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Some new 2-azetidinone derivatives possessing benzimidazole nucleus were synthesized and characterized by IR, NMR and mass spectral 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.
Słowa kluczowe
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Tom
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81--88
Opis fizyczny
Bibliogr. 21 poz., tab., wz.
Twórcy
autor
- Home Science Department, Dr. Subhash Mahila Arts, Commerce & Home Science College,Junagadh - 362 001, Gujarat
autor
- Chemical Research Laboratory, Department of Chemistry, Saurashtra University, Rajkot - 360005, India
autor
- Chemical Research Laboratory, Department of Chemistry, Saurashtra University, Rajkot - 360005, India
autor
- Chemical Research Laboratory, Department of Chemistry, Saurashtra University, Rajkot - 360005, 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] M. Gaba, S. Singh, C. Mohan, Eur. Jour. Med. Chem. (2014) doi: 10.1016/ j.ejmech.2014.01.030.
- [5] N. C. Desai, D. D. Pandya, G. M. Kotadiya, P. Desai, Med.Chem.Res. 23 (2014) 1725-1741.
- [6] M. Grare, M. Mourer, S. Fontanay, J. B. Regnouf-de-Vains, C. Finance, J Antimicrob Chemother. 60 (2007) 575-581.
- [7] G. I. Georg (ed) (1993). The organic chemistry of β-lactams. VCH, New York.
- [8] P. D. Buttero, G. Molteni, T. Pilati, Tett. Lett. 44 (2003) 1425-1427.
- [9] D. K. Shukla, S. D. Srivastava, Indian J. Chem. 47B (2008) 463.
- [10] V. V. Mulwad, A. A. Mir, J. Korean Chem. Soc. 52 ( 2008) 649.
- [11] A. K. Parikh, P. S. Oza, S. B. Bhatt, Indian J. Chem. 44B (2005) 585.
- [12] S. K. Srivastava, S. Srivastava, S. D. Srivastava, Indian J. Chem. 38B (2000) 464.
- [13] S. K. Srivastava, S.L. Srivastava, S. D. Srivastava, Indian J. Chem. 39B (1999) 183.
- [14] J. W. Skiles, D. McNeil, Tetrahedron Lett. 31 (1990) 7277.
- [15] B. S. Vashi, D. S. Mehta, V. H. Shah, Indian J. Chem. 34B (1995) 802.
- [16] G. Wu, W. Tormos, J. Org. Chem. 62 (1997) 6412.
- [17] R. E. Miller, R. S. Brandt. J. Bact. 38 (1939) 539-547.
- [18] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.
- [19] Mita D. Khunt, Vipul C. Kotadiya, Denish J. Viradiya, Bharat H. Baria, Umed C. Bhoya, International Letters of Chemistry, Physics and Astronomy 6 (2014) 61-68.
- [20] Prakash Mehta, Prakash Davadra, Nirav Shah, Hitendra Joshi, International Letters of Chemistry, Physics and Astronomy 10 (2014) 74-80.
- [21] Prakash Mehta, Prakash Dawedra, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 11(1) (2014) 1-8.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-1e05da1b-35a7-4b8a-ab12-b7ed53960252