One-pot synthesis of 2,4,5-trisubstituted imidazoles catalyzed by dicationic magnetic room temperature ionic liquid

Subject Areas : Iranian Journal of Catalysis

Bijan Mombani Godajdar ¹ , Ali Reza Kiasat ²

1 - Department of Chemistry, Omidiyeh Branch, Islamic Azad University, Omidiyeh, Iran.
2 - Department of Chemistry, College of Science, Shahid Chamran University, Ahwaz, Iran.

Received: 2013-09-13 Accepted : 2013-12-15 Published : 2013-12-01

Keywords:

References:

[1] S. Hayashi, H. Hamagachi, Chem. Lett., 33 (2004) 1590-1591.
[2] S. Lee, S. Ha, H. Jin, C. You, Y. Koo, J. Appl. Phys., 101 (2007) 09J102-3.
[3] M. Okuno, H. O. Hamaguchi, S. Hayashi, Appl. Phys. Lett., 89 (2006) 132506:1–132506:2.
[4] S.H. Lee, S.H. Ha, S.S. Ha, H.B. Jin, C.Y. You, Y.M. Koo, J. Appl. Phys., 101 (2007) 09J102:1–09J102:3.
[5] S.H. Lee, S.H. Ha, C.Y. You, Y.M. Koo, Korean J. Chem. Eng., 24 (2007) 436–437.
[6] Y. Yoshida, G. Saito, J. Mater. Chem., 16 (2006) 1254–1262.
[7] R.E. Del Sesto, T.M. McCleskey, A.K. Burrell, G.A. Baker, J.D. Thompson, B.L. Scott, J.S. Wilkes, P. Williams, Chem. Commun., 4 (2008) 447–449.
[8] B. Mallick, B. Balke, C. Felser, A.V. Mudring, Angew. Chem. Int. Ed., 47 (2008) 7635–7638.
[9] J. Wang, H. Yao, Y. Nie, X. Zhang, J. Li, J. Mol. Liq., 169 (2012) 152-155.
[10] D.N. Sushma, K. Nitin, M. Siddeswaran, Indian J. Hetero. Chem., 15 (2005) 91-92.
[11] P. Cozzi, G. Carganico, D. Fusar, M. Grossoni, M. Menichincheri, V. Pinciroli, R. Tonani, F. Vaghi, P. Salvati, J. Med. Chem., 36 (1993) 2964-2972.
[12] M. Harfenist, E.F. Soroko, G.M. Mekenzie, J. Med. Chem., 21 (1978) 405-409.
[13] L.C. Patricia, M.G. Christine, B.M. Stephen, J. Agric. Food Chem., 36 (1988) 1076-1079.
[14] H. Miyachi, H. Kiyota, M. Segawa, Chem. Lett., 18 (1998) 2163-2168.
[15] M. Shen, C. Cai, W. Yi, J. Fluorine Chem., 129 (2008) 541-544.
[16] G.V. M. Sharma, Y. Jyothi, P. Sree Lakshmi, Synth. Commun., 36 (2006) 2991-3000.
[17] M.M. Heravi, K. Bakhtiari, H.A. Oskooie, S. Taheri, J. Mol. Catal. A: Chem., 263 (2007) 279-281.
[18] A. Shaabani, A. Rahmati, E. Farhangi, Z. Badri, Catal. Commun., 8 (2007) 1149-1152.
[19] H. Zang, Q. Su, Y. Mo, B.W. Cheng, S. Jun, Ultrason. Sonochem., 17 (2010) 749–751
[20] M. Xia, Y. Lu, J. Mol. Catal. A: Chem., 265 (2007) 205–208
[21] S.A. Siddiqui, U.C. Narkhede, S.S. Palimkar, T. Daniel, R.J. Lahoti, K.V. Srinivasan, Tetrahedron, 61 (2005) 3539–3546
[22] X. Liu, M. Lu, Y. Wang, Chiang Mai J. Sci., 38 (2011) 601-607.
[23] S.D. Jadhave, N.D. Kokare, S.D. Jadhave, J. Hetero. Chem., 45 (2009) 1461-1464.
[24] B.M. Godajdar, A.R. Kiasat, M.M. Hashemi, J. Mol. Liq., 183 (2013) 14-19.
[25] B.M. Godajdar, A.R. Kiasat, M.M. Hashemi, Heterocycles, 87 (2013) 559-570.
[26] Y. Yoshida, G. Saito, J. Mater. Chem., 16 (2006) 1254-1262.
[27] S.D. Sharma, P. Hazarika, D. Konwar, Tetrahedron Lett., 49 (2008) 2216-2220.
[28] R.S. Joshi, P.G. Mandhane, M.U. Shaikh, R.P. Kale, C.H. Gill, Chin. Chem. Lett., 21 (2010) 429-432.
[29] R. Khosropour, Ultrason. Sonochem., 15 (2008) 659-664.
[30] S. Samai, G.C. Nandi, p. Singh, M.S. Singh, Tetrahedron, 65 (2009) 10155-10161.
[31] M.M. Khodaei, K. Bahrami, I. Kavianinia, J. Chin. Chem. Soc., 54 (2007) 829-833.
[32] A. Mohammadi, H. Keshvari, R. Sandaroos, H. Rouhi, J. Chem. Sci., 124 (2012) 717–722.
[33] J.N. Sangshetti, N.D. Kokare, S.A. Kothakar, D.B. Shinde, Mont. Fur. Chem., 139 (2008) 125-127.