Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully substituted 5-alkynyl 1,2,3-triazoles from organic halides, sodium azide, and terminal alkynes in methanol under ambient conditions.This work was generously supported by the Spanish Ministerio de Ciencia e Innovación (MICINN; CTQ2007-65218 and Consolider Ingenio 2010-CSD2007-00006), the Generalitat Valenciana (GV; PROMETEO/2009/039), and Fondo Europeo de Desarrollo Regional (FEDER). Y. M. acknowledges the Instituto de Síntesis Orgánica (ISO) of the Universidad de Alicante for a grant
1,4-Disubstituted-1,2,3-triazoles, considered as an important and useful class of heterocycles with ...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
1,4-disubstituted 1,2,3-triazoles are obtained in high yields via one-pot three components reaction ...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
A copper(I)-catalyzed tandem CuAAC/alkynylation reaction of various alkynes, organic azides, and br...
Copper nanoparticles on activated carbon have been found to effectively catalyze the multicomponent ...
A variety of potentially biologically active 1,2,3-triazoles, derived from (–)-menthol, lactic acid,...
Readily prepared copper nanoparticles were found to catalyse the 1,3-dipolar cycloaddition of azides...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
A one-pot protocol for the synthesis of 1,2,3-triazoles has been developed starting from inactivated...
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...
An easy-to-prepare, reusable and versatile catalyst consisting of oxidised copper nanoparticles on a...
1,4-Disubstituted-1,2,3-triazoles, considered as an important and useful class of heterocycles with ...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
1,4-disubstituted 1,2,3-triazoles are obtained in high yields via one-pot three components reaction ...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
Copper(I) oxide has been found to effectively catalyse the multicomponent click synthesis of fully s...
A copper(I)-catalyzed tandem CuAAC/alkynylation reaction of various alkynes, organic azides, and br...
Copper nanoparticles on activated carbon have been found to effectively catalyze the multicomponent ...
A variety of potentially biologically active 1,2,3-triazoles, derived from (–)-menthol, lactic acid,...
Readily prepared copper nanoparticles were found to catalyse the 1,3-dipolar cycloaddition of azides...
Micellar media in water provide a simple and efficient environment to favor the multi-component synt...
A one-pot protocol for the synthesis of 1,2,3-triazoles has been developed starting from inactivated...
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...
An easy-to-prepare, reusable and versatile catalyst consisting of oxidised copper nanoparticles on a...
1,4-Disubstituted-1,2,3-triazoles, considered as an important and useful class of heterocycles with ...
Copper(II) carboxylates are reduced efficiently by methanol in the presence of alkynes and form yell...
1,4-disubstituted 1,2,3-triazoles are obtained in high yields via one-pot three components reaction ...