Micellar media in water provide a simple and efficient environment to favor the multi-component synthesis of 1,2,3-triazoles from organic bromides, sodium azide and terminal alkynes in the presence of [Cu(IMes)Cl] 1 catalyst at room temperature within few hours. The micellar medium favors both the in situ formation of the organic azide and its metal promoted cycloaddition with the alkyn
A new bistriazole copper complex was synthesized by direct treatment of an alkyne, an azide, and CuI...
Transition-metal-catalyzed or metal-free azide-alkyne cycloadditions are methods to access 1,4- or 1...
1H-1,2,3-triazoles can be prepared in good yield by the reaction of terminal alkyne and sodium azide...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Copper nanoparticles on activated carbon have been found to effectively catalyze the multicomponent ...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
1,4-disubstituted 1,2,3-triazoles are obtained in high yields via one-pot three components reaction ...
A variety of potentially biologically active 1,2,3-triazoles, derived from (–)-menthol, lactic acid,...
1,2,3-Triazoles, which can be readily prepared from click chemistry, are important building componen...
A new bistriazole copper complex was synthesized by direct treatment of an alkyne, an azide, and CuI...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
A new bistriazole copper complex was synthesized by direct treatment of an alkyne, an azide, and CuI...
Transition-metal-catalyzed or metal-free azide-alkyne cycloadditions are methods to access 1,4- or 1...
1H-1,2,3-triazoles can be prepared in good yield by the reaction of terminal alkyne and sodium azide...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
Copper nanoparticles on activated carbon have been found to effectively catalyze the multicomponent ...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
1,4-disubstituted 1,2,3-triazoles are obtained in high yields via one-pot three components reaction ...
A variety of potentially biologically active 1,2,3-triazoles, derived from (–)-menthol, lactic acid,...
1,2,3-Triazoles, which can be readily prepared from click chemistry, are important building componen...
A new bistriazole copper complex was synthesized by direct treatment of an alkyne, an azide, and CuI...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
A new bistriazole copper complex was synthesized by direct treatment of an alkyne, an azide, and CuI...
Transition-metal-catalyzed or metal-free azide-alkyne cycloadditions are methods to access 1,4- or 1...
1H-1,2,3-triazoles can be prepared in good yield by the reaction of terminal alkyne and sodium azide...