Synthesis and antimicrobial activity of some novel 2-(substituted fluorobenzoylimino)-3-(substituted fluorophenyl)-4-methyl-1,3-thiazolines

Journal of Fluorine Chemistry

Volumn 131, Issue 3, 2010, Pages 333-339

  Saeed, Aamer ^a   Shaheen, Uzma ^a   Hameed, Abdul ^a   Kazmi, Faiza ^a  

^a QUAID I AZAM UNIVERSITY   (Pakistan)

Author keywords

3 Thiazolines; Antimicrobial activity; Fluorinated 1,3 disubstituted thioureas; Fluorinated imino 1

Indexed keywords

EID: 76549125932     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2009.11.005     Document Type: Article

References (28)

1. Dolbier Jr. W.R. J. Fluorine Chem. 126 (2005) 157-163
2. Antelo J.M., Crugeiras J., Leis J.R., and Rios A. J. Chem. Soc., Perkin Trans. 2 (2000) 2071-2076
3. Edwards P.N. Uses of fluorine in chemotherapy. In: Banks R.E., Smart B., and Tatlow J.C. (Eds). Organofluorine Chemistry: Principles and Commercial Applications (1994), Plenum Press, New York 543-554
4. Wakselman C. Ann. Pharm. Fr. 57 (1999) 108-115
5. Smart B.E. J. Fluor. Chem. 109 (2001) 3-11
6. Vicini P., Geronikaki A., Anastasia K., Incerti M., and Zani F. Bioorg. Med. Chem. 14 (2006) 3859-3864
7. Zhang A., Kaiser H., Maienfisch P., and Casida J.E. J. Neurochem. 75 (2000) 1294-1303
8. Maienfisch P., Haettenschwiler J., Rindlisbacher A., Decock A., Wellmann H., and Kayser H. Chimia 57 (2003) 710-714
9. Hosseinimehr S.J., Shafiee A., Mozdarani H., and Akhlagpour S. J. Radiat. Res. 42 (2001) 401-408
10. Hosseinimehr S.J., Shafiee A., Mozdarani H., Akhlagpour S., and Froughizadeh M. J. Radiat. Res. 43 (2002) 293-300
11. Bae S., Hahn H.-G., and Nam K.D. J. Comb. Chem. 7 (2005) 7-12
12. Kim D.-S., Jeong Y.-M., Park I.-K., Hahn H.-G., Lee H.-K., Kwon S.-B., Yang S.J., Sohn U.D., and Park K.-C. Biol. Pharm. Bull. 30 (2007) 180-183
13. Nicolas P., Anice M., Rosanna D., Paul L., Veronique P., Fabienne L., Mathias B., Jean-Louis K., and Flavio M. J. Med. Chem. 49 (2006) 3645-3652
14. Sondhi S.M., Singh S., Kumar J., Jamal H., and Gupta P.P. Eur. J. Med. Chem. 44 (2009) 1010-1015
15. Manaka A., Sato M., Aoki M., Tanaka M., Ikeda T., Toda Y., Yamanane Y., and Nakaike S. Bioorg. Med. Chem. Lett. 11 (2001) 1031-1035
16. Sondhi S.M., Singh N., Lahoti A.M., Bajaj K., Kumar A., Lozach O., and Meijer L. Bioorg. Med. Chem. 13 (2005) 4291-4299
17. Shih M.-H., and Ke F.-Y. J. Bioorg. Med. Chem. 12 (2004) 4633-4638
18. Sanemitsu Y., Kawamura S., Satoh J., Katayama T., and Hashimoto S. J. Pestic. Sci. 31 (2006) 305-310
19. Aly A.A., Ahmed E.K., and El-Mokadem K.M. J. Sulfur Chem. 27 (2006) 419-426
20. Zeng R.-S., Zou J.-P., Zhi S.-J., Chen J., and Shen Q. Org. Lett. 5 (2003) 1657-1659
21. Singh C.B., Murru S., Kavala V., and Patel B.K. Org. Lett. 8 (2006) 5397-5399
22. Germanas J.P., Wang S., Miner A., Hao W., and Ready J.M. Bioorg. Med. Chem. Lett. 17 (2007) 6871-6875
23. Demko Z.P., and Sharpless K.B. Org. Chem. 66 (2001) 7945-7951
24. Li C.J. Chem. Rev. 105 (2005) 3095-4007
25. Rispens T., and Engberts J.B.F.N. J. Org. Chem. 67 (2001) 7369-7372
26. Yadav J.S., Swami S.T., Reddy B.V.S., and Krishna Rao D. J. Mol. Catal. A: Chem. 274 (2007) 116-126
27. Saeed A., Zaman S., and Bolte M. Synth. Commun. 38 (2008) 2185-2199
28. Saeed A., and Parvez M. Cent. Eur. J. Chem. 3 (2005) 780-791