Document Type : Original Research Article

Authors

Department of Chemistry, Payame Noor University, P.O. BOX 19395-4697 Tehran, Iran

10.30473/icc.2020.55566.1670

Abstract

Xanthenes have been considered in medicine and biology. Their medicinal properties include antiviral, antibacterial, anti-inflammatory, and therapeutic photodynamic activities, as well as the antagonist for paralytic action. 1,8-Dioxo-octahydroxanthenes have synthesized good yields via a reaction of aldehydes and dimedone in the presence of  cerium oxide/aluminum oxide nano-catalyst as a catalyst. High efficiency, short time and reuseability of catalyst are the advantages of this method.

Graphical Abstract

Nano- cerium oxide/aluminum oxide as an efficient catalyst for the synthesis of xanthene derivatives as potential antiviral and anti-inflammatory agents

Keywords

Main Subjects

[1] A. Walter, Am. Soc. Clinical. Oncolog., 2010, 35, 469–474.
[2] M. Sherafat, A. Shokuhi Rad, M. Arjomand, A. Heydarinasab, M. Peyravi, M. Mirzaei, Curr. Appl. Phys., 2018, 18, 1059-1065.
[3] A. Allahresani, F. Ghorbanian, M.A. Nasseri, Iran. Chem. Commun., 2020, 8, 212-229.
[4] S.C. Azimi, E. Abbaspour-Gilandeh, Iran. Chem. Commun., 2016, 4, 236-258.
[5] R. Khoeiniha, A. Ezabadi, A. Olyaei, Iran. Chem. Commun., 2016, 4, 273-282.
[6] B. Zakerinasab, M. Nasseri, H. Hassani, Iran. Chem. Commun., 2016, 4, 133-235.
[7] A. Davoodnia, H. Nakhaei, J. Chem. Rev., 2019, 1, 139-153.
[8] A. Nakhaei, S. Yadegarian, J. Appl. Chem. Research., 2017, 11, 72-83.
[9] A. Davoodnia, Russ. J. General. Chem., 2016, 86, 2849-2854.
[10] A. Nakhaei, A. Davoodnia, A. Morsali, Research. Chem. Intermediat., 2015, 41, 7815-7826.
[11] A. Davoodnia, A. Nakhaei, S. Basafa, N. Tavakoli-Hoseini, Adv. J. Chem-Sect. A., 2018, 1, 96-104.
[12] E. Ezzatzadeha, S. Nazaraliana , F. Sheikholeslami, Iran. J. Org. Chem., 2017, 9, 2057-2065.
[13] M.P. Lande, T. Gadekar, G. Pawar, R. Magar, Bull. Chem. React. Eng. Catal., 2018, 3, 436-437. 
[14] Sh. Babadoust, Int. J. Chem. Biochem. Sci., 2014, 6, 72-73.  
[15] F. Darviche, S. Balalaie, F. Chadegani, P. Salehi, Synth. Commun., 2007, 37,1059-1063.
[16] S. Deshmukh, G.U. Kadam, K. Shisodia, M.V. Int. J. Chem. Phys. Scienc., 2018, 7, 75-76
[17] F. Noori Sadeh, M. Fatahpour, N. Hazeri, M. Taher maghsoodlou, M. Lashkari, Acta. Chemica. Iasi., 2017, 25, 24-37.
[18] K.P. Nandre, V.S. Patil, S. Bhosale, Chin. Chem. Lett., 2011, 22, 777-780    
[19] G. Ertl, H. Knozinger, J. Weitkamp, Handbook of Heterogeneous Catalysis, VCH. Weinheim, 1997, 1, 16.
[20] V. Polshettiwar, S. Rajender, Green. Chem., 2010, 12, 743–754.
[21] S. Pabbaraja, Chin. Chem. Lett., 2008, 19, 771-777.
[22] R.R. Muthuchudarkodi, Int. J. Sci. Research., 2016, 5, 543-547.  
[23] T. Hideo, Chemical Abstract., 1981, 95, 80922b.   
[24] J.P. Poupelin, G. Saint-Ruf, O. Foussard-Blanpin, G. Narcisse, G. Uehida, R. Lacroix, Europ. J. Med. Chem., 1978, 13, 67-71.     
[25] G. Saint-Ruf, H.T. Hieu, Bull. Chem. Soc. Jap., 1972, 7, 83-86. 
[26] A. Cvetkovic, J. Adrie, J. Straathof, K. Rajamani, A.M. Luuk, Derwielen. Langmuir., 2005, 21, 1475-1478.
[27] J.F. Callan, P. De Silva, D. Magri, Tetrahedron., 2005, 61, 8551-8588.