New method for preparation of MWCNT-SO3H as an efficient and reusable catalyst for the solvent-free synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones
Subject Areas : Iranian Journal of CatalysisLeila Moradi 1 , Gholam Reza Najafi 2 , Hakimeh Saeidiroshan 3
1 - Faculty of Chemistry, Department of Organic Chemistry, University of Kashan, P.O. Box 8731751167 Kashan, I. R. Iran.
2 - Department of Organic Chemistry, Islamic Azad University of Qom, Iran.
3 - Department of Organic Chemistry, Islamic Azad University of Qom, Iran.
Keywords:
Abstract :
[1] P.M. Ajayan, Chem. Rev. 99 (1999) 1787-1800.
[2] S. Iijima, Nature 354 (1999) 56-58.
[3] T.W. Ebbesen, H.J. Lezec, H. Hiura, J.W. Bennett, H.F. Ghaemi, T. Thio, Nature 382 (1996) 54-56.
[4] N.H. Thai, M.K. Yeh, J.H. Liu, Carbon 42 (2004) 2774-2777.
[5] Z.H. Gan, Q.Zhao, Zh. N. Gu, Q.K. Zhuang, Anal. Chim. Acta 511 (2004) 239-247.
[6] R.H. Baughman, A.A. Zakhidov, W.A. Heer, Science 297 (2002) 787-792.
[7] A.C. Dillon, K.M. Jones, T.A. Bekkedahl, C.H. Kiang, D.S. Bethune, M.J. Heben, Nature 386 (1997) 377-379.
[8] E. Steen, F.F. Prinsloo, Catal. Today 71 (2002) 327-
334.
[9] M. Salavati-Niasari, E. Esmaeili, H. Seyghalkar, M. Bazarganipour, Inorg. Chim. Acta 375 (2011) 11-19.
[10] M. Penza, F. Antolini, M.V. Antisari, Sens. Actuators B 100 (2004) 47-59.
[11] G.S. Choi, K.H. Son, D.J. Kim, Microelect. Eng. 66 (2003) 206-212.
[12] L.Q. Jiang, L. Gao, Carbon 41 (2003) 2923-2929.
[13] N. Karousis, N. Tagmatarchis, D. Tasis, Chem. Rev. 110 (2011) 5366-5397.
[14] Z. Li, Y.Q. Dong, M. Haussler, J.W.Y. Lam, Y.P. Dong, L.J. Wu, K.S. Wong, B.Z. Tang, J. Phys. Chem. B 110 (2006) 2302-2309.
[15] W.Z. Yuan, Y. Mao, H. Zhao, J.Z. Sun, H.P. Xu, J.K. Jin, Q. Zheng, B.Z. Tang, Macromolecules 41 (2008) 701-707.
[16] X. Peng, S.S. Wong, Adv. Mater. 21 (2009) 625-
642.
[17] F. Liang, J.M. Beach, P.K. Rai, W. Guo, R.H. Hauge, M. Pasquali, R.E. Smalley, W.E. Billups, Chem. Mater. 18 (2006) 1520-1524.
[18] Z. Zarnegar, J. Safari, J. Nanopart. Res. 16 (2014) 2509-2523
[19] P. Wasserscheid, W. Keim, Angew. Chem. Int. Ed. 39 (2000) 3772-3789.
[20] R. Sheldon, Chem. Comm. (2001) 2399-2407.
[21] C.M. Gordon, Appl. Catal. A 222 (2001) 101-117.
[22] C.O. Kappe, Acc. Chem. Res. 33 (2000) 879-888.
[23] C.O. Kappe, Eur. J. Med. Chem. 35 (2000) 1043-1052.
[24] U.M. Lindstrom, Chem. Rev. 102 (2000) 2751-2572.
[25] (a) J.C. Legeay, J.J.V. Eynde, J.P. Bazureau, Tetrahedron Lett. 48 (2007) 1063-1068. (b) B. Desai, D. Dallin-ger, C.O. Kappe, Tetrahedron. 62 (2006) 4651-4664.
[26] P.G. Mandhane, R.S. Joshi, D.R. Nagargoje. C.H. Gill, Tetrahedron Lett. 51 (2010) 3138-3140.
[27] M.S. Manhas, S.N. Ganguly, S. Mukherjee, A.K. Jain, A.K. Bose, Tetrahedron Lett. 47 (2006) 2423-2425.
[28] K.K. Kapoor, B.A. Ganai, S. Kumar, C.S. Andotra, Can. J. Chem. 84 (2006) 433-437.
[29] A. Dondoni, A. Massi, Tetrahedron Lett. 42 (2001) 7975-7978.
[30] V.R. Rani, N. Srinivas, M.R. Kishan, S.J. Kulkarni, K.V. Raghavan, Green. Chem. 3 (2001) 305-307.
[31] P. Salehi, M. Dabiri, M.A. Zolfigol, M.A. Fard, Tetrahedron Lett. 44 (2003) 2889-2892.
[32] J.C. Bussolari, P.A. McDonnell, J. Org. Chem. 65 (2000) 6777-6779.
[33] G. Maiti, P. Kundu, C. Guin, Tetrahedron Lett. 44 (2003) 2757-2758.
[34] A. Shaabani, A. Bazgir, F. Teimouri, Tetrahedron Lett. 44 (2003) 857-859.
[35] H. Salehi, Q.X. Guo, Synth. Commun. 34 (2004)171-179.
[36] W. Li, Y. Bai, Y.K .Zhang, M.L. Sun, R.M. Cheng, X.C. Xu, Y.Chen, Y. Mo, Synth. Met. 155 (2005) 509-515.
[37] R. Fareghi-Alamdari, M. Golestanzadeh, F. Agend, N. Zekri, J. Chem. Sci. 125 (2013) 1185–1195.
[38] E. Smith, G. Dent, Modern Raman spectroscopy: A practical approach. Wiley & Sons, 2005, 135-140.
[39] R.E. Barletta, B.N. Gros, M.P. Herring, J. Raman Spectrosc. 40 (2009) 972–981
[40] Y. Yu, D. Liu, C. Liu, G. Luo, Bioorg. Med. Chem. Lett. 17 (2007) 3508-3510.
[41] H. Khabazzadeh, K. Saidi, H. Sheibani, Bioorg. Med. Chem. Lett. 18 (2008) 278-280.
[42] A.K. Bose, M.S. Manhas, S. Pednekar, S.N. Ganguly, H. Dang, W. He, A. Mandadi, Tetrahedron Lett. 46 (2005) 1901-1903.
[43] C.O. Kappe, D. Kumar, R.S. Verma, Synthesis (1999) 1799-1803.
[44] B.C. Ranu, A. Hajra, U. Jana, J. Org. Chem. 65 (2000) 6270-6272.
[45] A. Debache, R. Boulcina, R. Tafer, A. Belfaitah, S. Rhouati, B. Carboni, Chin. J. Chem. 26 (2008) 2112-2116.
[46] S. Besoluk, M. Kucukislamoglu, M. Nebioglu, M. Zengin, M. Arslan, J. Iran. Chem. Soc. 5 (2008) 62-66.
[47] A.V. Narsaiah, B.K. Nagaiah, Synthesis (2004) 1253-1266.
[48] K.A. Kumar, M. Kasthuraiah, C.S. Reddy, D. Reddy, Tetrahedron Lett. 42 (2001) 7873-2875.
[49] G.L. Zhang, H.X. Cai, Synth. Commun. 35 (2005) 829-833.
[50] G. Maiti, P. Kundu, C. Guin, Tetrahedron Lett. 44 (2003) 2757-2768.
[51] B.P. Bandgar, V.T. Kamble, S.N. Bavikar, Abasaheb Dhavane, J. Chinese Chem. Soc. 54 (2007) 263-266.
[52] D.L. da Silva, S.A. Fernandes, A.A. Sabino, A. de Fatima, Tetrahedron Lett. 52 (2011) 6328-6330.
[53] S.R. Jetti, N. Babu, P. Paliwal, A. Bhatewra, T. Kadre, S. Jain, Der. Pharm. Chem. 4 (2012) 417-427
[54] B.J. Khairnar, R.J. Kapade, K.M. Borse, B.R. Chaudhari, Orient. J. Chem. 26 (2010) 655-660.