ChemInform Abstract: First Synthesis of Anomeric Sulfimides — Efficient Glycosyl Donors.
✍ Scribed by S. CASSEL; I. PLESSIS; H. P. WESSEL; P. ROLLIN
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
First Synthesis of Anomeric Sulfimides -Efficient Glycosyl Donors.
-Carbohydrate-derived sulfimides of type (III) are efficiently prepared by reaction of the corresponding thioglycosides with chloramine T. They are investigated as glycosyl donors with a variety of alcohols. In several cases the anomeric ratio of the resulting glycosides [cf. (V), (VII), and (VIII)] is found to be highly dependent on the nature of the solvent. -(CASSEL, S.
📜 SIMILAR VOLUMES
We introduce a convenient synthesis of anomeric sulfimides, the ability of which to act as glycosyl donors has been tested with various thiophilic reagents and acceptors.