This submission belongs to the session c. Microwave Assisted Synthesis of the event The 18th International Electronic Conference on Synthetic Organic Chemistry
Published date
03 Nov, 2014
Citation
Julio A. Seijas, Alberto Diaz-Seivane, María García-Fernández, M. Pilar Vázquez-Tato, Microwave Assisted Synthesis of Tripodal Tris(1H-1,2,3-triazol-4-yl) Cyanurates and Melamines, in Proceedings of The 18th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2014, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-18-c013
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Microwave Assisted Synthesis of Tripodal Tris(1H-1,2,3-triazol-4-yl) Cyanurates and Melamines
Julio A. Seijas 1
Alberto Diaz-Seivane 1
María García-Fernández 1
M. Pilar Vázquez-Tato 1
1. Departamento de Química Orgánica. Facultade de Ciencias. Universidade de Santiago de Compostela. Campus Terra. 27080-Lugo. Spain
Abstract
2,4,6-tris(prop-2-yn-1-yloxy)-1,3,5-triazine and N2,N4,N6-tri(prop-2-yn-1-yl)-1,3,5-triazine-2,4,6-triamine are used in click reactions to prepare tripodal compounds and dendrimer cores. So, 1,3-cycloaddition with benzyl azide under microwave irradiation afforded 2,4,6-tris((1-benzyl-1H-1,2,3-triazol-4-yl)methoxy)-1,3,5-triazine and N2,N4,N6-tris((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)-1,3,5-triazine-2,4,6-triamine, in a 1 minute reaction with good yields.
Keywords
Triazole
triazine
tripodal
dendrimer
microwave
Manuscript
jasvecsoc18pilarjasvfinal.pdf
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