## Abstract magnified image Asymmetric 1,3‐dipolar cycloadditions of chiral nitrones to 1‐propene‐1,3‐sultone (**1**) were investigated. Chiral nitrones **6a‐e** reacted with sultone **1** in toluene at 90 °C for 24‐36 h to give the corresponding isoxazolidines in moderate yields with high regiose
Stereoselective 1,3-dipolar cycloadditions of nitrones derived from amino acids. Asymmetric synthesis of N-(alkoxycarbonylmethyl)-3-hydroxypyrrolidin-2-ones
✍ Scribed by Merino, Pedro; Greco, Graziella; Tejero, Tomás; Hurtado-Guerrero, Ramon; Matute, Rosa; Chiacchio, Ugo; Corsaro, Antonino; Pistarà, Venerando; Romeo, Roberto
- Book ID
- 121080948
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- French
- Weight
- 436 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0040-4020
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