| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1253954 | Chinese Chemical Letters | 2016 | 4 Pages |
A simple and highly efficient protocol has been developed for the Pd/C-catalyzed ligand-free Suzuki–Miyaura reaction of potassium aryltrifluoroborates. In this catalytic system, the results demonstrate that oxygen plays a positive role in the cross-coupling reaction. In addition, this catalytic system could be successfully applied to synthesize biaryl compounds containing a carbazole moiety and the catalyst was recycled seven times without significant loss of catalytic activity.
Graphical abstractAn efficient protocol has been developed for the Pd/C-catalyzed ligand-free Suzuki–Miyaura reaction of potassium aryltrifluoroborates. The results demonstrate that oxygen plays a positive role in the cross-coupling reaction. In addition, this catalytic system could be successfully applied to synthesize biaryl compounds containing a carbazole moiety and the catalyst was recycled seven times without significant loss of catalytic activity.Figure optionsDownload full-size imageDownload as PowerPoint slide
