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Warianty tytułu
Języki publikacji
Abstrakty
Keeping the objective to build up a new structural class of quinoxaline, a new series of quinoxaline derivatives bearing the pyridinyl thiazole nucleus have been synthesized by base-catalyzed chloro-amine condensation reaction approach. The protocol offers expeditious and easy synthesis with excellent yield. The chemical structures of the synthesized compounds were elucidated by 1H NMR, 13C NMR, FT-IR, elemental analysis, and mass spectral data.
Słowa kluczowe
Rocznik
Tom
Strony
74--83
Opis fizyczny
Bibliogr. 42 poz., tab., wz.
Twórcy
autor
- Department of Chemistry, Saurashtra University, Rajkot-360005, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot-360005, Gujarat, India
Bibliografia
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- [10] More S. V., Sastry M. N. V., Ching-Fa Y., Green Chem. 8 (2006) 91.
- [11] Patra A. K., Dhar S., Nethaji M., Chakravarty A. R., Dalton Trans. (2005) 896.
- [12] Gobec S., Yamamoto Y., Ed.; Houben Weyl Methods of Molecular Transformations Category 2; Georg Thieme Verlag:Stuttgart-New York, In Science of Synthesis. 16 (2004) 845.
- [13] Kim S. Y., Park K. H., Chung Y. K., Chem. Commun. 10 (2005) 1321.
- [14] Niknam K., Saberi D., Mohagheghnejad M., Molecules. 14 (2009) 1915.
- [15] Hou J.T., Liu Y. H., Zhang Z.H., J. Heterocycl. Chem. 47 (2010) 703;
- [16] Zhang X. Z., Wang J. X., Sun Y. J., Zhan H.W., Chin. Chem. Lett. 21 (2010) 395.
- [17] Lü H.Y., Yang S. H., Deng J. Zhang Z. H., Aust. J. Chem. 63 (2010) 1290.
- [18] Brown D. J., et al., Quinoxalines: Supplement II in The Chemistry of Heterocyclic Compounds, Taylor, E.C.; Wipf, P. (Eds.); John Wiley and Sons: New Jersey; (2004).
- [19] Bhosalea R. S., Sardaa S. R., Ardhapurea S. S., Jadhava W. N., Bhusareb S. R., Pawar R. P.,Tetrahedron Lett. 46 ( 2005) 7183.
- [20] Bhosale R. S., Sarda S. R., Ardhapure S. S., Jadhav W. N., Bhusare S. R., Pawar R. P., Tetrahedron Lett. 46 (2005) 7183.
- [21] More S. V., Sastry M. N. V., Wang C. C., Yao C. F., Tetrahedron Lett. 46 (2005) 6345.
- [22] Darabi H. R., Mohandessi S., Aghapoor K., Mohsenzadeh F., Catal. Commun. 8 (2007) 389.
- [23] Huang T. K., Wang R., Shi L., Lu X. X., Catal. Commun. 9 ( 2008) 1143.
- [24] Srinivas C., Kumar C. N. S. S. P., Jayathirtha Rao V., Palaniappan S., J. Mol. Catal. A: Chem. 265 (2007) 227.
- [25] Heravi M. M., Bakhtiari Kh., Bamoharram F. F., Tehrani, M. H., Monatsh. Chem. 138 (2007) 465.
- [26] Hazarika P., Gogoi P., Konwar D., Synth. Commun. 37 (2007) 3447.
- [27] Heravi M. M., Bakhtiari Kh., Oskooie H. A., Taheri Sh., Heteroat. Chem. 19 (2008) 218.
- [28] Heravi M. M., Taheri Sh., Bakhtiari Kh., Oskooie H. A., Catal. Commun. 8 (2007) 211.
- [29] Heravi M. M., Tehrani M. H., Bakhtiari Kh., Oskooie H. A., Catal. Commun. 8 (2007) 1341.
- [30] More S. V., Sastry M. N. V., Yao C. F., Green Chem. 8 (2006) 91.
- [31] Antoniotti S., Donach E., Tetrahedron Lett. 43 (2002) 3971.
- [32] Robinson R. S., Taylor R. J. K., Synlett. (2005) 1003.
- [33] Raw S. A., Wilfred C. D., Taylor R. J. K., Org. Biomol. Chem. 2 (2004) 788.
- [34] Raw S. A., Wilfred C. D., Taylor R. J. K., Chem. Commun. (2003) 2286.
- [35] Zhao Z., Wisnoski D. D., Wolkenberg S. E., Leister W. H., Wang Y., Lindsley C. W., Tetrahedron Lett. 45 (2004) 4873.
- [36] Dodson R. M., King L. C., J Am Chem Soc. 67 (1945) 2242.
- [37] Khunt H., Pipaliya P., Ghelani S., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 24 (2014) 134.
- [38] Patel A. S., Khunt H., Babariya J., Ghelani S., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 30 (2014) 106.
- [39] Gami P., Vilapara K., Khunt H., Babariya J., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 30 (2014) 127.
- [40] Khunt H., Babariya J., Dedakiya C., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 30 (2014) 185.
- [41] Khunt H., Babariya J., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 31 (2014) 20.
- [42] Prajapati D., Vilapara K., Naliapara Y. T., International Letters of Chemistry, Physics and Astronomy 33 (2014) 12.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-20d49822-c826-4d75-b06f-2d87e2bc233e