Fe(HSO4)3/SiO2: An efficient and heterogeneous catalyst for cyclization of 2- aminochalcones to 2- aryl-2,3- dihydroquinolin- 4(1H)- ones
Subject Areas : Iranian Journal of CatalysisHossein Eshghi 1 , Mohammad Rahimizadeh 2 , Seyed Mohsen Mousavi 3
1 - Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad, Mashhad 91775-1436, Iran.
2 - Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad, Mashhad 91775-1436, Iran.
3 - Department of Chemistry, School of Sciences, Ferdowsi University of Mashhad, Mashhad 91775-1436, Iran.
Keywords:
Abstract :
[1] R. Pingaew, A. Saekee, P. Mandi, C. Nantasenamat, S. Prachayasittikul, S. Ruchirawat, V. Prachayasittikul, Europ. J. Med. Chem. 85 (2014) 65-76.
[2] A. Pejović, I. Damljanović, D. Stevanović, M. Vukićević, S.B. Novaković, G.A. Bogdanović, N. Radulović, R.D. Vukićević, Polyhedron 31 (2012) 789-795.
[3] A.L. Tokes, G. Litkei, Synth. Commun. 23 (1993) 895-902.
[4] N. Ahmed, J.E. van Lier, Tetrahedron Lett. 48 (2007) 13-15.
[5] R. Abonia, P. Cuervo, J. Castillo, B. Insuasty, J. Quiroga, M. Nogueras, J. Cobo, Tetrahedron Lett. 49 (2008) 5028-5031.
[6] N. Ahmed, J.E. van Lier, Tetrahedron Lett. 47 (2006) 2725-2729.
[7] M. Chelghoum, M. Bahnous, A. Bouraiou, S. Bouacida, A. Belfaitah, Tetrahedron Lett. 53 (2012) 4059-4061.
[8] D. Kumar, G. Patel, B.G. Mishra, R.S. Varma, Tetrahedron Lett. 49 (2008) 6974-6976.
[9] R. Sakirolla, M. Yaeghoobi, N.A. Rahman, Monatsh. Chem. 143 (2012) 797-800.
[10] K.C. Lekhok, D. Bhuyan, D. Prajapati, R.C. Boruah, Mol. Div. 14 (2010) 841-846.
[11] P. Kumar, D.N. Dhar, Synth. Commun. 25 (1995) 1933-1938.
[12] N. Ahmed, H. Kumar, B.V. Babu, Synth. Commun. 43 (2013) 567-581.
[13] R.N. Bhattacharya, P. Kundu, G. Maiti, Synth. Commun. 40 (2010) 476-481.
[14] V.K. Rao, M.S. Rao, A. Kumar, J. Het. Chem. 48 (2011) 1356-1360.
[15] H. Eshghi, M. Bakavoli, H. Moradi, Org. Prep. Proced. Int. 43 (2011) 302-307.
[16] H. Eshghi, S.M. Seyedi, E. Safaei, M. Vakili, A. Farhadipour, M. Bayat-Mokhtari, J. Mol. Cat. A: Chem. 363–364 (2012) 430-436.
[17] H. Eshghi, M. Rahimizadeh, M. Hosseini, A. Javadian-Saraf, Monatsh. Chem. 144 (2012) 197-203.
[18] H. Eshghi, M. Rahimizadeh, N. Attaran, M. Bakavoli, J. Iran. Chem. Soc. 10 (2013) 1151-1157.
[19] A. Khojastehnezhad, M. Rahimizadeh, H. Eshghi, F. Moeinpour, Chin. J. Cat. 35 (2014) 376-382.
[20] H. Eshghi, M. Rahimizadeh, S. Saberi, Catal. Commun. 9 (2008) 2460-2466.
[21] Y.M. Lin, Y. Zhou, M.T. Flavin, L.M. Zhou, W. Nie, F.C. Chen, Bioorg. Med. Chem. 10 (2002) 2795-2802.
[22] R.A. Bunce, B. Nammalwar, J. Het. Chem. 48 (2011) 613-619.
[23] U.P. Lad, M.A. Kulkarni, U.V. Desai, P.P. Wadgaonkar, C.R. Chim. 14 (2011) 1059-1064.
[24] L. Jianjun, J. Linyong, Y. Chuanming, S. Weike. J. Chem. Res. 33 (2009) 170-173.
[25] D. Kumar, G. Patel, A. Kumar, J. Het. Chem. 46 (2009) 791-795.
[26] H. Eshghi, M. Rahimizadeh, S.M. Mousavi, Nat. Prod. Res. 28 (2014) 438-443.