One-pot three component synthesis of 2-amino-4H-chromenes under green and high efficient conditions
Subject Areas : Iranian Journal of Catalysis
Leila Moradi
1
(Faculty of Chemistry, Department of Organic Chemistry, University of Kashan, P.O. Box 8731751167 Kashan, I. R. Iran.)
Mina Zare
2
(Faculty of Chemistry, Department of Organic Chemistry, University of Kashan, P.O. Box 87317-51167, Kashan, Iran.)
Keywords:
Abstract :
[1] B.C. Das, S. Mohapatra, P.D. Campbell, S. Nayak, S.M. Mahalingam, T. Evans, Tetrahedron Lett. 51 (2010) 2567-2570.
[2] H.R. Shaterian, M. Arman, F. Rigi, J. Mol. Liq. 158 (2011) 145-150.
[3] J.M. Khurana, B. Nand, P. Saluja, Tetrahedron. 66 (2010) 5637-5641.
[4] H. Nagabhushana, S.S. Saundalkar, L. Muralidhar, B.M. Nagabhushana, C.R. Girija, D. Nagaraja, M.A. Pasha, V.P. Jayashankara, Chin. Chem. Lett. 22 (2011) 143-146.
[5] L. Moafi, S. Ahadi, A. Bazgir, Tetrahedron Lett. 51 (2010) 6270-6274.
[6] B. Mohtat, H. Djahaniani, I. Yavari, M.G. Dehbalaei, S.A. Jam, Chin. Chem. Lett. 22 (2011) 771-773.
[7] O.M. Singh, N.S. Devi, D.S. Thokchom, G.J. Sharma, Eur. J. Med. Chem. 45 (2010) 2250-2257.
[8] S. Song, L. Song, B. Dai, H. Yi, G. Jin, S. Zhu, M. Shao, Tetrahedron 64 (2008) 5728-5735.
[9] Y. Gao, D.M. Du, Tetrahedron: Asymmetry 23 (2012) 1343-1349.
[10] B.V. Subba Reddy, M. Ramana Reddy, G. Narasimhulu, J.S. Yadav, Tetrahedron Lett. 51 (2010) 5677-5679.
[11] R. Maggi, R. Ballini, G. Sartori, R. Sartorio, Tetrahedron Lett. 45 (2004) 2297-2299.
[12] J.S. Yadav, B.V. Subba Reddy, S.K. Biswas, S. Sengupta, Tetrahedron Lett. 50 (2009) 5798-5801.
[13] H. Eshghi, M. Bakavoli, J. Abedini-Torghabeh, M. Rahimizadeh, Chin. Chem. Lett. 23 (2012) 1153-1156.
[14] K. Takenaka, S.C. mohanta, M.L. Patil, C.V. Laxman, S. Takizawa, T. Suzuki, H. Sasai, Org. Lett. 12 (2011) 3480-3483.
[15] Y. Liu, J. Qian, S. Lou, J. Zhu, Z. Xu, J. Org. Chem. 75 (2010) 1309-1312.
[16] D. Rajguru, B.S. Keshwal, S. Jain, Chin. Chem. Lett. 24 (2013) 1033-1036.
[17] H.J. Wang, J. Lu, Z.H. Zhang, Monatsh. Chem. 141 (2010) 1107-1112.
[18] N. Ramireddy, S. Abbaraju, C.G. Zhao, Tetrahedron Lett. 52 (2011) 6792-6295.
[19] R.Y. Guo, Z.M. An, L.P. Mo, S.T. Yang, H.X. Liu, S.X. Wang, Z.H. Zhang, Tetrahedron 69 (2013) 9931-9938.
[20] R.Y. Guo, Z.M. An, L.P. Mo, R.Z. Wang, H.X. Liu, S.X. Wang, Z.H. Zhang, ACS Comb. Sci. 15 (2013) 557–563.
[21] A.M. ElAgrody, A.M. AlDies, A.M. Fouda, Eur. J. Chem. 5 (2014) 133-137.
[22] C.B. Sangani, N.M. Shah, M.P. Patel, R.G. Patel, J. Serb. Chem. Soc. 77 (2012) 1165-1174.
[23] S. Makarem, A.A. Mohammadi, A.R. Fakhari, Tetrahedron Lett. 49 (2008) 7194-7196.
[24] D.S Raghuvanshi, K.N Singh. Arkivoc (2010) 305-317.
[25] S. Khaksar, A. Rouhollahpour, S.M. Talesh, J. Fluorine Chem. 141 (2012) 11–15.
[26] M. Kidwai, Pure. Appl. Chem. 73 (2001) 147-151.
[27] R.L. Magara, P.B. Thorata, V.B. Jadhava, S.U. Tekalea, S.A. Dakea, B.R. Patil b, R.P. Pawara, J. Mol. Catal. A: Chem. 374–375 (2013) 118–124.
[28] A.M. El-Maghraby, Org. Chem. Int. (2014) Article ID 715091, 6 pp.
[29] M. Mirza-Aghayan, S. Nazmdeh, R. Boukherroub, M. Rahimifard, A.A. Tarlani, M. Abolghasemi-Malakshah, Synth. Commun. 43 (2013) 1499–1507.
[30] Z. Zhou, F. Yang, L. Wu, A. Zhang, Chem. Sci. Trans. 1 (2012) 57-60
[31] J. Albadi, A. Mansournezhad, M. Darvishi-Paduk. Chin. Chem. Lett. 24 (2013) 208–210.
[32] D. Kumar, V.B. Reddy, B.G. Mishra, R.K. Rana, M.N. Nadagoudac, R.S. Varma, Tetrahedron. 63 (2007) 3093-3097.
[33] S.R. Kale, S.S. Kahandal, A.S. Burange, M.B. Gawande, R.V. Jayaram, Catal. Sci. Technol. 3 (2013) 2050-2056.
[34] J. Safari, M. Heydarian, Z. Zarnegar, Arab. J. Chem. 27 (2013) 1878-1882.
[35] T.S. Jin, J.C. Xiao, S.J. Wang, T.S. Li, Ultrason. Sonochem. 11 (2004) 393-397.
[36] X.S. Wang, G.S. Yanga, G. Zhao, Tetrahedron 19 (2008) 709-711.
