Dianions derived from chiral imidazolines la-c, undergo selective one-electron oxidation reactions in the presence of TEMPO (2,2,6, and form metallated radical species. Depending on the reaction conditions the radical intermediate is trapped stereoselectively by TEMPO, or undergoes a dimerization re
Stereoselective Triplet-Sensitised Radical Reactions of Furanone Derivatives
✍ Scribed by Rabih Jahjah; Abdoulaye Gassama; Véronique Bulach; Chikako Suzuki; Manabu Abe; Norbert Hoffmann; Agathe Martinez; Jean-Marc Nuzillard
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 583 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0947-6539
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