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New copper-containing catalysts based on modified amorphous silica and their use in flow azide—alkyne cycloaddition
synthesized in the flow regime showed higher activity in the catalytic cycloaddition of azides to alkynes than

Azide pre-click modification of chitosan: N-(2-azidoethyl)chitosan of the reduction product with sodium azide. The course of the formation of the Schiffbase (this step is determining

Click reactions in chitosan chemistry and biological properties. The reactions of copper-catalyzed azide—alkyne cycloaddition and the click reactions

Synthesis of new p-tert-butylcalix[4]arene derivatives containing photopolymerizable 1,3-butadiyne fragments. The functionalization can be readily accomplished via copper-catalyzed azide–alkyne cycloaddition under mild conditions.

Bifunctional derivatives of (Thia)calix[4]arenes with terminal double and triple bonds: Synthesis and azide-alkyne click reactions cycloaddition reactions with azides. © ISUCT Publishing.

Novel cyano-activated Cu(ii) complexes of arylhydrazones of active methylene nitriles and their catalytic application for azide-alkyne cycloaddition in water and glycerol was investigated for the microwave assisted 1,3-dipolar azide-alkyne cycloaddition reaction using a mixture

Mechanistic study in azide-alkyne cycloaddition (CuAAC) catalyzed by bifunctional trinuclear copper(I) pyrazolate complex: Shift in rate-determining stepTrinuclear copper(I) pyrazolate [Cu(3,5-(CF3)2Pz)]3 was employed in a mechanistic study of azide-alkyne

Novel cyano-activated Cu(ii) complexes of arylhydrazones of active methylene nitriles and their catalytic application for azide–alkyne cycloaddition in water and glycerol and their catalytic application for azide–alkyne cycloaddition in water and glycerol

Eight-membered-ring diaminocarbenes bearing naphthalene moiety in the backbone: DFT studies, synthesis of amidinium salts, generation of free carbene, metal complexes, and solvent-free copper catalyzed azide-alkyne cycloaddition (CuAAC) reaction in alkyne-azide cycloaddition (CuAAC) reaction under solvent-free conditions. © The Royal Society

Recent advances in the synthesis of bioactive quinoline-based 1,2,3-triazoles via cu-catalyzed huisgen 1,3-dipolar cycloaddition (“click reaction”) copper-catalyzed azide-alkyne cycloaddition methodology. Objective: The aim of the present review

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