Li(OHCH2CH2NH2)(CF3OAC): A novel and homogeneous acidic ionic liquid catalyst for efficient synthesis of 2-amino-4H-chromene derivatives
Subject Areas : Iranian Journal of CatalysisEsmayeel Abbaspour-Gilandeh 1 , Seyyedeh Cobra Azimi 2
1 - Young Researchers and Elites Club, Ardabil Branch, Islamic Azad University, Ardabil, Iran.
2 - Young Researchers and Elites Club, Rasht Branch, Islamic Azad University, Rasht, Iran.
Keywords:
Abstract :
[1] A.S.H. Salem, H.S. Hamid, Chem. Eng. Technol. 20 (1997) 342-347.
[2] P. Wasserscheid, W. Keim, Angew. Chem. Int. Ed. 39 (2000) 3772-3789.
[3] T. Welton, Chem. Rev. 248 (2004) 2459-2477.
[4] P.T. Anastas, J.C. Warner, Green Chemistry: Theory and Practice, Oxford University Press, New York, 1998, p. 30.
[5] S.T. Handy, Chem. Eur. J. 9 (2003) 2938-2944.
[6] P. Luis, A. Garea, A.J. Irabien, J. Membr. Sci. 330 (2009) 80-89.
[7] C. Hardacre, J. Holbrey, M. Nieuwenhuyzen, T.G.A. Youngs, Acc. Chem. Res. 40 (2007) 1146-1155.
[8] V.I. Parvulescu, C. Hardacre, Chem. Rev. 107 (2007) 2615-2665.
[9] S.M.S. Chauhan, S. Agarwal, P. Kumari, Synth. Commun. 37 (2007) 2917-2925.
[10] Z. Dong, X. Liu, J. Feng, M. Wang, L. Lin, X. Feng, Eur. J. Org. Chem. 2011 (2011) 137-142.
[11] L. Bonsignore, G. Loy, D. Secci, A. Calignano, Eur. J. Med. Chem. 28 (1993) 517-520.
[12] A. Shaabani, S. Samadi, Z. Badri, A. Rahmati, Catal. Let. 104 (2005) 39-43.
[13] M. Khoobi, L. Ma’mani, F. Rezazadeh, Z. Zareie, A. Foroumadi, A. Ramazani, A. Shafiee, J. Mol. Catal. A: Chem. 359 (2012) 74-80.
[14] J.M. Khurana, S. Kumar, Tetrahedron Lett. 50 (2009) 4125-4127.
[15] H. Mehrabi, H. Abusaidi, J. Iran. Chem. Soc. 7 (2010) 890-894.
[16] M.J. Khurana, B. Nand, P. Saluja, Tetrahedron 66 (2010) 5637-5641.
[17] M.M. Heravi, B. Alimadadi, F. Derikvand, F.F. Bamoharram, H.A. Oskooie, Catal. Commun. 10 (2008) 272-275.
[18] S. Abdolmohammadi, S. Balalaie, Tetrahedron Lett. 48 (2007) 3299-3303.
[19] H.J. Wang, J. Lu, Z.H. Zhang, Monatsh. Chem. 141 (2010) 1107-1112.
[20] H. Mehrabi, M. Kazemi, Chin. Chem. Lett. 22 (2011) 1419-1422.
[21] K. Tabatabaeian, H. Heidari, M. Mamaghani, N.O. Mahmoodi, Appl. Organomet. Chem. 26 (2012) 56-61.
[22] K. Rad-Moghadam, S.C. Azimi, E. Abbaspour-Gilandeh, Tetrahedron Lett. 54 (2013) 4633-4636.
[23] E. Abbaspour-Gilandeh, S.C. Azimi, K. Rad-Moghadam, A. Mohammadi-Barkchai, Iran. J. Catal. 3 (2013) 15-20
[24] A. Shaabani, S. Samadi, Z. Badri, A. Rahmati, Catal. Lett. 104 (2005) 39-43.
[25] W. Xiang-Shan, Z. Zhao-Sen, S. Da-Qing, W. Xian-Yong, Z. Zhi-Min, Chin. J. Org. Chem. 25 (2005) 1138-1141.
[26] M. Seifi, H. Sheibani. Catal. Lett. 126 (2008) 275-279.
[27] S. Balalaie, M. Bararjanian, M. Sheikh-Ahmadi. Synth. Commun. 37 (2007) 1097-1108.
[28] L.M. Wang, J.H. Shao, H. Tian, Y.H. Wang, B. Liu. J. Fluorine Chem. 127 (2006) 97-100.
[29] T.S. Jin, A.Q. Wang, X. Wang, J.S. Zhang, T.S. Li. Synlett 5 (2004) 871-873.
[30] R. Hekmatshoar, S. Majedi, K. Bakhtiari. Catal. Commun. 9 (2008) 307-310.
[31] Y.A. Sharanin, A.M. Shestopalov. Zh. Org. Khim. 25 (1989) 1331-1335.
[32] J.-C. Xu, W.-M. Li, H. Zheng, L. Yi-Feng, P.-F. Zhang, Tetrahedron 67 (2011) 9582–9587.
[33] M. Hong, C. Cai, J. Chem. Res. 34 (2010) 568-570.
[34] S. Gowravaram, K. Arundhathi, K.B.S. Sudhakar, J.S. Yadav, Synth. Commun. 39 (2009) 433-442;
[35] M.J. Khurana, B. Nand, P. Saluja, Tetrahedron 66 (2010) 5637-5641.
[36] Y. Yi, G. Hongyun, L. Xiaojun, J. Heterocycl. Chem. 48 (2011) 1264-1268.
[37] A. Shaabani, R. Ghadari, S. Ghasemi, M. Pedarpour, A.H. Rezayan, A. Sarvary, S.W. Ng, J. Comb. Chem. 11 (2009) 956–959.
[38] X.H. Wang, X.H. Zhang, S.J. Tu, F. Shi, X. Zou, S. Yan, Z.G. Han, W.J. Hao, X.D. Cao, S.S. Wua, J. Heterocycl. Chem. 46 (2009) 832–836.
[39] Y. Yu, H. Guo, X. Li, J. Heterocycl. Chem. 48 (2011) 1264–1268.