Click Reaction of Calcium Carbide-Derived Acetylene as a Direct Way to Chromophore- and Fluorophore-Substituted 1,2,3-Triazoles

被引:0
|
作者
Voronin, V. V. [1 ]
Ledovskaya, M. S. [1 ]
机构
[1] St Petersburg State Univ, Inst Chem, St Petersburg 199034, Russia
基金
俄罗斯科学基金会;
关键词
acetylene; click chemistry; CuAAC reaction; organic dyes; 1,2,3-triazoles; ONE-POT SYNTHESIS; ORGANIC-DYES; TRIAZOLES; PYRAZOLES; CELLS; CUAAC;
D O I
10.1134/S107036322412003X
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Abstract1-[4-(Phenyldiazenyl)phenyl]-1H-1,2,3-triazole and 3-(1H-1,2,3-triazol-1-yl)-2H-chromen-2-one were synthesized for the first time by using the copper-catalyzed azide-alkyne cycloaddition reaction of azobenzene- and coumarin-substituted azides and calcium carbide-derived acetylene. Both azobenzene- and coumarin-substituted substrates afforded target 1,2,3-triazoles in good yields by reacting with acetylene generated from calcium carbide and water directly in the reaction vessel. This work demonstrates the enhanced applicability of the calcium carbide approach in organic synthesis, including the synthesis of chromophore- and fluorophore-substituted compounds.
引用
收藏
页码:3149 / 3154
页数:6
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