1037412-73-9Relevant articles and documents
Solvent-free Suzuki and Stille cross-coupling reactions of 4- and 5-halo-1,2,3-triazoles
Gribanov, Pavel S.,Chesnokov, Gleb A.,Dzhevakov, Pavel B.,Kirilenko, Nikita Yu.,Rzhevskiy, Sergey A.,Ageshina, Alexandra A.,Topchiy, Maxim A.,Bermeshev, Maxim V.,Asachenko, Andrey F.,Nechaev, Mikhail S.
, p. 147 - 149 (2019)
An environmentally friendly and efficient synthesis of fully substituted 1,2,3-triazoles comprises solvent-free palladium-catalyzed Suzuki cross-coupling of halo-1,2,3-triazoles with pinacol arylboronates. The efficiencies of Stille and Suzuki reactions w
Copper(I) and palladium nanoparticles supported on ethylenediamine- functionalized cellulose as an efficient catalyst for the 1,3-dipolar cycloaddition/direct arylation sequence
Keshipour, Sajjad,Shaabani, Ahmad
, p. 116 - 119 (2014/02/14)
Cu(I) and nanoparticles of Pd supported on ethylenediamine-functionalized cellulose as a novel bio-supported catalyst was synthesized and characterized. The synthesized catalyst was found to be a highly efficient heterogeneous catalyst for the synthesis o
Copper-catalyzed "click" reaction/direct arylation sequence: Modular syntheses of 1,2,3-triazoles
Ackermann, Lutz,Potukuchi, Harish K.,Landsberg, Dirk,Vicente, Ruben
supporting information; experimental part, p. 3081 - 3084 (2009/05/07)
(Chemical Equation Presented) Inexpensive copper catalysts enabled modular one-pot multicomponent syntheses of fully decorated triazoles through a sustainable "click" reaction/direct arylation sequence.