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Unsupported Copper Nanoparticles in the 1,3-Dipolar Cycloaddition of Terminal Alkynes and Azides
(Wiley VCH Verlag, 2010-04)
Readily prepared copper nanoparticles were found to catalyse the 1,3-dipolar cycloaddition of azides and alkynes up to rates comparable to those of microwave chemistry. Both the preparation of the nanoparticles and the ...
Copper nanoparticles in click chemistry: an alternative catalytic system for the cycloaddition of terminal alkynes and azides
(Pergamon-Elsevier Science Ltd, 2009-03)
Readily prepared copper nanoparticles have been found to effectively catalyse the 1,3-dipolar cycloaddition of a variety of azides and alkynes furnishing the corresponding 1,2,3-triazoles in excellent yields. Both the ...
Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) `click chemistry` in carbohydrate drug and neoglycopolymer synthesis
(PERGAMON-ELSEVIER SCIENCE LTD, 2010)
Cu2O spheres as an efficient source of catalytic Cu(I) species for performing azide-alkyne click reactions
(Tetrahedron Letters, 2018)
A straightforward and sustainable synthesis of 1,4-disubstituted 1,2,3-triazoles: Via visible-light-promoted copper-catalyzed azide-alkyne cycloaddition (CuAAC)
(Royal Society of Chemistry, 2017-06)
A simple and green synthesis of 1,4-disubstituted 1,2,3-triazoles through the effective reduction of copper(ii) assisted by organic dyes and promoted by visible light was developed. This reaction was performed under very ...
Cationic 1,2,3 triazolium alkynes : components to enhance 1,4 regioselective azide rlkyne cycloaddition reactions
(Universidad Autónoma Metropolitana. Unidad Lerma, 2016)
Copper-catalysed multicomponent click synthesis of 5-alkynyl 1,2,3-triazoles under ambient conditions
(Georg Thieme Verlag Kg, 2012-06)
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully substituted 5-alkynyl 1,2,3-triazoles from organic halides, sodium azide, and terminal alkynes in methanol under ambient ...
Synthesis of 5-Organotellanyl-1H-1,2,3-triazoles: Functionalization of the 5-Position Scaffold by the Sonogashira Cross-Coupling Reaction
(Wiley-v C H Verlag GmbhWeinheimAlemanha, 2013)