Aziridination of α,β-unsaturated ketones
✍ Scribed by Stefania Fioravanti; Lucio Pellacani; Stefania Tabanella; Paolo A. Tardella
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 411 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
Akstra~. ~l~-Unsaturated ketones are aziridinated by [(arenesulphonyl)oxy]carbamates and CaO (or Cs2CO3) or by N3CO2Et photolysis. A remote chiral center induced up m 74% ~e. Bis-unsaturated subeuates showed scarce regioselectivity under all conditions.
📜 SIMILAR VOLUMES
Synthetic precursors of amino phosphonic acids are aziridinyl phosphonates. These compounds can be prepared through a reaction of phosphonates 2a-e with NsONHCO 2 Et and inorganic bases involving addition of an (ethoxycarbonyl)amino group onto the double bond, via a new and easy procedure.
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