A convenient one-pot synthesis of some new 3-(2-Phenyl-6-(2-thienyl)-4- pyridyl)hydroquinolin-2-ones under microwave irradiation and their antimicrobial activities

Phosphorus, Sulfur and Silicon and the Related Elements

Volumn 185, Issue 3, 2010, Pages 658-662

  Ladani, Niraj K ^a   Patel, Manish P ^a   Patel, Ranjan G ^a  

^a SARDAR PATEL UNIVERSITY   (India)

Author keywords

2 Acetyl thiophene; 2 chloro 3 formyl quinoline; Anti microbial activity; Krohnke reaction condition; Microwave irradiation; Various N phenacylpyridinium bromides

Indexed keywords

EID: 77951234594     PISSN: 10426507     EISSN: 15635325     Source Type: Journal    
DOI: 10.1080/10426500902915507     Document Type: Article

References (33)

1. E. C. Constable, R. M. Manez, A. M. W. C. Thompson, and J. V. Walker, J. Chem. Soc., Dalton Trans., 1585 (1994).
2. I. Eryazici, C. N. Moorefield, S. Drumus, and G. R. Newkome, J. Org. Chem., 71, 1009 (2006).
3. D. Barton and D. Ollis, Comprehensive Organic Chemistry (Pergamon, New York, 1979), vol.4, p. 468.
4. A. R. Katritzky and C. M. Marson, Angew. Chem. Int. Ed. Eng., 23, 420 (1984).
5. G. Jones, A. R. Katritzky, and C. W. Rees, Comprehensive Heterocyclic Chemistry (Pergamon, New York, 1984), vol.2, Part 2A, p. 395.
6. A. Sausins and D. G. Durburs, Heterocycles, 27, 291 (1988).
7. T. Kobayashi and M. Nita, Chem. Lett., 15, 1549 (1986).
8. A. S. Kiselyov, Tetrahedron Lett., 36, 9297 (1995).
9. M. C. G. Barrio, J. R. Barrio, G. Walker, A. Novelli, and N. J. Leonard, J. Am. Chem. Soc., 95, 4891 (1973).
10. F. Krohnke, Angew. Chem. Int. Ed. Engl., 2(5), 225 (1963).
11. F. Krohnke and W. Zecher, Angew. Chem. Int. Ed. Engl., 1(12), 626 (1962).
12. F. Krohnke, Synthesis, 1 (1976);
13. F. Neve, A. Crispini, S. Campagna, Inorg. Chem. 36, 6150 (1997);
14. L. R. Macgillivray, P. R. Diamente, J. L. Reid, J. A. Ipmeester, Chem. Commun. 359, (2000).
15. C. G. Yan, X. M. Cai, Q. F.Wang, T. Y.Wang, andM. Zheng, Org. Biomol. Chem., 5, 945 (2006).
16. X. M. Cai, Q. F. Wang, and C. G. Yan, Synth. Commun., 37, 223 (2007).
17. V. V. Mulwad and D. S. Satwe, Indian J. Chem., 43B, 2727 (2004).
18. B. Kalluraya, J. Nayak, A. Adhikari, K. V. Sujith, N. S. Shetty, and M. Winter, Phosphorus, Sulfur, and Silicon, 183, 1870 (2008).
19. K. Srinivasu, M. Sunilkumar, and A. V. Reddy, Indian J. Chem., 38B, 553 (1999).
20. R. N. Kumar, T. Suresh, and P. S. Mohan, Indian J. Chem., 42B, 688 (2003).
21. L. Perreuex and A. Loupy, Tetrahedron, 57, 9199 (2001).
22. A. R. Desai and K. R. Desai, Arkivoc, xiii, 98 (2005).
23. S. S. Laddha and S. P. Bhatnagar, Phosphorus, Sulfur, and Silicon, 183, 2262 (2008).
24. A. D. Ortiz, F. Lang, A. D. L. Hoz, and A. Moreno, Eur. J. Org. Chem., 4, 3659 (2000).
25. J. H. Clark and D. J. Macquarrie, Chem. Soc. Rev., 25, 303 (1996).
26. C. S. Miller and C. A. Wagner, J. Org. Chem., 13, 89 (1948).
27. O. M. Cohn, B. Narine, and B. Tarnowski, J. Chem. Soc. Perkin Trans I, 1520 (1981).
28. R. K. Bansal and B. Gope, Indian J. Chem., 18B, 362 (1979).
29. S. Tu, R. Jia, B. Jiang, J. Zhang, Y. Zhang, C. Yao, and S. Ji, Tetrahedron, 63, 381 (2007).
30. U. Siemeling, J. V. D. Bruggen, U. Vorfeld, A. Stammler, and H. G. Stammler, Z. Naturforsch, 58b, 443 (2003).
31. A. Srivastava and R. M. Singh, Indian J. Chem., 44B, 1868 (2005).
32. C. H. Collins and P. M. Lyne, Microbial Methods (University Park Press, Baltimore, 1970).
33. T. D. Thangadurai and K. Natarajan, Indian J. Chem., 40A, 573 (2001).