[1]. Domling A., Wang W., Wang K. Chem. Rev., 2012, 112:3083
[2]. Jorissen W.P. Chem. Rev., 2006, 6:17
[3]. Rewcastle G.W., Bridges A.J., Fry D.W., Rubin J.R., Denny W.A. J. Med. Chem., 1997, 40:1820
[4]. Fry D.W., Becker M.A. Switzer R.L. Mol. Pharm., 1995, 47:810
[5]. Sanghvi Y.S., Larson S.B., Matsumoto S.S., Nord L.D., Smee D.F. Willis R.C., Avery T.H., Robins R.K., Revankar G.R J. Med. Chem., 1989, 32:629
[6]. Armstrong R.W., Combs A.P., Tempst P.A., Brown S.D., Keating T.A. Acc Chem. Res., 1996, 29:123
[7]. Tenser R.B., Gaydos A., Hay K.A. Antimicrob. Agents Chemother., 2001, 45:3657
[8]. Nizamuddin-Mishra M., Srivastava M.K., Khan M.H. Indian J. Chem., 2001, 40:49
[9]. Ajmal R.B., Rajendra S.D., Rupali S.S. Int. J. Pharma. Bio. Sci. 2014, 5:422
[10]. Balme G., Bossharth E. Monteiro N. Eur. J. Org. Chem., 2003, 21:4101
[11]. Dmytro H., Borys Z., Olexandr V., Lucjusz Z., Andrzej G., Roman L. Eur. J. Med.Chem., 2009, 44:1396
[12]. Sakuma Y., Hasegawa M., Kataoka K., Hoshina K., Yamazaki N., Kadota T. Chem. Abstr., 1991, 115:71646
[13]. Ezzati M., Khalafy J., Poursattar Marjani A., Prager R.H. Tetrahedron, 2017, 73:6587
[14]. Poursattar Marjani A., Khalafy J., Chitan M., Mahmoodi S. Iran. J. Chem. Chem. Eng., 2017, 36:1
[15]. Khalafy J., Majidi Arlan F., Soleimani Chalanchi Sh. J. Heterocycl. Chem.,2018, 55:149
[16]. Poursattar Marjani A., Khalafy J. Rostampoor A. J. Heterocycl. Chem., 2017, 54:648
[17]. Majidi Arlan F., Khalafy J., Maleki R. Chem. Heterocycl. Comp., 2018, 54:51
[18]. Javahershenas R., Khalafy J. J. Heterocycl. Chem., 2017, 54:3163
[19]. Javahershenas R., Khalafy J. Heterocycl Commun., 2018, 24:37
[21]. Perrin D.D., Armarego W.L.F., Purification of Laboratory Chemicals, Pergamon Press: Oxford, U.K., 1988, 15