Related Experiment Video

Updated: Sep 26, 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

Diversification of Nucleosides Via Radical Mediated Deoxygenative Functionalization

Maochao Zhou1, Gang He1,2

  • 1State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, China.

Current Protocols
|September 25, 2026
PubMed

Keywords:
2'‐O‐BDT‐adenosine3'‐O‐BDT‐thymidineC‐O bond activationbenzodithiolanemodified nucleosides

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