Abstract
A useful and effective rhodium catalyst system - [RhCl(PPh 3)3/DPPF] - for the Suzuki-Miyaura cross-coupling of activated alkenyl tosylates is described. The results not only represent the first examples of the rhodium-catalyzed Suzuki-Miyaura coupling of activated alkenyl tosylates with arylboronic acids under mild conditions, but also provide an efficient route for the synthesis of some natural product-like compounds, such as furan-2(5H)-one, coumarin, pyrone, and quinolin-2(1H)-one derivatives.
| Original language | English |
|---|---|
| Pages (from-to) | 5260-5263 |
| Number of pages | 4 |
| Journal | European Journal of Organic Chemistry |
| Issue number | 23 |
| DOIs | |
| State | Published - 27 Nov 2006 |
| Externally published | Yes |
Keywords
- 1,1′-bis(diphenylphosphanyl)ferrocene
- Activated alkenyl tosylates
- Cross-coupling
- Natural product-like compounds
- Rhodium
Fingerprint
Dive into the research topics of 'RhCl(PPh3)3/DPPF: A useful and efficient catalyst for cross-coupling reactions of activated alkenyl tosylates with arylboronic acids'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver