126800-27-9Relevant academic research and scientific papers
Photoredox Catalysis at Copper(II) on Chitosan: Application to Photolatent CuAAC
Jennah, Oumayma,Beniazza, Redouane,Lozach, Cédric,Jardel, Damien,Molton, Florian,Duboc, Carole,Buffeteau, Thierry,El Kadib, Abdelkrim,Lastécouères, Dominique,Lahcini, Mohammed,Vincent, Jean-Marc
, p. 4615 - 4624 (2018/10/26)
In this article we report the first example of a heterogeneous photolatent catalyst for the copper-catalyzed azide-alkyne cycloaddition (CuAAC) that is supported on chitosan. The heterogeneous copper(II) precatalyst was easily prepared by reaction of [Cu
The efficient copper(I) (hexabenzyl)tren catalyst and dendritic analogues for green "click" reactions between azides and alkynes in organic solvent and in water: Positive dendritic effects and monometallic mechanism
Liang, Liyuan,Ruiz, Jaime,Astruc, Didier
experimental part, p. 3434 - 3450 (2012/02/05)
An easily synthesized, copper(I) (hexabenzyl)tren complex 1 is an efficient catalyst for the copper(I)-catalyzed Huisgen-type 1,3-cycloaddition between azides and alkynes (CuAAC) reaction in toluene. Alternatively, a convenient procedure involves mixing c
A highly active and reusable copper(I)-tren catalyst for the "click" 1,3-dipolar cycloaddition of azides and alkynes
Candelon, Nicolas,Lastecoueres, Dominique,Diallo, Abdou Khadri,Ruiz Aranzaes, Jaime,Astruc, Didier,Vincent, Jean-Marc
, p. 741 - 743 (2008/09/17)
The copper(I) complex [Cu(C186tren)]Br 1 (C186tren = tris(2-dioctadecylaminoethyl)amine) which exhibits a good stability towards aerobic conditions is a versatile, highly reactive and recyclable catalyst for the Huisgen cycloaddition
Dipolar Cycloaddition Reactions of Organic Azides with some Acetylenic Compounds
Abu-Orabi, Sultan T.,Atfah, M. Adnan,Jibril, Ibrahim,Mari'i, Fakhri M.,Ali, Amer Al-Sheikh
, p. 1461 - 1468 (2007/10/02)
Phenyl azide 1 and several substituted benzyl azides 2a-o underwent 1,3-dipolar cycloaddition reactions with dimethyl acrtylenedicarboxylate 3, phenylacetylene 4 and ethyl propiolate 5 to afford the triazoles 6-13.The reactions of these azides with ethyl
