Warianty tytułu
Języki publikacji
Abstrakty
A convenient synthesis of substituted 1,2,4-triazolo[1,5-a]pyrimidine was carried out by the reaction of various ketene dithioacetals with 5-amino 1,2,4-triazole in methanol in presence of sodium methoxide. The newly synthesized compound were characterized by 1H NMR, 13C NMR, IR, MS, elemental analysis and screened for their antimicrobial activity against various strains of bacteria and fungi.
Rocznik
Tom
Strony
127-134
Opis fizyczny
Bibliogr. 22 poz., tab., wz.
Twórcy
autor
- Department of Chemistry, Saurashtra University, Rajkot-36005, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot-36005, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot-36005, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot-36005, Gujarat, India
autor
- Department of Chemistry, Saurashtra University, Rajkot-36005, Gujarat, India, naliaparachem@yahoo.co.in
Bibliografia
- [1] G. Fischer, Adv. Heterocycl. Chem. 57 (1993) 81.
- [2] M. Shaban, A. Morgan, Adv. Heterocycl. Chem. 77 (2000) 345.
- [3] M. Shaban, A. Morgan, Adv. Heterocycl. Chem., 73 (2000) 131.
- [4] M. Shaban, A. Morgan, Adv. Heterocycl. Chem. 75 (2000) 243.
- [5] N. Zhang, A. Semiramis, N. Thai, J. Med. Chem. 50 (2007) 319.
- [6] L. Havlicek; K. Fuksova; V. Krystof, Bioorg. Med. Chem. 13 (2005) 5399.
- [7] X. Zhao; Y. Zhao; S. Guo; H. Song; D. Wang; P. Gong, Molecules 12 (2007) 1136.
- [8] L. Iwona, F. Marzena, M. Tadeusz, S. Tadeusz, J. Julia, Dalton Trans. 42 (2013) 6219.
- [9] A. Marwaha, J. White, F. El Mazouni, S. Creason, S. Kokkonda, F. Buckner, P. Rathod, J. Med. Chem. 55 (2012) 7425.
- [10] L. Yin; Z. Shuai; L. Zhi-Jun; Z. Hai-Liang, Euro. J. Med. Chem. 64 (2013) 54.
- [11] H. Ashraf, Abd El-Wahab Pharmaceuticals 5 (2012) 745.
- [12] A. Abdel-Aziem, M. Sayed El-Gendy, A. Abdelhamid, Euro. J. Chem. 3 (2012) 455.
- [13] M. Khera, I. Cliffe, T. Mathur, O. Prakash, Bioorg. Med. Chem. Lett. 21 (2011) 2887.
- [14] H. Ashour, O. Shaaban, O. Rizk, I. El-Ashmawy, Euro. J. Med. Chem. 62 (2013) 341.
- [15] M. Fraley, W. Hoffman, R. Rubino, Bioorg. Med. Chem. Lett. 12 (2002) 2767.
- [16] Q. Chen, X. Zhu, Z. Liu, Euro. J. Med. Chem. 43 (2008) 595.
- [17] S. Uryu, S. Tokuhiro, T. Murasugi, Brain Research 946 (2002) 298
- [18] L. Antonino, A. Ilenia, P. Chiara, M. Annamaria, D. Gaetano, A. Maria, Euro. J. Med. Chem. 62 (2013) 416.
- [19] B. Fairfield, C. Andrew, J. Allan, WO2004108136, (2004).
- [20] C. Tamilselvan, S. John Joseph, G. Mugunthan, S. Syed Musthaq Ahamed, International Letters of Chemistry, Physics and Astronomy 9 (2014) 93-102.
- [21] R. G. Vaghasiya, H. B. Ghodasara, P. R. Vachharajani, V. H. Shah, International Letters of Chemistry, Physics and Astronomy 8 (2014) 30-37.
- [22] Piyush B. Vekariya, Jalpa R. Pandya, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 7 (2014) 45-52.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.baztech-6e83aa9b-fb67-4661-96c9-c8b9ad673baf