[1] J.G. Lambardino, E.H. Wiseman, J. Med. Chem., 1974, 17, 1182-1188.
[2] A. Chawla, A. Sharma, A.K. Sharma, Der Pharm. Chem., 2012, 4, 116-140.
[3] J.C. Lee, J.T. Laydon, P.C. McDonnell, T.F. Gallagher, S. Kumar, D. Green, D. McNulty, M.J. Blumenthal, J.R. Keys, S.W.R. Vatter, J.E. Strickler, M.M. McLaughlin, I.R. Siemens, S.M. Fisher, G.P. Livi, J.R. White, J.L. Adams, P.R. Young, Nature, 1994, 372, 739-746.
[4] L.L. Chang, K.L. Sidler, M.A. Cascieri, S. Laszlo,G. Koch, B. Li, M. Maccoss, N. Mantlo,S. Okeefe, M. Pang, A. Rolando, W.K. Hangmann, Bioorg. Med. Chem. Lett., 2001, 11, 2549-2553.
[5] A.K. Takle, M.J.B. Brown, S. Davies, D.K. Dean, G. Francis, A. Gaiba, A.W. Hird, F.D. King, P.J. Lovell, A. Naylor, A.D. Reith, J.G. Steadman, D.M. Wilson, Bioorg. Med. Chem. Lett., 2006, 16, 378-381.
[6] M. Antolini, A. Bozzoli, C. Ghiron, G. Kennedy, T. Rossi, A. Ursini, Bioorg. Med. Chem. Lett., 1999, 9, 1023-1028.
[7] R. Schmierer, H. Mildenberger, H. Buerstell, German Patent, 1987, 3, 61464; Chem. Abstr., 1988, 108, 37838.
[8] M. Antolini, A. Bozzoli, C. Ghiron, G. Kennedy, T. Rossi, A. Ursini, Bioorg. Med. Chem. Lett., 1999, 9, 1023-1028.
[9] J. Heeres, L.J.J. Backx, J.H. Mostmans, J. Van Custem, J. Med. Chem., 1979, 22, 1003-1005.
[10] T. Maier, R. Schmierer, K. Bauer, H. Bieringer, H. Buerstell, B. Sachse, U.S. Patent 1989, 4820335; Chem. Abstr., 1989, 111, 19494w.
[11] A.R. Moosavi-Zare,, H. Goudarziafshar, Z. Jalilian, Prog. Chem. Biochem. Res., 2019, 2, 59-63.
[12] M. Aghazadeh, Prog. Chem. Biochem. Res., 2019, 2, 34-39.
[13] M. Asif, I. Mohd, Prog. Chem. Biochem. Res., 2019, 2, 192-210.
[14] B. Maleki, S. Sedigh Ashrafi, J. Mexican Chem. Soc., 2014, 58, 76-81.
[15] B. Maleki, H.K. Shirvan, F. Taimazi, E. Akbarzadeh, Inter. J. Org. Chem., 2012, 2, 93-99.
[16] M.M. Heravi, N. Karimi, S. Pooremami, Adv. J. Chem. A, 2019, 2, 73-78.
[17] B. Maleki, H. Keshvari, A. Mohammadi, Orient. J. Chem. A, 2012, 28, 1207-1212.
[18] A. Mohammadi, H. Keshvari, R. Sandaroos, B. Maleki, H. Rouhi, H. Moradi, Z. Sepehr, S. Damavandi, Appl. Catal. A: Gen., 2012, 429, 73-78.
[19] B. Maleki, H. Eshghi, A. Khojastehnezhad, R. Tayebee, S.S. Ashrafi, G.E. Kahoo, F. Moeinpour, RSC Advances, 2015, 5, 64850-64857.
[20] M.M. Heravi, H. Hamidi, N. Karimi, A. Amouchi, Adv. J. Chem. A, 2018, 1, 1-6.
[21] B. Maleki, G.E. Kahoo, R. Tayebee, Org. Prep. Proced. Int., 2015, 47, 461-472.
[22] H. Ramshini, R. Tayebee, A. Bigi, F. Bemporad, C. Cecchi, F. Chiti, Int. J. Mol. Sci., 2019, 20, 5558-5576.
[23] R. Tayebee, M. FattahiAbdizadeh, N. Erfaninia, A. Amiri, M. Baghayeri, R.M. Kakhki, B. Maleki, E. Esmaili, Appl. Organomet. Chem., 2019, 33, e4959.
[24] R. Tayebee, A.F. Lee, L. Frattini, S. Rostami, Catalysts, 2019, 9, 409-416.
[25] N. Erfaninia, R. Tayebee, E.L. Foletto, M.M. Amini, M. Dusek, F.M. Zonoz, Appl. Organomet. Chem., 2018, 32, e4047.
[26] N. Erfaninia, R. Tayebee, M. Dusek, M.M. Amini, Appl. Organomet. Chem., 2018, 32, e4307.
[27] R. Tayebee, A. Pejhan, H. Ramshini, B. Maleki, N. Erfaninia, Z. Tabatabaie, E. Esmaeili, Appl. Organomet. Chem., 2018, 32, e3924.
[28] F. Javadi, R. Tayebee, B. Bahramian, Appl. Organomet. Chem., 2017, 31, e3779.
[29] F. Javadi, R. Tayebee, Iran. J. Catal., 2017, 7, 283-292.
[30] B. Mirjalili, A. Bamoniri, N. Mohaghegh, Curr. Chem. Lett., 2013, 2, 35-42.
[31] J.N. Sangshetti, N.D. Kokare, S.A. Kotharkar, D.B. Shinde, Chin. Chem. Lett., 2008, 19, 762-766.
[32] J.N. Sangshetti, N.D. Kokare, S.A. Kotharkar, D.B. Shinde, Monat. für Chem.-Chem. Mon, 2008, 139, 125-127.
[33] S.D. Jadhav, N.D. Kokare, S.D. Jadhav, J. Heterocycl. Chem., 2008, 45, 1461-1464.
[34] K.F. Shelke, S. Sapkal, S. Sonal, B.R. Madje, B.B. Shingate, M.S. Shingare, Bull. Kor. Chem. Soc., 2009, 30, 1057-1060.
[35] R.S. Joshi, P.G. Mandhan, M.U. Shaikh, R.P. Kale, C.H. Gill, Chin. Chem. Lett., 2010, 21, 429-432.
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