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Please use this identifier to cite or link to this item:
http://hdl.handle.net/10174/20889
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Title: | An “Out-of-the-Box” Example for Heterocyclic Chemistry: Synthesis of 3,6-Bis-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazine |
Authors: | Mendes, Paulo J. Silva, Tiago JL Tomaz, Ana Isabel Garcia, M. Helena |
Editors: | Afonso, Carlos A M Candeias, Nuno R Simão, Dulce Pereira Trindade, Alexandre F Coelho, Jaime A S Tan, Bin Franzen, Robert |
Keywords: | Heterocyclic ring formation Tetrazines |
Issue Date: | 2017 |
Publisher: | Royal Society of Chemistry |
Citation: | An “Out-of-the-Box” Example for Heterocyclic Chemistry: Synthesis of 3,6-Bis-(3,5-dimethyl-1H-pyrazol-1-yl)-1,2,4,5-tetrazine, T.J.L. Silva, P.J. Mendes, A.I. Tomaz & M.H. Garcia em Comprehensive Organic Chemistry Experiments for the Laboratory Classroom, C.A.M. Afonso, N.R. Candeias, D. Pereira Simão, A.F. Trindade, J.A.S. Coelho, B. Tan & R. Franzén (Eds.), RSC Publications, Cambridge, 2017, Cap.12.2.5, pp.745-749 (ISBN 978-1-84973-963-4) |
Abstract: | 3,6-Dissubsituted tetrazines
can be included in functional molecular systems for the development of sensors and optical
switches, electroactive polymers or solar cells. Tetrazine derivatives, namely dipyridyl-s-tetra-
zines and related molecules, have also been frequently used as bridging ligands in metallo-organic compounds. Their N-hydro (di, tetra, hexa) derivatives exhibit biological activity and some
have been tested for their anti-tumour activity. This experiment describes a simple procedure for the synthesis of 3,6-bis(3,5-dimethyl-1H-
pyrazol-1-yl)-s-tetrazine in moderate yield with a straightforward work-up. |
URI: | http://pubs.rsc.org/en/content/ebook/978-1-84973-963-4#!divbookcontent http://hdl.handle.net/10174/20889 |
ISBN: | 978-1-84973-963-4 |
Type: | bookPart |
Appears in Collections: | QUI - Publicações - Capítulos de Livros CQE - Publicações - Capítulos de Livros
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