ZrP2O7 nanoparticles as a robust and efficient catalyst for the synthesis of 2-aryl-5-methyl-2,3-dihydro-1H-3-pyrazolones under microwave irradiation

Subject Areas : Iranian Journal of Catalysis

Javad Safaei-Ghomi ¹ , Esmaeil Afkhami ² , Hossein Shahbazi-Alavi ³ , Abolfazl Ziarati ⁴

1 - Department of Chemistry, Qom Branch, Islamic Azad University, Qom, Iran.
2 - Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan, P.O. Box 87317-51167, Iran.
3 - Department of Chemistry, Qom Branch, Islamic Azad University, Qom, Iran.
4 - School of Chemistry, College of Science, University of Tehran, Tehran 14155-6455, Iran.

Received: 2015-02-09 Accepted : 2015-05-12 Published : 2015-12-01

Keywords:

References:

[1] D. Castagnolo, F. Manetti, M. Radi, B. Bechi, M. Pagano, A.D. Logu, R. Meleddu, M. Saddi, M. Botta, Bioorg. Med. Chem. 17 (2009) 5716–5721.
[2] A. Gürsoy, S. Demirayak, G. Çapan, K. Erol, K. Vural, Eur. J. Med. Chem. 35 (2000) 359−364.
[3] E.S.A.M. Badaweya, I.M. El-Ashmawey, Eur. J. Med. Chem. 33 (1998) 349-361.
[4] R. Verma, P. Chawla, S.K. Saraf, Pharm. Sin. 3 (2012) 546-555.
[5] R.B. Shete, R.V. Antre, R.J. Oswal, S.S. Kshirsagar, S.S. Jangam, H.M. Nimje, Inter. J. Drug Design Disc. 2 (2011) 648-653.
[6] F. Moreau, N. Desroy, J.M. Genevard, V. Vongsouthi, V. Gerusz, G.L. Fralliec, C. Oliveira, S. Floquet, A. Denis, S. Escaich, K. Wolf, M. Busemann, A. Aschenbrenner, Bioorg. Med. Chem. Lett. 18 (2008) 4022–4026.
[7] A. Dastan, A. Kulkarni, B. Török, Green Chem. 14 (2012)17-37.
[8] M.S. Singh, S. Chowdhury, RSC Adv. 2 (2012) 4547-4592.
[9] F. Yu, R. Huang, H. Ni, J. Fan, S. Yan, J. Lin, Green Chem. 15 (2013) 453-462.
[10] Z. Xu, F. D. Moliner, A.P. Cappelli, C. Hulme, Org. Lett. 15 (2013) 2738–2741.
[11] K. Chanda, S. Rej, M.H. Huang, Chem. Eur. J. 19 (2013)16036 –16043.
[12] A.J.V. Wangelin, H. Neumann, D. Grdes, S. Klaus, D. Strübing, M. Beller, Chem. Eur. J. 9 (2003) 4286-
4294.
[13] N. Isambert, M.M.S. Duque, J.C. Plaquevent, Y. Genisson, J. Rodriguez, T. Constantieux, Chem. Soc. Rev. 40 (2011) 1347–1357.
[14] A. Bhunia, T. Kaicharla, D. Porwal, R. G. Gonnade, A. T. Biju, Chem. Commun. 50 (2014) 11389-
11392.
[15] A. Maleki, Tetrahedron 68 (2012) 7827-
7833.
[16] V. Polshettiwar, R.S. Varma, Green Chem. 12 (2010) 743–754.
[17] X. Li, X.Y. Yan, H.H. Chang, L.C. Wang, Y. Zhang, W.W. Chen, Y. W. Li, W.L. Wei, Org. Biomol. Chem. 10 (2012) 495–497.
[18] D. Damodara, R. Arundhathi, P.R. Likhar, Adv. Synth. Catal. 356 (2014)189 –198.
[19] S. Banerjee, G. Sereda, Tetrahedron Lett. 50 (2009) 6959–6962.
[20] A. Javidan, A. Ziarati, J. Safaei-Ghomi, Ultrason. Sonochem. 21 (2014)1150–1154.
[21] I. C. Marcu, J. M. M. Millet, J. M. Herrmann, Catal. Lett. 78 (2002) 273-279.
[22] P. Gunasekaran, S. Perumal, P. Yogeeswari, D. Sriram, Eur. J. Med. Chem. 46 (2011) 4530-4536.
[23] A. Ziarati, J. Safaei-Ghomi, S. Rohani, Ultrason. Sonochem. 20 (2013) 1069–1075.