Abstract
A new method for the synthesis of 2,3-dihydrofurans from readily available starting enones and pyridinium salts has been developed. This protocol can provide a novel and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective fashion. To increase the efficiency of this reaction the one-pot process was also developed, in which the pyridinium salts were generated in situ from corresponding halides.
| Original language | English |
|---|---|
| Pages (from-to) | 675-679 |
| Number of pages | 5 |
| Journal | Synthesis |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2006 Feb 15 |
All Science Journal Classification (ASJC) codes
- Catalysis
- Organic Chemistry