with aryl bromides/iodides in presence of 1,10-phenanthroline as the ligand without using any additives. This protocol makes C–H arylation more practical and useful.Figure optionsDownload full-size imageDownload high-quality image (100 K)Download as PowerPoint slideHighlights► Direct C–H arylation. ► Coupling of unactivated arenes with aryl halides. ► Readily available Ni(OAc)2·4H2O. ► Without using any additives.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Guanlei Xie, Tingyi Li, Xiaoming Qu, Jincheng Mao,