93691-36-2Relevant academic research and scientific papers
Arylazide cycloaddition to methyl propiolate: DFT-based quantitative prediction of regioselectivity
Molteni, Giorgio,Ponti, Alessandro
, p. 2770 - 2774 (2003)
Several 1-(4-substituted)-phenyl-4- or 5-methoxycarbonyl-1,2,3-triazoles have been synthesized by 1,3-dipolar cycloaddition of the corresponding arylazides to methyl propiolate in carbon tetrachloride. The regioselectivity of these reactions cannot be rat
Silver(I) oxide nanoparticles as a catalyst in the azide-alkyne cycloaddition
Ferretti, Anna M.,Ponti, Alessandro,Molteni, Giorgio
supporting information, p. 5727 - 5730 (2015/09/29)
1,3-Dipolar cycloadditions between a number of azides and monosubstituted acetylenes have been carried out in the presence of catalytic amounts of silver(I) oxide nanoparticles. 4-Substituted 1,2,3-triazoles were usually the only products, while the prese
