Synthesis and in vitro antibacterial study of dihydropyrano[3,2-c]chromene derivatives by nano fluoro apatite doped with Mg and Si as a cooperative catalyst
Subject Areas : Iranian Journal of CatalysisElmira Jahangard 1 , Leila Khazdooz 2 , Amin Zarei 3
1 - Department of Science, Isfahan (Khorasgan) Branch, Islamic Azad University, Isfahan 81595-158, Iran.
2 - Department of Science, Isfahan (Khorasgan) Branch, Islamic Azad University, Isfahan 81595-158, Iran.|Laser and Biophotonics in Biotechnologies Research Center, Isfahan (Khorasgan) Branch, Islamic Azad University, Isfahan 81595-158, Iran.
3 - Department of Science, Fasa Branch, Islamic Azad University, PO Box No. 364, Fasa, Fars 7461713591, Iran.
Keywords:
Abstract :
[1] C. Simon, T. Constantieux, J. Rodriguez, Eur. J. Org. Chem. 2004 (2004) 4957–4980.
[2] C.O. Kappe, Acc. Chem. Res. 33 (2000) 879–888.
[3] D.J. Ramon, M. Yus, A. Dömling, I. Ugi, J. Zhu, H. Bienayme, Angew. Chem. Int. Ed. 44 (2005) 1602–1634.
[4] A. Ulaczyk-Lesanko, D.G. Hall, Curr. Opin. Chem. Biol. 9 (2005) 266–276.
[5] B.B. Toure, D.G. Hall, Chem. Rev. 109 (2009) 4439–4486.
[6] R.M. Okasha, F.F. Albalawi, T.H. Afifi, A.M. Fouda, A.A.M. Al-Dies, A.M. El-Agrody, Molecules 21 (2016) 1–15.
[7] M. Li, X. Zhao, W. Yang, F. Zhong, L. Yuan, Q. Ren, Tetrahedron Lett. 59 (2018) 3511–3515.
[8] S. Nasri, M. Bayat, J. Mol. Struct. 1164 (2018) 77–83.
[9] F.A. Galil, B.Y. Riad, S.M. Sherif, M.H. Elnagdi, Chem. Lett. (1982) 1123–1126.
[10] E.A.A. Hafez, M.H. Elnagdi, A.G.A. Elagamey, F.M.A.A. El-Taweel, Heterocycles 26 (1987) 903–907.
[11] M.A. Sofan, F.M. El‐Taweel, A.G.A. Elagamey, M.H. Elnagdi, Justus Liebigs Ann. Chem. 1989 (1989) 935–936.
[12] L. Bonsignore, G. Loy, D. Secci, A. Calignano, Eur. J. Med. Chem. 28 (1993) 517–520.
[13] T. Raj, R.K. Bhatia, R.K. Sharma, V. Gupta, D. Sharma, M.P.S. Ishar, Eur. J. Med. Chem. 44 (2009) 3209–3216.
[14] L.L. Adreani, E. Lapi, Boll. Chim. Farm. 99 (1960) 583–586.
[15] G. Brahmachari, ACS Sustain. Chem. Eng. 3 (2015) 2058–2066.
[16] A. Burgard, H.-J. Lang, U. Gerlach, Tetrahedron 55 (1999) 7555–7562.
[17] J.M. Evans, C.S. Fake, T.C. Hamilton, R.H. Poyser, G.A. Showell, J. Med. Chem. 27 (1984) 1127–1131.
[18] J.M. Evans, C.S. Fake, T.C. Hamilton, R.H. Poyser, E.A. Watts, J. Med. Chem. 26 (1983) 1582–1589.
[19] J.M. Khurana, S. Kumar, Tetrahedron Lett. 50 (2009) 4125–4127.
[20] H. Mehrabi, H. Abusaidi, J. Iran Chem Soc. 7 (2010) 890–894.
[21] H.-J. Wang, J. Lu, Z.-H. Zhang, Monatsh. Chem. 141 (2010) 1107–1112.
[22] A.T. Khan, M. Lal, S. Ali, M.M. Khan, Tetrahedron Lett. 52 (2011) 5327–5332.
[23] J.M. Khurana, B. Nand, P. Saluja, Tetrahedron 66 (2010) 5637–5641.
[24] Y. Wang, H. Ye, G. Zuo, J. Luo, J. Mol. Liq. 212 (2015) 418–422.
[25] H. Mehrabi, M. Kazemi-Mireki, Chinese Chem. Lett. 22 (2011) 1419–1422.
[26] K. Niknam, A. Piran, Green Sustain. Chem. 3 (2013) 1-8.
[27] M. Khaleghi-Abbasabadi, D. Azarifar, Res. Chem. Intermed. 45 (2019) 2095–2118.
[28] L. Nazemi Nasirmahale, O. Goli Jolodar, F. Shirini, H. Tajik, Polycycl. Aromat. Comp. (2019) doi:10.1080/10406638.2019.1576748.
[29] E. Mollashahi, M. Nikraftar, J. Saudi Chem. Soc. 22 (2018) 42–48.
[30] M. Ghashang, S.S. Mansoor, L. Shams Solaree, A. Sharifian-esfahani, Iran. J. Catal. 6 (2016) 237–243.
[31] B. Maleki, Org. Prep. Proced. Int. 48 (2016) 303–318.
[32] T. Ahmadi, A. Monshi, V. Mortazavi, M.H. Fathi, S. Sharifi, B.H. Beni, A.M. Abed, M. Kheradmandfard, A. Sharifnabi, Ceram. Int. 40 (2014) 8341–8349.
[33] L. Khazdooz, A. Zarei, T. Ahmadi, H. Aghaei, N. Nazempour, L. Golestanifar, N. Sheikhan, Reac. Kinet. Mech. Catal. 122 (2017) 229–245.
[34] L. Khazdooz, A. Zarei, T. Ahmadi, H. Aghaei, L. Golestanifar, N. Sheikhan, Res. Chem Int. 44 (2018) 93-115.
[35] B. Karami, M. Kiani, Monatsh. Chem. 147 (2016) 1117–1124.
[36] S. Abdolmohammadi, S. Balalaie, Tetrahedron Lett. 48 (2007) 3299–3303.
[37] H. Emtiazi, M.A. Amrollahi, Bulg. Chem. Commun. 49 (2017) 478–482.
[38] C.V. Subbareddy, S. Sundarrajan, A. Mohanapriya, R. Subashini, S. Shanmugam, J. Mol. Liq. 251 (2018) 296–307.
[39] A. Aminkhani, M. Talati, R. Sharifi, F. Chalabian, F. Katouzian, J. Heterocycl. Chem. 56 (2019) 1812-1819.