Related Experiment Video

Updated: Sep 4, 2026

Regioselective O-Glycosylation of Nucleosides via the Temporary 2',3'-Diol Protection by a Boronic Ester for the Synthesis of Disaccharide Nucleosides
08:46

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

Published on: July 26, 2018

Conformationally constrained glycosyl fluoride donors enable chemoselective glycosylation

Timothy M Emmel1, Joshua L Martin1, John Montgomery1

  • 1Department of Chemistry, University of Michigan 930 N. University Ave. Ann Arbor MI 48109-1055 USA jmontg@umich.edu.

Organic Chemistry Frontiers : an International Journal of Organic Chemistry
|September 3, 2026
PubMed

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