| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5225834 | Tetrahedron | 2010 | 6 Pages |
Abstract
A perbenzylated 3,3-difluorinated hexono-1,5-lactone was prepared in several steps. Reaction of this lactone with MeOH/p-TsOH followed by a treatment with ion-exchange resin led to the formation of an exocyclic oxetane derived vinylether. Similar reaction with ammonia gave the corresponding carboxamido substituted oxetane in good yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
René Csuk, Erik Prell,