Abstract
Mo(CO)6-mediated ring opening reactions of calix[4]arene isoxazolines/isoxazoles provide a new synthetic methodology for calix[4]arenes carrying bifunctional β-hydroxy ketones or α,β-unsaturated-β-amino ketones. Mo(CO)6 is a highly selective and convenient reagent for the ring opening process of these supramolecular isoxazolines/isoxazoles.
| Original language | English |
|---|---|
| Pages (from-to) | 9077-9081 |
| Number of pages | 5 |
| Journal | Tetrahedron Letters |
| Volume | 47 |
| Issue number | 51 |
| DOIs | |
| State | Published - 18 Dec 2006 |
Keywords
- α,β-Unsaturated-β-amino ketones
- β-Hydroxy ketones
- Calix[4]arene isoxazolines/isoxazoles
- Molybdenum hexacarbonyl
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Senthilvelan, A., Tsai, M. T., Chang, K. C., & Chung, W-S. (2006). Mo(CO)6-mediated synthesis of calix[4]arenes carrying β-hydroxy ketones or α,β-unsaturated-β-amino ketones. Tetrahedron Letters, 47(51), 9077-9081. https://doi.org/10.1016/j.tetlet.2006.10.082