10.22034/ajgc.2018.65773

[1]. Omolo J.J., Johnson M.M., van Vuuren S.F., de Koning C.B. Bioorg Med Chem Lett., 2011, 21:7085
[2]. Limsuwan S., Trip E.N., Kouwen T.R.H.M., Piersma S., Hiranrat A., Mahabusarakam W.,,
Voravuthikunchai S.P., van Dijl J.M., Kayser O. Phytomedicine, 2009, 16:645
[3]. Poupelin J.P., Saint-Ruf G., Foussard-Blanpin O., Narcisse G., Uchida-Ernouf G., Lacroix R. Eur. J. Med. Chem., 1978, 13:67
[4]. Ahmad M., King T.A., Ko D.K., Cha B.H., Lee J. J. Phys. D: Applied Physics, 2002, 35:1473
[5]. Knight C.G., Stephens T. Biochem. J., 1989, 258:683
[6]. Kitahara Y., Tanaka K. Chem. Commun., 2002, 932 DOI:10.1039/B110514K
[7]. Nagarapu L., Kantevari S., Mahankhali V.C., Apuri S. Catal. Commun., 2007, 8:1173
[8]. Pasha M.A., Jayashankara V.P. Bioorganic Med. Chem. Lett., 2007, 17:621
[9]. Bigdeli M.A., Heravi M.M., Mahdavinia G.H. J Mol Catal A: Chem., 2007, 275:25
[10]. Patil S.B., Bhat R.P., Samant S.D. Synth. Commun., 2006, 36:2163
[11]. Wang J.Q., Harvey R.G. Tetrahedron, 2002, 58:5927
[12]. Knignt D.W., Little P.B. Synlett, 1998, 10:1141
[13]. Kuo C.W., Fang J.M. Synth. Commun., 2001, 31:877
[14]. Jha A., Beal J. Tetrahedron Lett., 2004, 45:8999
[15]. Rao G.B.D., Kaushik M.P., Halve A.K. Tetrahedron Lett., 2012, 53:2741
[16]. Kumar P.S., Sreenivasulu N., Sunil Kumar B., Rajitha B., Narsimha Reddy P., Thirupathi Reddy Y. Arkivoc, 2006, xii:46
[17]. Rajitha B., Sunil Kumar B., Thirupathi Reddy Y., Narsimha Reddy P., Sreenivasulu N. Tetrahedron Lett., 2005, 46:8691
[18]. Nazari S., Keshavarz M., Karami B., Iravani N., Vafaee-Nezhad M. Chin. Chem. Lett,. 2013, 25:317
[19]. Shirini F., Ghaffari Khaligh N. Dyes Pigm., 2012, 95:789
[20]. Dabiri M., Azimi S.C., Bazgir A. Chem. Pap., 2008, 62:522
[21]. Zolfigol M.A., Khakyzadeh V., Moosavi-Zare A.H., Zare A., Azimi S.B., Asgari Z., Hasaninejad A.R. C. R. Chim., 2012, 15:719
[22]. Shaterian H.R., Ghashang M. J. Braz. Chem. Soc., 2008, 19:1053
[23]. Rezayati S., Mirzajanzadeh E., Seifournia H. Asian J. Green Chem., 2017, 1:24
[24]. Haeri H.S., Rezayati S., Rezaee Nezhad E., Darvishi H. Res. Chem. Intermed., 2016, 42:4773
[25]. Moosavi-Zare A.R., Zolfigol M.A., Zare M., Zare A., Khakyzadeh V. Journal Molecular Liquids, 2015, 211:373
[26]. Rezayati S., Abbasi Z., Rezaee Nezhad E., Hajinasiri R., Farrokhnia A. Res. Chem. Intermed., 2016, 42:7597
[27]. Rezaee Nezhad E., Sahhadifar S., Abbasi Z., Rezayati S. J. Sci. I. R. Iran, 2004, 25:127
[28]. Rezaee Nezhad E., Abbasi Z., Sajjadifar S. Sci. Iran., 2015, 22:903
[29]. Sajjadifar S., Abbasi Z., Rezaee Nezhad E., Rahimi Moghaddam M., Karimian S., Miri S. J. Iran Chem. Soc., 2014, 11:335
[30]. Rezayati S., Abbasi Z., Rezaee Nezhad E., Hajinasir R., Soleymani Chalanchi Sh. Org. Chem. Res., 2016, 2:162
[31]. Sajjadifar S., Rezayati S., Shahriari A., Abbaspour S. Appl. Organometal. Chem., 2017, https://doi.org/10.1002/aoc.4172
[32]. Sajjadifar S., Rezayati S., Arzehgar Z., Abbaspour S., Torabi Jafroudi M. J. Chin. Chem. Soc., 2018, https://doi.org/10.1002/jccs.201800036
[33]. Soleiman-Beigi M., Arzehgar Z. Monatsh Chem., 2016, 147:1759
[34]. Sajjadifar S., Arzehgar Z., Ghayuri A. J. Chin. Chem. Soc., 2018, 65:205

[35]. Abbasi Z., Rezayati S., Bagheri M., Hajinasiri R. Chin. Chem Lett,. 2017, 28:75