Aziridine Ring Opening as Regio- and Stereoselective Access to C-Glycosyl-Aminoethyl Sulfide Derivatives
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DOI: 10.3390/molecules27061764
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.… read more here.
Keywords: glycosyl aminoethyl; ring opening; access glycosyl; sulfide derivatives ... See more keywords