CuO-CeO2 nanocomposite: A green recyclable catalyst for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones

Albadi, Jalal; Mansournezhad, Azam

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	CuO-CeO2 nanocomposite: A green recyclable catalyst for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones
Article 3, Volume 3, Issue 2, Spring 2013, Page 73-77 PDF (396.91 K)
Authors
Jalal Albadi ¹; Azam Mansournezhad²
¹College of Science, Behbahan Khatam Alanbia University of Technologhy, Behbahan, Iran.
²Department of Chemistry, Gachsaran Branch, Islamic Azad University, Gachsaran, Iran.
Abstract
CuO-CeO2 nanocomposite is reported as a green and highly efficient recyclable catalyst for the multicomponent synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones under solvent-free conditions. The catalyst was synthesized by co-precipitation method and characterized by XRD, BET specific surface area, FESEM and EDS analysis.
Keywords
CuO-CeO2 nanocomposite; Biginelli reaction; Solvent-free conditions; 3; 4-dihydropyrimidin-2(1H)-ones/thiones


References
[1] K.S. Atwal, B.N. Swanson, S.E. Unger, D.M. Floyd, S. Moreland, A. Hedberg, B.C. O’Reilly, J. Med. Chem. 34 (1991) 806-811. [2] P. Biginelli, Gazz. Chim. Ital. 23 (1893) 360-413. [3] A. Bamoniri, B.F. Mirjalili, S. Nazemian, Iran. J. Catal. 2 (2012) 17-21. [4] K.K. Pasunooti, H. Chai, C.N. Jensen, B.K. Gorityala, S. Wang, X.-W. Liu, Tetrahedron Lett. 52 (2011) 80-84. [5] Z. Fang, Y. Lam, Tetrahedron Lett. 67 (2011) 1294-1297. [6] M. Zeinali-Dastmalbaf, A. Davoodnia, M.M. Heravi, N. Tavakoli-Hoseini, A. Khojastehnezhad, H.A. Zamani, Bull. Korean Chem. Soc. 32 (2011) 656-658. [7] O. Rosati, M. Curini, F. Montanari, M. Nocchetti, S. Genovese, Catal. Lett. 141 (2011) 850-853. [8] S.D. Salim, K.G. Akamanchi, Catal. Lett. 12 (2011) 1153-1156. [9] S. Asghari, M. Tajbakhsh, B. Jafarzadeh Kenari, S. Khaksar, Chin. Chem. Lett. 22 (2011) 127-130. [10] L. Khazdooz, A. Zarei, A. R. Hajipour, N. Sheikhan, Iran. J. Catal. 2 (2012) 173-178. [11] H. Sharghi, M. Jokar, Synth. Commun. 39 (2009) 958-979. [12] F. Shirini, M.A. Zolfigol, E. Mollarazi, Synth. Commun. 36 (2006) 2307-2310. [13] M.M. Heravi, K. Bakhtiari, F. Bamoharram, Catal. Commun. 7 (2006) 373-376. [14] K.K. Pasunooti, H. Chai, J. Chantel Nixon, G. Bala Kishan, W. Siming, L. Xue-Wei, Tetrahedron Lett. 52 (2011) 80-84. [15] G.B. Dharma Rao, B.N. Acharya, S.K. Verma, M.P. Kaushik, Tetrahedron Lett. 52 (2011) 809-812. [16] M.A. Bigdeli, G. Golami, E. Sheikhhosseini, Chin. Chem. Lett. 22 (2011) 903-906. [17] Q. Liu, N. Pan, J. Xu, W. Zhang, F. Kong, Synth. Commun. 43 (2013) 139-146. [18] M. Mirzai, H. Valizadeh, Synth. Commun. 42 (2012) 1268-1277. [19] N.D. Abhishek, K.P. Vaibhav, K.R. Dipak, J. Chem. Sci. 124 (2012) 921-926. [20] H. Sharghi, M. Hosseini, Synthesis. (2002)1057-1059. [21] S. M. Hosseini, H. Sharghi, J. Org. Chem. 69 (2004) 6953-6956. [22] S.F. Yin, B.Q. Xu, S.J. Wang, C.F. Ng, C.T. Au, Catal. Lett. 96 (2004) 113-116 [23] M.T. Drexler, M.D. Amiridis, Catal. Lett. 79 (2002) 175-181. [24] R.S. Varma, Green. Chem. 1 (1999) 43-55. [25] S. Samantaray, D.K. Pradhan, G. Hota, B.G. Mishra, Chem. Eng. J. 193 (2012) 1-9. [26] S.Li, W. Zhang, M.H. So, C.M. Che, R. Wang, R. Chen, J. Mol. Catal. A: Chem. 359 (2012) 81-87. [27] A. Razeghi, A. Khodadadi, H. Ziaie-Azad, Y. Mortazavi, Chem. Eng. J. 164 (2010) 214-220. [28] J. Albadi, A. Razeghi, A. Mansournezhad, H. Abbaszadeh, J. Nanoparticles 9 (2013) 83-889. [29] J. Albadi, M. Keshavarz, M. Abedini, M. Vafaie-nezhad, Chin. Chem. Lett. 23 (2012) 797-800. [30] J. Albadi, M. Keshavarz, F. Shirini, M. Vafaie-nezhad, Catal. Commun. 27 (2012) 17-20. [31] J. Albadi, N. Iravani, M. Khoshakhlagh, Iran. J. Catal. 2 (2012) 85-89. [32] J. Albadi, N. Iravani, F. Shirini, F. Dehghan, J. Chem. Res. (2012) 610-611. [33] F. Shirini, M. A. Zolfigol, J. Albadi, Chin. Chem. Lett. 22 (2011) 318-321. [34]. J. Albadi, A. Mansournezhad, M. Baghernezhad, N. Frozan, 57 (2013) 169-171.
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