Chemical Communications · 2015 · 121 citations · 51 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryCross-coupling ReactionsDiversity-oriented SynthesisHeterocycle SynthesisHeterocyclic ChemistryMetal CatalysisStrain-promoted CycloadditionAlkyne Cycloaddition ReactionsMetal CatalystsMetal-free CatalystsStrain-promoted Alkyne-azide CycloadditionStrain-promoted Azide - Alkyne CycloadditionTransition Metal CatalystsTriazole ChemistryTriazole Synthesis
Metal-free 1,3-dipolar cycloaddition reactions have proven to be a powerful tool for the assembly of key heterocycles, in particular diversely functionalized 1,2,3-triazoles. A number of metal-free (3+2)-cycloaddition approaches have been developed up to date with the aim to circumvent the use of metal catalysts allowing these reactions to take place in biological systems without perturbation of the naturally occurring processes. This feature article specifically provides an overview of emerging metal-free synthetic routes, and their mechanistic features, in the formation of functionalized 1,2,3-triazoles.
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In Vivo Imaging of Membrane-Associated Glycans in Developing Zebrafish
Scott T. Laughlin, Jeremy M. Baskin, Sharon L. Amacher et al. · Science · 2008 · 1K citations · Full text