Abstract
In this paper the synthesis of a library of new 1,4-disubstituted 1,2,3-triazoles 1, with a variety of additional functional groups on its structure, from an in situ generated benzyl azide 2 and different alkynes and dialkynes 3 is reported. Optimal experimental conditions were established for the conventional click chemistry and for the microwave-assisted synthesis of these 1,2,3-triazoles. Comparing the results it was concluded that under microwave-assisted conditions the products are obtained in higher yields in shorter times. © ARKAT-USA, Inc.
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CITATION STYLE
Sarmiento-Sánchez, J. I., Ochoa-Terán, A., & Rivero, I. A. (2011). Conventional and microwave assisted synthesis of 1,4-disubstituted 1,2,3-triazoles from Huisgen cycloaddition. Arkivoc, 2011(9), 177–188. https://doi.org/10.3998/ark.5550190.0012.913
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