Abstract
A combination of Pd(OAc)2 (5 mol %), PPh3 (10 mol %), and Et3B (200 mol %) promotes the formation of allyl phenyl sulfones from the allylic alcohols directly with excellent yields under mild conditions. The activation of an alcohol group is not necessary which is achieved in situ. The conjugated dienols also were equally effective for the said transformation.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 6506-6507 |
| Number of pages | 2 |
| Journal | Journal of Organic Chemistry |
| Volume | 70 |
| Issue number | 16 |
| DOIs | |
| State | Published - Aug 5 2005 |
| Externally published | Yes |
Fingerprint
Dive into the research topics of 'Palladium-triethylborane-triggered direct and regioselective conversion of allylic alcohols to allyl phenyl sulfones?'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS