Abstract
A tBu3P-coordinated 2-phenylaniline-based palladacycle complex was demonstrated to be an efficient precatalyst for Pd-catalyzed coupling reactions of aryl halides with polyfluoroarenes that operates through a C-H activation strategy. The ready accessibility and ease of handling of the complex and the high yields of the reaction makes this palladacycle complex an attractive precatalyst for the cross-coupling reaction of aryl halides with polyfluoroarenes. A tBu3P-coordinated 2-phenylaniline-based palladacycle complex was found to be an efficient precatalyst for Pd-catalyzed coupling reactions of aryl halides with polyfluoroarenes that operates through a C-H activation strategy, with good to excellent product yields being observed.
| Original language | English |
|---|---|
| Pages (from-to) | 1327-1332 |
| Number of pages | 6 |
| Journal | European Journal of Organic Chemistry |
| Volume | 2014 |
| Issue number | 6 |
| DOIs | |
| State | Published - Feb 2014 |
| Externally published | Yes |
Keywords
- C-C coupling
- C-H activation
- Fluorine
- Metallacycles
- Palladium
- Synthetic methods