Abstract
LTA reaction of homoallyl alcohols derived from norbornyl α-diketones exclusively furnished the corresponding α-diketones via β-fragmentation of the allyl group in refluxing benzene while changing the solvent to MeOH resulted in the formation of novel methoxy substituted spirocyclic tetrahydrofuran products.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 4239-4241 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Issue number | 41 |
| DOIs | |
| State | Published - Jan 1 2007 |