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) |
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Pages (from-to) | 4239-4241 |
Number of pages | 3 |
Journal | Chemical Communications |
Issue number | 41 |
DOIs | |
State | Published - Jan 1 2007 |