Brønsted acidic ionic liquid ([BMIm]HSO4) as an efficient catalysts for the one-pot synthesis of 2H-indazolo[2,1-b]phthalazine-trione derivatives
Subject Areas : Iranian Journal of CatalysisEsmayeel Abbaspour-Gilandeh 1 , Seyyedeh Cobra Azimi 2
1 - Young Researchers and Elites Club, Ardabil Branch, Islamic Azad University, Ardabil, Iran.
2 - Young Researchers and Elites Club, Rasht Branch, Islamic Azad University, Rasht, Iran.
Keywords:
Abstract :
[1] H. Valizadeh, A. Shockravi, Synth. Commun. 39 (2009) 4341-4349.
[2] H. Zang, M. Wang, B.W. Cheng, J. Song, Ultrason. Sonochem. 16 (2009) 301-303.
[3] T. Welton, Chem. Rev. 99 (1999) 2071-2084.
[4] P. Wasserscheid, W. Keim. Angew. Chem. Int. Ed. 39 (2000) 3772-3789.
[5] J. Dupont, R.F. Souza, P.A.Z. Suarez, Chem. Rev. 19 (2002) 3667-3692.
[6] T.L. Greaves, C.J. Drummond, Chem. Rev. 108 (2008) 206-237.
[7] J.A. Whitehead, G.A. Lawrance, A. McCluskey, Green Chem. 6 (2004) 313-315.
[8] B.S. Suryakant, F.S. Kiran, R.M. Balaji, B.S. Bapurao, S.S. Murlidhar. Bull. Korean Chem. Soc. 30 (2009) 2887-2889.
[9] S. Jasvinder, G. Neeraj, L.K. Goverdhan, Syn. Commun. 36 (2006) 2893-2900.
[10] S. Neeraj-Gupta, L.K. Goverdhan, S. Jasvinder. Catal. Commun. 8 (2007) 1323-1328.
[11] D. Zhao, Y. Liao, Z. Zhang, Clean 35 (2007) 42-48.
[12] E.C. Franklin, F.W. Bergstrom, Chem. Rev. 16 (1935) 305-361
[13] F.W. Bergstrom, Chem. Rev. 35 (1944) 77-277.
[14] F.W. Lichtenthaler, Acc. Chem. Res. 35 (2002) 728-737.
[15] V.11P. Litvinov, Russ. Chem. Rev. 72 (2003) 69-85.
[16] Y. Xu, Q.X. Guo, Heterocycles 63 (2004) 903-974.
[17] S. Grasso, G. De-Sarro, N. Micale, M. Zappala, G. Puia, M. Baraldi, C. De-micheli, J. Med. Chem. 43 (2000) 2851-2859.
[18] Y. Nomoto, H. Obase, H. Takai, M. Teranishi, J. Nakamura, K. Kubo, Chem. Pharm. Bull. 38 (1990) 2179-2182.
[19] N. Watanabe, Y. Kabasawa, Y. Takase, M. Matsukura, K. Miyazaki, H. Ishihara, K. Kodama, H. Adachi, J. Med. Chem. 14 (1998) 3367-3372.
[20] M. Sayyafi, M. Sayyedhamzeh, H.R. Khavasi, A. Bazgir, Tetrahedron 64 (2008) 2375-2378.
[21] J.M. Khurana, D. Magoo, Tetrahedron Lett. 50 (2009) 7300-7303.
[22] G. Shukla, R.K. Verma, G.K. Verma, M.S. Singh, Tetrahedron Lett. 52 (2011) 7195-7198.
[23] M. Kidwai, A. Jahan, R. Chauhan, N.K. Mishra, Tetrahedron Lett. 53 (2012) 1728-1731.
[24] R. Fazaeli, H. Aliyan, N. Fazaeli, Open Catal. J. 3 (2010) 14-18.
[25] E. Mosaddegh, A. Hassankhani, Tetrahedron Lett. 52 (2011) 488-490.
[26] M. Kidwai, R. Chauhan, A. Jahan, Chin. Sci. Bull. 57 (2012) 2273-2279.
[27] M.V. Reddy, G.C.S. Reddy, Y.T. Jeong, Tetrahedron 68 (2012) 6820-6828.
[28] R.G. Vaghei, R.K. Nami, Z.T. Semiromi, M. Amiri, M. Ghavidel, Tetrahedron 67 (2011) 1930-1937.
[29] L. Nagarapu, R. Bantu, H.B. Mereyala, J. Heterocycl. Chem. 46 (2009) 728-731.
[30] H.R. Shaterian, M. Ghashang, M. Feyzi, Appl. Catal. A: Gen. 345 (2008) 128-133.
[31] G. Sabitha, C. Srinivas, A. Raghavendar, J. S. Yadav, Helv. Chim. Acta 93 (2010) 1375-1380.
[32] M. Shekouhy, A. Hasaninejad, Ultrason. Sonochem. 19 (2012) 307–313.
[33] A. Hasaninejed, M.R. Kazerooni, A. Zare, Catal. Today 196 (2012) 148-155.
[34] E. Abbaspour-Gilandeh, S.C. Azimi, K. Rad-Moghadam, A. Mohammadi-Barkchai, Iran. J. Catal. 2 (2013) 91-97.
[35] E. Abbaspour-Gilandeh, S.C. Azimi, K. Rad-Moghadam, A. Mohammadi-Barkchai, Iran. J. Catal. 1 (2013) 15-20.
[36] K. Rad-Moghadam, S.C. Azimi, E. Abbaspour-Gilandeh, Tetrahedron Lett. 54 (2013) 4633-4636.
[37] F. Al-Assar, K.N. Zelenin, E.E. Lesiovskaya, I.P. Bezhan, B.A. Chakchir, Pharm. Chem. J. 36 (2002) 598-603.
[38] M. Saha, S. Phukan, R. Jamatia, S. Mitra, A.K. Pal, RSC Adv. 3 (2013) 1714–1721.
[39] H.R. Shaterian, A. Hosseinian, M. Ghashang, Arkivoc. ii (2009) 59-67.
[40] J. Fraga-Dubreuil, K. Bourahla, M. Rahmouni, J.P. Bazureau, J. Hamelin, Catal. Commun. 3 (2002) 185-190.