‘Click’ ligand for ‘click’ chemistry: (1-(4-methoxybenzyl)-1-H-1,2,3-triazol-4-yl)methanol (MBHTM) accelerated copper-catalyzed [3+2] azide–alkyne cycloaddition (CuAAC) at low catalyst loading
Authors:
- 1 October 2015
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 56 (43) , 5864-5869
Abstract
No abstract availableKeywords
Funding Information
- DST (SR/FT/CS-85/2011)
This publication has 33 references indexed in Scilit:
- Click Chemistry in Materials ScienceAdvanced Functional Materials, 2014
- Click Chemistry Inspired Synthesis of Glycoporphyrin DendrimersThe Journal of Organic Chemistry, 2013
- Europium confined cyclen dendrimers with photophysically active triazolesJournal of Materials Chemistry, 2008
- The growing applications of click chemistryChemical Society Reviews, 2007
- In situclick chemistry: a powerful means for lead discoveryExpert Opinion on Drug Discovery, 2006
- Multivalent, bifunctional dendrimers prepared by click chemistryChemical Communications, 2005
- The growing impact of click chemistry on drug discoveryDrug Discovery Today, 2003
- Azide–Alkyne Coupling: A Powerful Reaction for Bioconjugate ChemistryChemBioChem, 2003
- A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal AlkynesAngewandte Chemie International Edition, 2002
- Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to AzidesThe Journal of Organic Chemistry, 2002