Short synthesis, X-ray and conformational analysis of a cyclic peracetylated L-sorbose-derived nitrone, a useful intermediate towards N–O-containing D-gluco-iminosugars
A crystalline peracetylated nitrone underwent regio- and stereoselective 1,3-dipolar cycloaddition with alkynes, affording gluco-configured isoxazolines as a new class of iminosugars.
Références
- Titre
- Short synthesis, X-ray and conformational analysis of a cyclic peracetylated L-sorbose-derived nitrone, a useful intermediate towards N–O-containing D-gluco-iminosugars
- Type de publication
- Article de revue
- Année de publication
- 2018
- Auteurs
- Tangara, Salia, Kanazawa Alice, Fayolle Martine, Philouze Christian, Poisson Jean-François, Behr Jean-Bernard, and Py Sandrine
- Revue
- New Journal of Chemistry
- Volume
- 42
- Pagination
- 16735–16743
- Date de publication
- 10/2018
- ISSN
- 1144-0546
Soumis le 18 octobre 2018