JOURNAL BROWSE
Search
Advanced SearchSearch Tips
An Expeditious Room Temperature Stirring Method for the Synthesis of Isoxazolo[5,4-b]quinolines
facebook(new window)  Pirnt(new window) E-mail(new window) Excel Download
 Title & Authors
An Expeditious Room Temperature Stirring Method for the Synthesis of Isoxazolo[5,4-b]quinolines
Niralwad, Kirti S.; Shingate, Bapurao B.; Shingare, Murlidhar S.;
  PDF(new window)
 Abstract
The synthesis of different derivatives of isoxazolo[5,4-b]quinoline by the cyclization reaction of various substituted oximes of quinoline using mild base at ambient temperature. The formation of isoxazolo[5,4-b]quinoline, as a consequence of cheaper and more readily available and DMF participating in the reaction, is documented.
 Keywords
Isoxazolo[5,4-b]quinoline;;Room temperature;
 Language
English
 Cited by
1.
Direct synthesis of 4-organylsulfenyl-7-chloro quinolines and their toxicological and pharmacological activities in Caenorhabditis elegans, European Journal of Medicinal Chemistry, 2014, 75, 448  crossref(new windwow)
 References
1.
Cohn, O. M.; Narine, B.; Tarnowski, B. J. Chem. Soc. Perkin Trans. 1981, 1, 1520.

2.
Michael, J. P.; Nat. Prod. Rep. 2008, 25, 166. crossref(new window)

3.
Michael, J. P. Nat. Prod. Rep. 2007, 24, 223. crossref(new window)

4.
Kouznetsov, V. V.; Vargas L. Y.; Mendez, C. M.; Melendez Gomez Curr. Org. Chem. 2005, 9, 141. crossref(new window)

5.
Michael, J. P. Nat. Prod. Rep. 2004, 21, 650. crossref(new window)

6.
Michael, J. P. Nat. Prod. Rep. 2005, 22, 627. crossref(new window)

7.
Chen, Y. L.; Fang, K. C.; Sheu, J. Y.; Hsu, S. L.; Tzeng, C. C. J. Med. Chem. 2001, 44, 2374. crossref(new window)

8.
Roma, G.; Braccio, M. D.; Grossi, G.; Mattioli, F.; Ghia, M. Eur. J. Med. Chem. 2000, 35 1021. crossref(new window)

9.
Doube, D.; Blouin, M.; Brideau, C.; Desmarais, C.; Chan, S.; Eithier, D.; Fagueyret, J. P.; Friesen, R. W.; Girard, M.; Girard, Y.; Guay, J.; Tagari, P.; Young, R. N. Bioorg. Med. Chem. Lett. 1998, 8, 1255. crossref(new window)

10.
Larsen, R. D.; Corley, E. G.; King, A. O.; Carrol, J. D.; Davis, P.; Verhoeven, T. R.; Reider, P. J.; Labelle, M.; Gauthier, J. Y.; Xiang, Y. B.; Zamboni R. J.; J. Org. Chem. 1996, 61, 3398. crossref(new window)

11.
Bringmann, G.; Reichert, Y.; Kane, V. Tetrahedron 2004, 60, 3539. crossref(new window)

12.
Ko, T. C.; Hour, M. J.; Lien, J. C.; Teng, C. M.; Lee, K. H.; Kuo, S. C.; Huang, L. J. Bioorg. Med. Chem. Lett. 2001, 11, 279. crossref(new window)

13.
Ferrarini, P. L.; Mori, C.; Badwneh, M.; Manera, C.; Martinelli, A.; Miceli, M.; Ramagnoli, F.; Saccomanni, G. J. Heterocycl. Chem. 1997, 34, 1501. crossref(new window)

14.
Maguire, M. P.; Sheets, K. R.; McVety, K.; Spada, A. P.; Zilberstein, A. J. Med. Chem. 1994, 37, 2129. crossref(new window)

15.
Cairns, H.; Cox, D.; Gould, K. J.; Ingall, A. H.; Suschitzky, J. L. J. Med. Chem. 1985, 28, 1832. crossref(new window)

16.
Croisy-Delcey, M.; Coroisy, A.; Carrez, D.; Huel, C.; Chiaroni, A.; Ducrot, P.; Bisagni, E.; Jin, L.; Leclercq, G. Bioorg. Med. Chem. 2000, 8, 2629. crossref(new window)

17.
Abadi, A. H.; Brun, R. Arzneimforsch Drug Res. 2003, 53, 655.

18.
Maguire, M. P.; Sheets, K. R.; McVety, K.; Spada, A. P.; Zilberstein, A. J. Med. Chem. 1994, 37, 2129. crossref(new window)

19.
Larsen, R. D.; Corley, E. G.; King, A. O.; Carroll, J. D.; Davis, P.; Verhoeven, T. R.; Reider, P. J.; Labelle, M.; Gauthier, J. Y.; Xiang, Y. B.; Zamboni, R. J.; J. Org. Chem. 1996, 61, 3398. crossref(new window)

20.
Kalluraya, B.; Sreenivasa, S.; Farmaco. 53, 1998, 399. crossref(new window)

21.
Doube, D.; Blouin, M.; Brideau, C.; Chan, C.; Desmarais, S.; Eithier, D.; Falgueyret, J. P.; Friesen, R. W.; Girrard, M.; Girard, Y.; Guay, J.; Tagari, P.; Young, R. N. Bioorg. Med. Chem. Lett. 1998, 8, 1255. crossref(new window)

22.
Roma, G.; Braccio, M. D.; Grossi, G.; Mattioli, F.; Ghia, M. Eur. J. Med. Chem. 2000, 35, 1021. crossref(new window)

23.
Gabriele, B.; Mancuso, R.; Salerno, G.; Ruffolo, G.; Plastina, P. J. Org. Chem. 2007, 72, 6873. crossref(new window)

24.
Padwa, A.; Brodney, M. A.; Liu, B.; Satake, K.; Wu, T. J. Org. Chem. 64, 1999, 3595. crossref(new window)

25.
Robert, A.; Meunier, B. Chem. Soc. Rev. 1998, 27, 273. crossref(new window)

26.
Patel, H. V.; Vyas, K. V.; Fernandes, P. S. Indian J. Chem. 1990, 29B, 836.

27.
Craig, J. C.; Person, P. E. J. Med. Chem. 1971, 14, 1221. crossref(new window)

28.
Dillard, R. D.; Pravey, D. E.; Benslay, D. N. J. Med. Chem. 1973, 16, 251. crossref(new window)

29.
Huma, H. Z.; Halder, S. R.; Kalar, S. S.; Das, J.; Iqbal, J. Tetrahedron Lett. 2002, 43, 6485. crossref(new window)

30.
Yadav, J. S.; Reddy, B. V. S.; Rao, R. S.; Naveenkumar, V.; Nagaiah, K. Synthesis 2003, 10, 1610.

31.
Wang, Y. L.; Zhu, S. Z. Synthesis 2002, 13, 1813.

32.
MethCohn, O.; Narine, B.; Tarnowski, B.; Hayes, R.; Keyzad, A.; Rhouti, S.; Robinson, A.; J. Chem. Soc. Perkin Trans 1 1981, 2509.

33.
Bhaduri, A. P. Synlett 1990, 557.

34.
Fries, R. W.; Bohiken, D. P.; Plapp, B. V. J. Med. Chem. 1979, 22, 356. crossref(new window)

35.
Secor, H. V.; De Bordeleben J. F. J. Med. Chem. 1971, 14, 997. crossref(new window)

36.
Burger S. Med. Chem. 4th ed.; Wiley: New York, 1971.

37.
Picciola, G.; Ravenna, F.; Carenini, G.; Gentili, P.; Riva, M. Farmaco Ed. Sci. 1981, 36, 1037.

38.
Kuhnert-Brandstaetter M. Pharm Sci. 1971, 39, 15.

39.
Kidwai, M., Negi, N. Monatshefte fir Chemie 1997, 128, 85. crossref(new window)

40.
Thore, S. N.; Shinde, D. B.; Shingare, M. S. Oriental J. Chem. 1995, 11, 135.

41.
Gawande, N. G.; Shingare, M. S Indian J. Chem. 1987, 26B, 351.

42.
Niralwad, K. S.; Shelke, K. F.; Sadaphal, S. S.; Shingate, B. B.; Shingare, M. S. Bull. Korean Chem. Soc. 2010, 31, 981. crossref(new window)

43.
Sapkal, S. B.; Shelke, K. F.; Shingate, B. B.; Shingare, M. S. Tetrahedron Lett. 2009, 50, 1754. crossref(new window)

44.
Niralwad, K. S. Shelke, K. F.; Sadaphal, S. S.; Shingate, B. B.; Shingare, M. S. Ultrasonics Sonochem. 2010, 17, 760. crossref(new window)