Abstract
1,2,3-triazoles were synthesized using several alkynes and azides as starting materials in the presence of catalytic amounts of Cu-Fe nanoparticles. The process represents many advantages because it does not require additional bases or reductants, and this is carried out under ambient pressure and temperature with good yields.
Keywords: 1,2,3-triazoles, alkynes, azides, nanoparticles, CuAAC, phenylacetylene, cycloaddition, bromide, sodium, aqueous mixture
Letters in Organic Chemistry
Title: Alkyne-Azide Cycloaddition Catalyzed by Fe-Cu Nanoparticles
Volume: 9 Issue: 3
Author(s): Angel Garcia-Munoz, Jaime Gonzalez, Jessica Trujillo-Reyes, Raul A. Morales-Luckie, Victor Sanchez-Mendieta, Carlos Gonzalez, Aydee Fuentes and Erick Cuevas-Yanez
Affiliation:
Keywords: 1,2,3-triazoles, alkynes, azides, nanoparticles, CuAAC, phenylacetylene, cycloaddition, bromide, sodium, aqueous mixture
Abstract: 1,2,3-triazoles were synthesized using several alkynes and azides as starting materials in the presence of catalytic amounts of Cu-Fe nanoparticles. The process represents many advantages because it does not require additional bases or reductants, and this is carried out under ambient pressure and temperature with good yields.
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Cite this article as:
Garcia-Munoz Angel, Gonzalez Jaime, Trujillo-Reyes Jessica, A. Morales-Luckie Raul, Sanchez-Mendieta Victor, Gonzalez Carlos, Fuentes Aydee and Cuevas-Yanez Erick, Alkyne-Azide Cycloaddition Catalyzed by Fe-Cu Nanoparticles, Letters in Organic Chemistry 2012; 9 (3) . https://dx.doi.org/10.2174/157017812800167457
DOI https://dx.doi.org/10.2174/157017812800167457 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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