Synthesis and characterization of a series of 1,3,5-trisubstituted-2-pyrazolines derivatives using methanoic acid under thermal condition

Journal of the Serbian Chemical Society

Volumn 74, Issue 12, 2009, Pages 1371-1376

  Maleki, Behrooz ^a   Azarifar, Davood ^b   Moghaddam, Mona Khodaverdian ^a   Hojati, Seyedeh Fatemeh ^a   Gholizadeh, Mostafa ^a   Salehabadi, Hafezeh ^a  

^a HAKIM SABZEVARI UNIVERSITY   (Iran)

^b BU ALI SINA UNIVERSITY   (Iran)

Author keywords

1,3,5 trisubstituted 2 pyrazoline; Chalcone; Heterocyclic synthesis; Methanoic acid; Phenylhydrazine

Indexed keywords

EID: 77349127337     PISSN: 03525139     EISSN: None     Source Type: Journal    
DOI: 10.2298/JSC0912371M     Document Type: Article

References (26)

1. L. W. Wattenberg, M. A. Page, J. L. Leong, Cancer Res. 28 (1968) 2539
2. T. Shah, V. Desi, J. Serb. Chem. Soc. 72 (2007) 443
3. S. Mostahar, S. Alam, A. Islam, J. Serb. Chem. Soc. 72 (2007) 329
4. V. N. Patange, R. K. Pardeshi, B. R. Arbad, J. Serb. Chem. Soc. 73 (2008) 1073
5. M. S. Yar, A. A. Siddqui, M. S. Ali, J. Serb. Chem. Soc. 72 (2007) 5
6. E. Taylor, H. Patel, H. Kumar, Tetrahedron 48 (1992) 8089
7. M. S. Karthikeyan, B. S. Holla, N. S. Kumari, Eur. J. Med. Chem. 42 (2007) 30
8. B. S. Holla, P. M. Akberali, M. K. Shivananda, Farmaco 55 (2000) 256
9. E. Bansal, V. K. Srivatsava, A. Kumar, Eur. J. Med. Chem. 36 (2001) 81
10. F. Manna, F. Chimenti, R. Fioravanti, A. Bolasco, D. Secci, P. Chimenti, C. Ferlini, G. Scambia, Bioorg. Med. Chem. Lett. 15 (2005) 4632
11. J. H. Ahn, H. M. Kim, S. H. Jung, S. K. Kang, K. R. Kim, S. D. Rhee, S. D. Yang, H. G. Cheon, S. S. Kim, Bioorg. Med. Chem. Lett. 14 (2004) 4461
12. Y. R. Prasad, R. A. Lakshmana, L. Prasoona, K. Murali, K. P. Ravi, Bioorg. Med. Chem. Lett. 15 (2005) 5030
13. J. Elguero, in Comprehensive Heterocyclic Chemistry, Vol. 5, A. R. Katritzky, C. W. Rees, Eds., Pergamon Press, Oxford, 1984, pp. 167-302
14. J. Elguero, in Comprehensive Heterocyclic Chemistry II, A. R. Katritzky, C. W. Rees, E. F. Scriven, Eds., Pergamon Press, Oxford, 1996, pp. 1-75
15. V. V. Dabholkar, R. P. Gavande, J. Serb. Chem. Soc. 68 (2003) 723
16. A. Levai, Arkivoc 9 (2005) 344
17. J. T. Li, X. H. Zhang, Z. P. Lin, Beilstein J. Org. Chem. 3 (2007) 1
18. R. R. Kamble, B. S. Sudha, D. G. Bhadregowda, J. Serb. Chem. Soc. 73 (2008) 131
19. D. Azarifar, M. Saebanzadeh, Molecules 7 (2002) 885
20. D. Azarifar, H. Ghasemnejad, Molecules 8 (2003) 642
21. D. Azarifar, B. Maleki, J. Heterocycl. Chem. 52 (2005) 157
22. W. Reutemann, H. Kieczka, in Ullmann's Encyclopedia of Industrial Chemistry, 5th Ed., VCH, Weinheim, 1983, pp. 13-33
23. H. W. Gibson, Chem. Rev. 69 (1969) 673
24. R. A. W. Johnstone, A. H. Wilby, I. D. Entwistle, Chem. Rev. 85 (1985) 129
25. G. Brieger, T. J. Nestrick, Chem. Rev. 74 (1974) 567
26. H. S. P. Rao, S. Jothilingam, K. Vasantham, H. W. Scheeren, Tetrahedron Lett. 48 (2007) 4495.