| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 67103 | Journal of Molecular Catalysis A: Chemical | 2009 | 5 Pages |
The first heterogeneous carbonylative Sonogashira coupling reaction of terminal alkynes with aryl iodides under atmospheric pressure of carbon monoxide was achieved in the presence of a catalytic amount of MCM-41-supported bidentate phosphine palladium(0) complex [MCM-41-2P-Pd(0)] in good to high yields. This polymeric palladium catalyst can be reused at least 10 times without any decrease in activity.
Graphical abstractThe first heterogeneous carbonylative Sonogashira coupling reaction of terminal alkynes with aryl iodides under atmospheric pressure of CO was achieved in the presence of a catalytic amount of MCM-41-supported bidentate phosphine palladium(0) complex. This polymeric palladium catalyst can be reused at least 10 times without any decrease in activity.Figure optionsDownload full-size imageDownload as PowerPoint slide
