104926-75-2Relevant academic research and scientific papers
Multi-component reaction for the preparation of 1,5-disubstituted 1,2,3-triazoles by in-situ generation of azides and nickel-catalyzed azide-alkyne cycloaddition
Camberlein, Virgyl,Kraupner, Nicolas,Bou Karroum, Nour,Lipka, Emmanuelle,Deprez-Poulain, Rebecca,Deprez, Benoit,Bosc, Damien
, (2021)
An efficient one-pot procedure combining bromide conversion into azide followed by NiAAC for the preparation of 1,5-disubstituted 1,2,3-triazoles has been developed. This procedure prevents the use of isolated azides, which are insufficiently commercially
A tunable route to oxidative and eliminative [3+2] cycloadditions of organic azides with nitroolefins: CuO nanoparticles catalyzed synthesis of 1,2,3-triazoles under solvent-free condition
Gangaprasad,Paul Raj,Kiranmye,Sasikala,Karthikeyan,Kutti Rani,Elangovan
supporting information, p. 3105 - 3108 (2016/07/06)
A regioselective and tunable synthesis of 1,5-disubstituted 1,2,3-triazloles from oxidative and eliminative [3+2] cycloadditions of nitroolefins and organic azides under solvent-free condition in the presence and absence of commercially available CuO nano
