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New 1,3,4-Oxadiazolyl-pyrazolyl-Pyridine Tricyclic Scaffold Derivatives: Synthesis and Structure Assignment by NMR and DFT Calculations
New 1,3,4-Oxadiazolyl-pyrazolyl-Pyridine Tricyclic Scaffold Derivatives: Synthesis and Structure Assignment by NMR and DFT Calculations
Paim, Gisele R.; Meira, Susiane C.; Pittaluga, Everton P.; Porte, Liliane M. F.; Meyer, Alexandre R.; Navarini, Jussara; Bonacorso, Helio G.
Abstract:
Among five-membered aromatic heterocycles, 1,3,4- oxadiazoles are important class of aromatic heterocycles displaying a broad spectrum of biological activities, such as antimicrobial, anti-inflammatoy, analgesic, anticonvulsivant, anti-hypoglycemic. Compounds containing oxadiazole moieties have been described as possessing anticancer or muscle relaxant activity and have been used as fluorescent whiteners. Usually, the synthesis of non-symmetrical 2,5-disubstituted 1,3,4- oxadiazoles has mainly been done by dehydratation of diacylhydrazines or oxidative cyclization of aldehyde N-acylhydrazones, but many other reagents and reaction conditions have been reported to achieve their obtainment.
Among five-membered aromatic heterocycles, 1,3,4- oxadiazoles are important class of aromatic heterocycles displaying a broad spectrum of biological activities, such as antimicrobial, anti-inflammatoy, analgesic, anticonvulsivant, anti-hypoglycemic. Compounds containing oxadiazole moieties have been described as possessing anticancer or muscle relaxant activity and have been used as fluorescent whiteners. Usually, the synthesis of non-symmetrical 2,5-disubstituted 1,3,4- oxadiazoles has mainly been done by dehydratation of diacylhydrazines or oxidative cyclization of aldehyde N-acylhydrazones, but many other reagents and reaction conditions have been reported to achieve their obtainment.
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DOI: 10.5151/chempro-15bmos-BMOS2013_2013610185416
Referências bibliográficas
- [1] 1 (a) Gaonkar, S. L.; Rai,. K. M. L.; Prabhuswamy, B. Eur J Med Chem
- [2] 2006, 41, 841. (b) Macaev, F.; Rusu, G.; Pogrebnoi, S.; Gudima, A.;
- [3] Stingaci, E.; Vlad, L.; Shvets, N.; Kandemirli, F.; Dimoglo, A.; Reynolds, R.
- [4] Bioorg Med Chem 2005, 13, 4842.(c) Zheng, X.; Li, Z.; Wang, Y.; Chen,
- [5] W.; Huang, O.; Liu, C.; Song, C. J Fluorine Chem 2003, 123, 163.
- [6] 2 Bhatt, J. J.; Shah, B. R.; Shah, H. P.; Trivedi, P. B.; Undavia, N. K.; Desai,
- [7] N. C. J Indian Chem 1994, 33B, 189.
- [8] 3 (a) Weaver, G. W. In Science of Synthesis; Storr, R. C.; Gilchrist, T. L.,
- [9] Eds.; Thieme: Stuttgart, 2004; 13, 219; (b) Hill, J.. In Comprehensive
- [10] Heterocyclic Chemistry II; Storr, R. C., Ed. Pergamon, Oxford, 1996; 4,
- [11] 267 and 905 (c) Dobrotã, C.; Paraschivescu, C. C.; Dumitru, I.; Matache,
- [12] M.; Baciu, I.; Rutã, L. L. Tetrahedron Lett 2009, 50, 1886 and references
- [13] therein.
- [14] 4 Bonacorso, H. G.; Paim, G. R.; Porte, L. M. F.; Pittaluga, E. P.; Martins,
- [15] M. A. P., Zanatta, N. ARKIVOC 2012, viii, 214.
- [16] 5 Gaussian 09, Revision A.1, Frisch, M. J. et all Gaussian, Inc., Wallingford
- [17] CT, 2009.
Como citar:
Paim, Gisele R.; Meira, Susiane C.; Pittaluga, Everton P.; Porte, Liliane M. F.; Meyer, Alexandre R.; Navarini, Jussara; Bonacorso, Helio G.; "New 1,3,4-Oxadiazolyl-pyrazolyl-Pyridine Tricyclic Scaffold Derivatives: Synthesis and Structure Assignment by NMR and DFT Calculations", p-142-142.
In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 2, Dezembro.2013.
São Paulo: Blucher,
2013.
ISSN 23184043,
DOI 10.5151/chempro-15bmos-BMOS2013_2013610185416
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TY - CONF T1 - New 1,3,4-Oxadiazolyl-pyrazolyl-Pyridine Tricyclic Scaffold Derivatives: Synthesis and Structure Assignment by NMR and DFT Calculations JO - Blucher Chemistry Proceedings VL - 1 IS - 2 SP - 142 EP - 142 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2013 AU - , , , , , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013610185416 UR - www.proceedings.blucher.com.br/article-details/new-134-oxadiazolyl-pyrazolyl-pyridine-tricyclic-scaffold-derivatives-synthesis-and-structure-assignment-by-nmr-and-dft-calculations-8362 KW - ER -
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@article{Paim20144,
title="New 1,3,4-Oxadiazolyl-pyrazolyl-Pyridine Tricyclic Scaffold Derivatives: Synthesis and Structure Assignment by NMR and DFT Calculations",
journal="Blucher Chemistry Proceedings",
volume="1",
number="2",
pages="142 - 142",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013610185416",
url="www.proceedings.blucher.com.br/article-details/new-134-oxadiazolyl-pyrazolyl-pyridine-tricyclic-scaffold-derivatives-synthesis-and-structure-assignment-by-nmr-and-dft-calculations-8362",
author="Gisele R. Paim", "Susiane C. Meira", "Everton P. Pittaluga", "Liliane M. F. Porte", "Alexandre R. Meyer", "Jussara Navarini", "Helio G. Bonacorso",
keywords="",
}
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Gisele R. Paim, Susiane C. Meira, Everton P. Pittaluga, Liliane M. F. Porte, Alexandre R. Meyer, Jussara Navarini, Helio G. Bonacorso, New 1,3,4-Oxadiazolyl-pyrazolyl-Pyridine Tricyclic Scaffold Derivatives: Synthesis and Structure Assignment by NMR and DFT Calculations, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 142-142, ISSN 23184043, http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013610185416 (www.proceedings.blucher.com.br/article-details/new-134-oxadiazolyl-pyrazolyl-pyridine-tricyclic-scaffold-derivatives-synthesis-and-structure-assignment-by-nmr-and-dft-calculations-8362) Palavras-chave:: ;