Authors | H Naeimi, S Dadashzadeh, M Moradian |
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Journal | RES CHEM INTERMEDIAT |
Page number | 2687 |
Volume number | 41 |
IF | 1.221 |
Paper Type | Full Paper |
Published At | 2015-06-11 |
Journal Grade | Scientific - research |
Journal Type | Electronic |
Journal Country | Iran, Islamic Republic Of |
Journal Index | ISI ,SCOPUS |
Abstract
A facile and highly efficient method for regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles in good to excellent yields from in-situ-generated azides and terminal alkynes by Cu(I)-catalyzed 1,3 dipolar cycloaddition (the so-called click reaction), is described. The reaction proceeds smoothly in a 1:1 mixture of water and ethanol at room temperature without any additive. The method is a convenient means of preparation of a wide range of triazoles in a one-pot operation via a three-component reaction.
tags: Synthesis 1,2,3-Triazole Ultrasound Catalyst Click chemistry 1,3-Dipolar cycloaddition