Related Experiment Video

Updated: Aug 19, 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

Synthesis and antitumoral evaluation of 3',4'-unsaturated nucleoside analogues bearing a chlorinated remdesivir-like

Song Wang1, Jing Yang2, Xinyue Yang1

  • 1XNA platform, School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan 450001, China.

Bioorganic Chemistry
|August 17, 2026
PubMed

Keywords:
3′,4′-unsaturated ribonucleosidesAnti-HepG2Chlorinated remdesivir-like baseKinase-associated mechanism

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