PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Synthesis and antimicrobial screening of some new pyrimido[1,2-a]benzimidazole derivatives

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Some new pyrimido[1,2-a]benzimidazole derivatives were synthesized by reacting 2-amino benzimidazole and chalcones in n-butanol at reflux temperature. In our present study we have used various heterocyclic chalcones derived from furfural and substituted acetophenones. All synthesized compounds were characterized by IR, 1H NMR and Mass spectroscopy. All synthesized compounds were screened for their antimicrobial activity against gram positive and gram negative bacteria which showed moderate to good activity.
Rocznik
Tom
Strony
56--60
Opis fizyczny
Bibliogr. 21 poz., rys., tab.
Twórcy
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360 005, Gujarat, India
Bibliografia
  • [1] Q. McKellar, E. Scott, J. Vet. Pharmacol. Ther. 13 (1990) 223.
  • [2] A. Spasov, I. Yozhitsa, L. Bugaeva, V. Anisimova, Pharm. Chem. J. 33 (1999) 232.
  • [3] J. Rossignol, H. Maisonneuve, Ann. Trop. Med. Parasitol. 78 (1984) 135
  • [4] A. Patil, S. Ganguly, S. Surana, Rasayan J. Chem. 1 (2008) 447.
  • [5] A. Dubey, P. Sanyal, Online Vet. J. 5 (2010) 63.
  • [6] M. Boiani, M. Gonzalez, Mini Rev. Med. Chem. 5 (2005) 409.
  • [7] B. Narasimhan, D. Sharma, P. Kumar, Med. Chem. Res. 21 (2012) 269.
  • [8] Y. Fellahi, P. Dubois, V. Agafonov, F. Moussa, J. E. Ombetta-Goka, J. Guenzet, Y. Frangin, Bull. Soc. Chim. Fr. 133 (1996) 869.
  • [9] J. Kempson, et. al., Bioorg. Med. Chem. Lett. 15 (2005) 1829.
  • [10] V. Chebanov, S. Desenko, Curr Org Chem 10 (2006) 297.
  • [11] S. Desenko, Chem Heterocycl Comp 31 (1995) 125.
  • [12] P. Zalavadiya, S. Tala, J. Akbari, H. Joshi, Archiv der Pharmazie 342 (2009) 469.
  • [13] R. Khunt, J. Akbari, A. Manvar, S. Tala, M. Dhaduk, H. Joshi, A. Shah, Arkivoc 11 (2008) 277.
  • [14] P. Zalavadiya, R. Ghetiya, B. Dodiya, P.Vekariya, H. Joshi, Journal of Heterocyclic Chemistry 50 (2013) 973.
  • [15] S. Rokad, S. Tala, J. Akbari, M. Dhaduk, H. Joshi, Journal of the Indian Chemical Society 86 (2009) 186.
  • [16] S. Tala, P. Vekariya, R. Ghetiya, B. Dodiya, H. Joshi, Indian Journal of Chemistry 52 (2013) 807.
  • [17] G. Thirunarayanan, M. Suresh, International Letters of Chemistry, Physics and Astronomy 4 (1) (2014) 1-11.
  • [18] K. G Sekar, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 8(3) (2013)249-258.
  • [19] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.
  • [20] K. G. Sekar, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 8(2) (2013) 160-174.
  • [21] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 4 (2014) 109-116.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-32b32ede-b7f5-4b2b-81fd-6b6575143629
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.