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Updated: May 3, 2026

Regioselective O-Glycosylation of Nucleosides via the Temporary 2',3'-Diol Protection by a Boronic Ester for the Synthesis of Disaccharide Nucleosides
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Regioselective O-Glycosylation of Nucleosides via the Temporary 2',3'-Diol Protection by a Boronic Ester for the Synthesis of Disaccharide Nucleosides

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Protecting-group-free O-glysosidation using p-toluenesulfonohydrazide and glycosyl chloride donors

Rohan J Williams1, Caroline E Paul1, Mark Nitz1

  • 1Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada.

Carbohydrate Research
|February 5, 2014
PubMed

Keywords:
Glycosyl chloridesN′-GlycosylsulfonohydrazidesProtecting-group-free glycosidationProtecting-group-free glycosylation

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