1361946-54-4Relevant academic research and scientific papers
Multicomponent azide-alkyne cycloaddition catalyzed by impregnated bimetallic nickel and copper on magnetite
Perez, Juana M.,Cano, Rafael,Ramon, Diego J.
, p. 23943 - 23951 (2014/06/24)
A new bimetallic catalyst derived from nickel and copper has been used successfully for the first time in the multicomponent reaction of terminal alkynes, sodium azide, and benzyl bromide derivatives. The presence of both metallic species on the surface of magnetite seems to have a positive and synergetic effect. The catalyst loading is the lowest ever published for a catalyst of copper anchored on any type of iron support. The catalyst could be easily removed from the reaction media just by magnetic decantation and it could be reused up to ten times without any negative effect on the initial results. The Royal Society of Chemistry 2014.
The first well-defined silver(I)-complex-catalyzed cycloaddition of azides onto terminal alkynes at room temperature
McNulty, James,Keskar, Kunal,Vemula, Ramesh
supporting information; experimental part, p. 14727 - 14730 (2012/01/19)
Silver(I)-catalyzed click chemistry: Substituted 1,2,3-triazoles are versatile intermediates with an expanding array of applications. The discovery and application of a general AgI-catalyzed azide-alkyne cycloaddition reaction (AAC) leading to
