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Synthesis, characterization and biological evaluation of 2,5-di-substituted 1,3,4-oxadiazole derivatives

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
We have reported some novel 1,3,4-oxadiazole synthesized by conventional method .The reaction of 5-bromothiophene-2-carbohydrazide and different benzoic acid derivatives reflux in toluene using phosphorus oxychloride as a catalyst, yielded a series of 2,5-di-substituted 1,3,4-oxadiazole HM-2a to HM-2t. The newly synthesized 2,5-di-substituted 1,3,4-oxadiazole were purified by column chromatography and characterized by IR, Mass, 1H NMR, 13C NMR spectroscopy and elemental analysis. All synthesized compounds were screened for antimicrobial activity using cup plate method. All the compounds showed moderate to good antimicrobial activity and anti fungal activity.
Rocznik
Tom
Strony
48--54
Opis fizyczny
Bibliogr. 15 poz., tab., wz.
Twórcy
autor
  • Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
  • Department of Chemistry, Saurashtra University, Rajkot, Gujarat, India
Bibliografia
  • [1] Potts, K. In Compr. Heterocyclic Chem.; Katritzky, A.R., Rees, Ch., Eds.; Pergamon Press: NY; 6 (1984) 427.
  • [2] Kulkarni Y. D., Rowhani A., J. Indian Chem. Soc. 66 (1989) 492.
  • [3] Mohamed Ashraf Ali, Mohammad Shaharyar, Bioorganic & Medicinal Chemistry Letters 17 (2007) 3314-3316.
  • [4] Neelam Jain, D. P. Pathak, Pradeep Mishra, Sandeep Jain, Der Pharmacia Lettre, 5 (2013) 415-418.
  • [5] S. L. Gaonkar, K. M. L. Rai, B. Prabhuswamy, Eur. J. Med. Chem. 41 (2006) 841-846.
  • [6] Zampieri D., et al., Bioorg. Med. Chem. 17 (2009) 4693-4707.
  • [7] B. Chandrakantha, Prakash Shetty, Vijesh Nambiyar, Nishitha Isloor, Arun M. Isloor, European Journal of Medicinal Chemistry 45 (2010) 1206-1210.
  • [8] Samir Bondock, Shymaa Adel, Hassan A. Etman, Farid A. Badria; European Journal of Medicinal Chemistry 48 (2012) 192-199.
  • [9] Rajesh A. Rane, Pavankumar Bangalore, Sheetal D. Borhade, Preeti K. Khandare, European Journal of Medicinal Chemistry 70 (2013) 49-58.
  • [10] Jansen M., et al., H. J. Med. Chem. 51 (2008) 4430-4448.
  • [11] P. C. Unangast, G. P. Shrum, D. T. Conner, C. D. Dyer, D. J. Schrier, J. Med. Chem. 35 (1992) 3691-3698.
  • [12] V. Ravichandran, S. Shalini, K. Sundram, A. Dhanaraj Sokkalingam, European Journal of Medicinal Chemistry 45 (2010) 2791-2797.
  • [13] Omar F. A., Mahfouz N. M., Rahman, M. A., Eur. J. Med. Chem.Chim. Ther. 31 (1996) 819.
  • [14] Dipti L. Namera, Jaynt B. Rathod, Rupali H. Maheta, Umed C. Bhoya, International Letters of Chemistry, Physics and Astronomy 10 (2014) 46-54.
  • [15] Dipti L. Namera, Umed C. Bhoya, International Letters of Chemistry, Physics and Astronomy, 11(2) (2014) 159-166.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-4e3c4e58-c0b6-4ec7-ac30-9e1f25bce1e9
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