TiO2/nanoclinoptilolite, a recyclable and high efficient heterogeneous nanocatalyst, for the synthesis of 2-amino-4H-chromene derivatives

Subject Areas : Iranian Journal of Catalysis

Farzad Javadi ¹ , Reza Tayebee ²

1 - Department of Chemistry, School of Sciences, Hakim Sabzevari University, Sabzevar, 96179-76487, Iran.
2 - Department of Chemistry, School of Sciences, Hakim Sabzevari University, Sabzevar, 96179-76487, Iran.

Received: 2017-05-07 Accepted : 2017-08-26 Published : 2017-12-01

Keywords:

References:

[1] L. Edjlali, R.H. Khanamiri, Monatsh. Chem. (2016) 1-5.
[2] S.M. George, Chem. Rev. 95 (1995) 475-476.
[3] M.G. Dekamin, M. Eslami, A. Maleki, Tetrahedron 69 (2013) 1074-1085.
[4] S. Gao, C.H. Tsai, C. Tseng, C.-F. Yao, Tetrahedron 64 (2008) 9143-9149.
[5] I. Devi, P.J. Bhuyan, Tetrahedron Lett. 45 (2004) 8625-8627.
[6] A.M. Shestopalov, Y.M. Emeliyanova, A.A. Shestopalov, L.A. Rodinovskaya, Z.I. Niazimbetova, D.H. Evans, Org. Lett. 4 (2002) 423-425.
[7] M.C. Bagley, J.W. Dale, J. Bower, Chem. Commun. (2002) 1682-1683.
[8] F. Javadi, R. Tayebee, Microporous Mesoporous Mater. 231 (2016) 100-109.
[9] Y. Sarrafi, E. Mehrasbi, A. Vahid, M. Tajbakhsh, Chin. J. Catal. 33 (2012) 1486-1494.
[10] V.M. Joshi, R.L. Magar, P.B. Throat, S.U. Tekale, B.R. Patil, M.P. Kale, R.P. Pawar, Chin. Chem. Lett. 25 (2014) 455-458.
[11] S.S. Katkar, M.K. Lande, B.R. Arbad, S.T. Gaikwad, Chin. J. Chem. 29 (2011) 199-202.
[12] A.S. Waghmare, S.S. Pandit, Iran. Chem. Commun. 3 (2015) 291-301.
[13] S. Khaksar, A. Rouhollahpour, M. Saeed, J. Fluorine Chem. 141 (2012) 11.
[14] J.-C. Xu, W.-M. Li, H. Zheng, Y.-F. Lai, P.-F. Zhang, Tetrahedron 67 (2011) 9582-9587.
[15] R.J. Kalbasi, N. Mosaddegh, Catal. Commun. 12 (2011) 1231-1237.
[16] M.N. Elinson, A.I. Ilovaisky, V.M. Merkulova, P.A. Belyakov, A.O. Chizhov, G.I. Nikishin, Tetrahedron 66 (2010) 4043-4048.
[17] S. Tu, H. Jiang, Q. Zhuang, C. Miao, D. Shi, X. Wang, Y. Gao, Chin. J .Org. Chem. 23 (2003) 488-490.
[18] T.-S. Jin, A.-Q. Wang, F. Shi, L.-S. Han, L.-B. Liu, T.-S. Li, Arkivoc 14 (2006) 78-86.
[19] W.-B. Sun, P. Zhang, J. Fan, S.-H. Chen, Z.-H. Zhang, Synth. Commun. 40 (2010) 587-594.
[20] M.R. Naimi-Jamal, S. Mashkouri, A. Sharifi, Mol. Diversity 14 (2010) 473-477.
[21] S. Balalaie, M. Bararjanian, M.S. Ahmadi, S. Hekmat, P. Salehi, Synth. Commun. 37 (2007) 1097-1108.
[22] M. Seifi, H. Sheibani, Catal. Lett. 126 (2008) 275-279.
[23] J.M. Khurana, S. Kumar, Tetrahedron Lett. 50 (2009) 4125-4127.
[24] J.T. Li, W.Z. Xu, L.C. Yang, T.S. Li, Synth. Commun. 34 (2004) 4565-4571.
[25] R. Hekmatshoar, S. Majedi, K. Bakhtiari, Catal. Commun. 9 (2008) 307-310.
[26] M.M. Heravi, B.A. Jani, F. Derikvand, F.F. Bamoharram, H.A. Oskooie, Catal. Commun. 10 (2008) 272-275.
[27] B.S. Kumar, N. Srinivasulu, R. Udupi, B. Rajitha, Y.T. Reddy, P.N. Reddy, P. Kumar, J. Heterocycl. Chem. 43 (2006) 1691-1693.
[28] G. Sabitha, K. Arundhathi, K. Sudhakar, B. Sastry, J. Yadav, Synth. Commun. 39 (2009) 433-442.
[29] D. Fang, H.B. Zhang, Z.L. Liu, J. Heterocycl. Chem. 47 (2010) 63-67.
[30] S. Makone, S. Mahurkar, Green Sustainable Chem. 3 (2013) 27-32.
[31] M. Bahrami, A. Nezamzadeh-Ejhieh, Mater. Sci. Semicond. Process. 30 (2015) 275-284.
[32] N. Rajic, D. Stojakovic, N. Daneu, A. Recnik, J. Phys. Chem. Solids 72 (2011) 800-803.
[33] A. Godelitsas, T. Armbruster, Microporous Mesoporous Mater. 61 (2003) 3-24.
[34] M. Dalconi, A. Alberti, G. Cruciani, P. Ciambelli, E. Fonda, Microporous Mesoporous Mater. 62 (2003) 191-200.
[35] R. Tayebee, F. Javadi, G. Argi, J. Mol. Catal. A: Chem. 368 (2013) 16-23.
[36] D.W. Breck, Zeolite Molecular Sieves, John Wiley & Sons, New York, 1974.
[37] D. Kallo, J. Papp, J. Valyon, Zeolites 2 (1982) 13-16.
[38] M.M. Treacy, J.B. Higgins, Collection of Simulated XRD Powder Patterns for Zeolites, Elsevier, 2007.
[39] K. Thamaphat, P. Limsuwan, B. Ngotawornchai, Kasetsart J. Nat. Sci. 42 (2008) 357-361.
[40] Y. Ren, F. Zhang, W. Hua, Y. Yue, Z. Gao, Catal. Today 148 (2009) 316-322.
[41] F. Iacomi, Surf. Sci. 532 (2003) 816-821.
[42] A. Pourtaheri, A. Nezamzadeh-Ejhieh, Spectrochim. Acta Mol. Biomol. Spectrosc. 137 (2015) 338-344.
[43] J. Farzad, R. Tayebee, B. Bahramian, Appl Organometal Chem. (2017) doi: 10.1002/aoc.3779.
[44] A. Nezamzadeh-Ejhieh, F. Khodabakhshi-Chermahini, Ind. Eng. Chem. Res. 20 (2014) 695-704.
[45] S. Nemouchi, R. Boulcina, B. Carboni, A. Debache, C.R. Chim. 15 (2012) 394-397.
[46] L.-M. Wang, J.-H. Shao, H. Tian, Y.-H. Wang, B. Liu, J. Fluorine Chem. 127 (2006) 97-100.
[47] D. Shi, J. Mou, Q. Zhuang, X. Wang, J. Chem. Res. 2004 (2004) 821-823.
[48] K. Niknam, N. Borazjani, R. Rashidian, A. Jamali, Chin. J. Catal. 34 (2013) 2245-2254.
[49] M. Makvandi, F.A. Dil, A. Malekzadeh, M. Baghernejad, K. Niknam, Iran. J. Catal. 3 (2013) 221-228.