1202246-86-3Relevant academic research and scientific papers
A layered double hydroxide, a synthetically useful heterogeneous catalyst for azide?alkyne cycloadditions in a continuous-flow reactor
ádok-Sipiczki, Mónika,?tv?s, Sándor B.,Fül?p, Ferenc,Georgiádes, ádám,Mészáros, Rebeka,Pálinkó, István,Sipos, Pál
, p. 63 - 73 (2020/12/04)
A Cu(II)Fe(III)-layered double hydroxide is shown to efficiently catalyze 1,3-dipolar cycloadditions of organic azides to alkynes leading to valuable 1,2,3-triazoles. The benefits of continuous processing were exploited for reaction optimization and synth
Continuous-flow azide-alkyne cycloadditions with an effective bimetallic catalyst and a simple scavenger system
?tv?s, Sndor B.,Hatoss, Gbor,Georgides, dm,Kovcs, Szabolcs,Mndity, Istvn M.,Novk, Zoltn,Fül?p, Ferenc
, p. 46666 - 46674 (2014/12/10)
A flow chemistry-based technique is presented herein for Cu(i)-catalyzed azide-alkyne cycloadditions with a copper on iron bimetallic system as the catalyst and iron powder as a readily available copper scavenger. The method proved to be rapid and safe as
Copper on iron: Catalyst and scavenger for azide-alkyne cycloaddition
Kovács, Szabolcs,Zih-Perényi, Katalin,Révész, ádám,Novák, Zoltán
supporting information, p. 3722 - 3730 (2013/02/22)
Dipolar cycloaddition of terminal alkynes and azides catalyzed by the Cu/Fe bimetallic system is reported. In the presence of a readily accessible nanosized copper source, the cycloaddition reaction can be easily achieved at ambient temperature with high
Highly active copper-catalysts for azide-alkyne cycloaddition
Gonda, Zsombor,Novak, Zoltan
supporting information; experimental part, p. 726 - 729 (2010/04/25)
Bis-triphenylphosphano complexes of copper(i)-carboxylates serve as efficient catalysts for azide-alkyne cycloaddition. The triazole formation takes place straightforwardly at ambient temperature providing a wide variety of products with good yields in th
The sequential Sonogashira-click reaction: A versatile route to 4-aryl-1,2,3-triazoles
Loerincz, Krisztian,Kele, Peter,Novak, Zoltan
experimental part, p. 3527 - 3532 (2010/02/28)
Aryl halides can be easily transformed in a one-pot procedure into 4-aryl-1,2,3-triazoles with palladium/copper-catalyzed Sonogashira-click reaction sequence, using trimethylsilylacetylene as acetylene surrogate.
