Related Experiment Video

Updated: Sep 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

Electrochemical glycosylation using o-[1-(p-MeO-phenyl)vinyl]benzoates (PMPVB) as glycosylation donors

Mahendra K V Rotta1, Rajesh Lenka1, Sangay Moktan1

  • 1CHEL-301, Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India. pavankancharla@iitg.ac.in.

Chemical Communications (Cambridge, England)
|September 17, 2026
PubMed

More Related Videos

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis09:56

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis

Published on: September 6, 2019

Bridging the Bio-Electronic Interface with Biofabrication16:38

Bridging the Bio-Electronic Interface with Biofabrication

Published on: June 6, 2012

Related Concept Videos

Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation01:22

Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation

Baeyer–Villiger oxidation converts aldehydes to carboxylic acids and ketones to esters. The reaction uses peroxy acids or peracids and is often catalyzed by acid. The reaction is named after its pioneers, Adolf von Baeyer and Victor Villiger. The reaction is achieved by a wide range of peracids such as m-chloroperoxybenzoic acid (mCPBA), perbenzoic acid (C6H5COOOH), peracetic acid (CH3COOOH), hydrogen peroxide (H2O2), and tert-butyl hydroperoxide (t-BuOOH).
The carbonyl center is activated by...