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- Title
Aziridine Ring Opening as Regio- and Stereoselective Access to C -Glycosyl-Aminoethyl Sulfide Derivatives.
- Authors
Tracz, Aleksandra; Malinowska, Martyna; Leśniak, Stanisław; Zawisza, Anna
- Abstract
A short synthetic route to stereoselective access to C-glycosyl-aminoethyl sulfide derivatives has been developed through the reaction of tributhyltin derivatives of glycals with aziridinecarboaldehyde and the regioselective ring opening of a chiral aziridine with thiophenol. The absolute configurations of the resulting diastereoisomers were determined by 1H NMR spectroscopy.
- Subjects
SULFIDES; NUCLEAR magnetic resonance spectroscopy; GLYCALS; DIASTEREOISOMERS
- Publication
Molecules, 2022, Vol 27, Issue 6, p1764
- ISSN
1420-3049
- Publication type
Article
- DOI
10.3390/molecules27061764