This submission belongs to the session a. General Organic Synthesis of the event The 15th International Electronic Conference on Synthetic Organic Chemistry
Published date
25 Oct, 2011
Citation
M. Pilar Vázquez-Tato, Xesús Feás, Marta Carracedo-Taboada, Julio A Seijas, Click reactions in the synthesis of tripodal 1H-1,2,3-triazol derivatives of 1,3,5-triazinane-2,4,6-trione, in Proceedings of The 15th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2011, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-15-00689
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Click reactions in the synthesis of tripodal 1H-1,2,3-triazol derivatives of 1,3,5-triazinane-2,4,6-trione
M. Pilar Vázquez-Tato 1
Xesús Feás 1
Marta Carracedo-Taboada 1
Julio A Seijas 1
1. Department of Organic Chemistry. Facultade de Ciencias. Universidade de Santiago de Compostela. Aptdo. 280. 27080-Lugo. Spain
Abstract
The copper catalyzed Huisgen reaction was used for the synthesis of two derivatives of 1H-1,2,3-triazol-1,3,5-triazinane-2,4,6-trione. One from tris(2-azidoethyl)-1,3,5-triazinane-2,4,6-trione and phenylacetylene, and the other by coupling of 1,3,5-tri(prop-2-yn-1-yl)-1,3,5-triazinane-2,4,6-trione with benzyl azide.
Keywords
Huisgen,1,3,5-triazinane-2,4,6-trione
C3-symmetry
Membrane permeation properties of benzo[a]phenoxazinium fluorescent probes using molecular modelling techniques
Synthesis of triols with C3 symmetry by ring opening of tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione with nucleophiles