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.
Original language | English |
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Pages (from-to) | 7179-7183 |
Number of pages | 5 |
Journal | Tetrahedron Letters |
Volume | 47 |
Issue number | 40 |
DOIs | |
State | Published - 2 Oct 2006 |
Keywords
- Adamantane isoxazolines
- Enaminoketones
- Isomerization
- Photorearrangement