Nano-Fe3O4@ZrO2-SO3H as highly efficient recyclable catalyst for the green synthesis of fluoroquinolones in ordinary or magnetized water
Subject Areas : Iranian Journal of CatalysisAhmad Nakhaei 1 , Abolghasem Davoodnia 2 , Sepideh Yadegarian 3
1 - Young Researchers and Elite Club, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
2 - Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
3 - Young Researchers and Elite Club, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
Keywords:
Abstract :
[1] R. Breslow, Acc. Chem. Res. 24 (1991) 159-164.
[2] P.B. Fernandes, N. Shipkowitz, R.R. Bower, K.P. Jarvis, J. Weisz, D.T. Chu, J. Antimicrob. Chemother. 18 (1986) 693-701.
[3] K. Fujimaki, T. Noumi, I. Saikawa, M. Inoue, S. Mitsuhashi, Antimicrob. Agents Chemother. 32 (1988) 827-833.
[4] B. Llorente, F. Leclerc, R. Cedergren, Bioorg. Med. Chem. 4 (1996) 61-71.
[5] Y.-S. Oh, C.-W. Lee, Y.-H. Chung, S.-J. Yoon, S.-H. Cho, J. Heterocycl. Chem. 35 (1998) 541-550.
[6] R. Stahlmann, H. Lode, Drugs 58 (1999) 37-42.
[7] B.A. Lipsky, C.A. Baker, Clin. Infect. Dis. 28 (1999) 352-361.
[8] D.C. Hooper, J.S. Wolfson, N. Engl. J. Med. 324 (1991) 384-394.
[9] J.S. Wolfson, D.C. Hooper, Clin. Microbiol. Rev. 2 (1989) 378-424.
[10] A. Aubry, X.-S. Pan, L.M. Fisher, V. Jarlier, E. Cambau, Antimicrob. Agents Chemother. 48 (2004) 1281-1288.
[11] T.D. Gootz, R. Zaniewski, S. Haskell, B. Schmieder, J. Tankovic, D. Girard, P. Courvalin, R.J. Polzer, Antimicrob. Agents Chemother. 40 (1996) 2691-2697.
[12] L.A. Mitscher, Chem. Rev. 105 (2005) 559-592.
[13] F. Dubar, G. Anquetin, B. Pradines, D. Dive, J. Khalife, C. Biot, J. Med. Chem. 52 (2009) 7954-7957.
[14] A.V. Shindikar, C.L. Viswanathan, Bioorg. Med. Chem. Lett. 15 (2005) 1803-1806.
[15] D. Sriram, A. Aubry, P. Yogeeswari, L.M. Fisher, Bioorg. Med. Chem. Lett. 16 (2006) 2982-2985.
[16] I.W. Davies, L. Matty, D.L. Hughes, P.J. Reider, J. Am. Chem. Soc. 123 (2001) 10139-10140.
[17] M. Ledoux, C. Pham-Huu, Catal. Today 15 (1992) 263-284.
[18] C.S. Gill, B.A. Price, C.W. Jones, J. Catal. 251 (2007) 145-152.
[19] A. Nakhaei, A. Davoodnia, S. Yadegarian, Heterocycl. Lett. 7 (2017) 35-44.
[20] A. Nakhaei, A. Davoodnia, S. Yadegarian, Russ. J. Gen. Chem. 86 (2016) 2870-2876.
[21] A. Nakhaei, A. Davoodnia, A. Morsali, Res. Chem. Intermed. 41 (2015) 7815-7826.
[22] A. Nakhaei, A. Davoodnia, Chin. J. Catal. 35 (2014) 1761-1767.
[23] A. Nakhaei, Russ. J. Gen. Chem. 87 (2017) 1850-1856.
[24] M. Bakherad, A. Keivanloo, M. Gholizadeh, R. Doosti, M. Javanmardi, Res. Chem. Intermed. 43 (2017) 1013-1029.
[25] M.M. Hosseini, E. Kolvari, Chem. Lett. 46 (2017) 53-55.
[26] E.E. Platero, M.P. Mentruit, Catal. Lett. 30 (1994) 31-39.
[27] C. Garkoti, J. Shabir, S. Mozumdar, New J. Chem. 41 (2017) 9291-9298.
[28] P.L. Patnam, M. Bhatt, R. Singh, S. Saran, S.L. Jain, RSC Adv. 6 (2016) 60888-60895.
[29] A. Sarkar, S.K. Biswas, P. Pramanik, J. Mater. Chem. 20 (2010) 4417-4424.
[30] G.-Y. Li, Y.-R. Jiang, K.-L. Huang, P. Ding, L.-L. Yao, Colloid. Surf. A 320 (2008) 11-18.
[31] A.P. Kumar, J.H. Kim, T.D. Thanh, Y.-I. Lee, J. Mater. Chem. B 1 (2013) 4909-4915.
[32] M.A. Navarra, F. Croce, B. Scrosati, J. Mater. Chem. 17 (2007) 3210-3215.
[33] P.G. Reddy, S. Baskaran, Tetrahedron Lett. 42 (2001) 6775-6777.
[34] K. Kawakami, K. Namba, M. Tanaka, N. Matsuhashi, K. Sato, M. Takemura, Antimicrob. Agents Chemother. 44 (2000) 2126-2129.
[35] K. Grohe, H. Heitzer, Liebigs Ann. Chem. 1987 (1987) 29-37.
[36] I. Hayakawa, T. Hiramitsu, Y. Tanaka, Chem. Pharm. Bull. 32 (1984) 4907-4913.
[37] B. Guruswamy, R. Arul, Lett. Drug Des. Discov. 10 (2013) 86-93.
[38] Y.R. Kumar, V.V.N.K.V. Prasad Raju, R.R. Kumar, S. Eswaraiah, K. Mukkanti, M.V. Suryanarayana, M.S. Reddy, J. Pharm. Biomed. Anal. 34 (2004) 1125-1129.