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An Expeditious Synthesis of 1,2,4-Triazolo[1,5-a]Pyrimidine
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[1] Syamala M., Org. Prep. Proced. Int. 41 (2009) 1.
[2] Syamala M., Org. Prep. Proced. Int. 37 (2005) 103.
[3] Fischer, G., Adv. Heterocyclic Chem. 57 (1993) 81.
[4] Shaban, M.A.E. Morgan, A.E.A., Adv. in Hetero. Chem. 77 (2000) 345.
[5] Shaban, M.A.E. Morgan, A.E.A. Adv. in Hetero. Chem., 73 (2000) 131.
[6] Shaban, M.A.E. Morgan, A.E.A. Adv. in Hetero. Chem, 75, (2000 ) 243.
[7] Zhang, N. Semiramis, A. K. J. Med. Chem., 50 (2007) 319.
[8] Havlicek, L. Fuksova, K. Krystof, V. Bioorg. And Med. Chem. 13 (2005) 5399.
[9] Fraley M. E., Hoffman W. F. Rubino R. S. Bioorg. And Med. Chem. Lett. 12 (2002) 2767.
[10] Chen, Q. Zhu, X. L. Liu, Z. M. Europ. J. Med. Chem. 43 (2008) 595.
[11] Shaabani A., Farhangi E. Rahmati A., Comb. Chem. 9 (2006) 771.
[12] Heravi M. M., Derikvand F. Ranjbar L., Synth. Commun., 40 (2010) 677.
[13] Lipson V. V., Desenko S. M., Borodina V. V., Musatov V. I., Russ. J. Org. Chem. 41 (2005) 114.
[14] Shankar R. B. Pews R. G., J. Heterocycl. Chem. 30 (1993) 169.
[15] Fedorova O. V., Zhidovinova M. S., Rusinov G. L., Ovchinnikova I. G., Russ. Chem. Bull., Int. Ed. 52, (2003) 1768.
[16] Uryu, S., Tokuhiro, S., Murasugi, T., Brain Research 946 (2002) 298.
[17] Fairfield, B. J.; Andrew, C.; Allan, J. WO2004108136, (2004).
[18] Peng, H., Kumaravel, G., Yao, G., Sha, L., Wang, J., Van Vlijmen, H., Bohnert, T., Huang, C., Vu, C. B., Ensinger, C. L., Chang, H., Engber, T. M., Whalley, E. T., Petter, R. C., J. Med. Chem. 47 (2004) 6218.
DOI: https://doi.org/10.1021/jm0494321