| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278137 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
The Mo(CO)6-mediated photoinduced ring-opening reactions of adamantane isoxazolines involve novel rearrangement that provide enaminoketones as major products and β-hydroxy ketones as minor ones; in contrast, only β-hydroxy ketones and α,β-unsaturated ketones were obtained under thermal condition.
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