A simple and green approach for the synthesis of substituted dihydro-2-oxypyrroles catalyzed by nano-Fe3O4@SiO2/SnCl4 superparamagnetic nanoparticles

Subject Areas : Iranian Journal of Catalysis

Bi Bi Fatemeh Mirjalili ¹ , Reza Araqi ² , Seyed Ahmad Mohajeri ³

1 - Department of Chemistry, College of Science, Yazd University, Yazd, P.O. Box. 89195-741, I. R. Iran.
2 - Department of Chemistry, College of Science, Yazd University, Yazd, P.O. Box. 89195-741, I. R. Iran.
3 - Pharmaceutical Research Center, School of pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.

Received: 2017-08-05 Accepted : 2018-03-06 Published : 2019-03-01

Keywords:

References:

[1] T. Kawasuji, M. Fuji, T. Yoshinaga, A. Sato, T. Fujiwara, R. Kiyama, Bioorgan. Med. Chem. 15 (2007) 5487-5492.
[2] X. Luo, M. Shu, Y. Wang, J. Liu, W. Yang, Z. Lin, Molecules 17 (2012) 2015-2029.
[3] C. Peifer, R. Selig, K. Kinkel, D. Ott, F. Totzke, C. Schächtele, R. Heidenreich, M. Röcken, D. Schollmeyer, S. Laufer, J. Med. Chem. 51 (2008) 3814-3824.
[4] T.R. Reddy, C. Li, X. Guo, H.K. Myrvang, P.M. Fischer, L.V. Dekker, J. Med. Chem. 54 (2011) 2080-2094.
[5] W. R. Li, S.T. Lin, N.M. Hsu, M.S. Chern, J. Org. Chem. 67 (2002) 4702-4706.
[6] A. Kolocouris, G.B. Foscolos, G. Fytas, J. Neyts, E. Padalko, J. Balzarini, R. Snoeck, G. Andrei, E. De Clercq, J. Med. Chem. 39 (1996) 3307-3318.
[7] A.S. Demir, F. Aydogan, I.M. Akhmedov, Tetrahedron Asym. 13 (2002) 601-605.
[8] Z. Feng, X. Li, G. Zheng, L. Huang, Bioorg. Med. Chem. Lett. 19 (2009) 2112-2115.
[9] L. Zhang, Y. Tan, N.X. Wang, Q.Y. Wu, Z. Xi, G.F. Yang, Bioorg. Med. Chem. 18 (2010) 7948-7956.
[10] S. Tarnavsky, G. Dubinina, S. Golovach, S. Yarmoluk, Biopolym. Cell. 19 (2003) 548-552.
[11] D. Albrecht, B. Basler, T. Bach, J. Org. Chem. 73 (2008) 2345-2356.
[12] A. Dömling, Chem. Rev. 106 (2006) 17-89.
[13] A. Bamoniri, B.F. Mirjlili, R. Tarazian, Monatsh. Chem.146 (2015) 2107-2115.
[14] A.T. Khan, A. Ghosh, M. M. Khan, Tetrahedron Lett. 53 (2012) 2622-2626.
[15] L. Lv, S. Zheng, X. Cai, Z. Chen, Q. Zhu, S. Liu, ACS Comb. Sci. 15 (2013) 183-192.
[16] B.F. Mirjalili, R. Zare Reshquiyea, RSC Adv. 5 (2015)15566-15571.
[17] S. Rana, M. Brown, A. Dutta, A. Bhaumik, C. Mukhopadhyay, Tetrahedron Lett. 54 (2013) 1371-1379.
[18] S.S. Sajadikhah, N. Hazeri, M.T. Maghsoodlou, S.M. Habibi-Khorassani, K. Khandan-Barani, J. Chem. Res. 37 (2013) 40-42.
[19] N. Salehi, B.F. Mirjalili, RSC Adv. 7 (2017) 30303-30309.
[20] M. Nickraftar, N. Najafi Hajivar, J. Aboonajmi, E. Fereidooni, Res. Chem. Intermed. 42 (2016) 2899-2908.
[21] S.S. Sajadikhah, M.T. Maghsoodlou, RSC Adv. 4 (2014) 43454-43459.
[22] L. Lv, S. Zheng, X. Cai, Z. Chen, Q. Zhu, S. Liu S, ACS Comb. Sci. 15 (2013) 183-192;
[23] S.S. Sajadikhah, N. Hazeri, M.T. Maghsoodlou, S.M. Habibi-Khorassani, J. Chin. Chem. Soc. 60 (2013) 1003-1006.
[24] S.S. Sajadikhah, M.T. Maghsoodlou, N. Hazeri, Chin. Chem. Lett. 25 (2014) 58-60.
[25] Q. Zhu, H. Jiang, J. Li, S. Liu, C. Xia, M. Zhang, (2009) J. Comb. Chem. 11 (2009) 685-696.
[26] S.S. Sajadikhah, N. Hazeri, Res. Chem. Intermed. 40 (2014) 737-748.
[27] N. Hazeri, S.S. Sajadikhah, M.T. Maghsoodlou, S. Mohamadian-Souri, M. Norouzia, M. Moein, J. Chin. Chem. Soc. 61 (2014) 217-220.
[28] S.S. Sajadikhah, N. Hazeri, M.T. Maghsoodlou, S.M. Habibi-Khorassani, A. Beigbabaei, A.C. Willis, J. Iran. Chem. Soc. 10 (2013) 863-871.
[29] J.N. Zhang, X.H. Yang, W.J. Guo, B. Wang, Z.H. Zhang, Synlett 28 (2017) 734-740.
[30] B.F. Mirjalili, H. Jorsarraie, H. Akrami, Iran. J. Catal. 7 (2017) 201-205.
[31] B.F. Mirjalili, A. Bamoniri, Z. Fazeli, Iran. J. Catal. 6 (2016) 253-259.
[32] B.F. Mirjalili, A. Bamoniri, M.A. Mirhoseini, Iran. J. Catal. 6 (2016) 23-27.
[33] B.F. Mirjalili, A. Bamoniri, S. Fouladgar, Polycycl. Aromat. Compd. 37 (2017) 345-361.
[34] A. Bamoniri, S. Fouladgar, RSC Adv. 5 (2015) 78483-78490.