[1] Y. Morimoto, F. Matsuda, H. Shirahama, Synlett, 1991, 202-203.
[2] J.P. Michael, Nat. Prod. Rep., 1997, 14, 605-618.
[3] D.G. Markees, V.C. Dewey, G.W. Kidder, J. Med. Chem., 1970, 13, 324-326.
[4] S.F. Campbell, J.D. Hardstone, M.J. Palmer, J. Med. Chem., 1998, 31, 1031-1035.
[5] M.P. Maguire, K.R. Sheets, K. McVety, A.P. Spada, A. Zilberstein, J. Med. Chem., 1994, 37, 2129-2137.
[6] Y.-L. Chen, K.-C. Fang, J.-Y. Sheu, S.-L. Hsu, C.-C. Tzeng, J. Med. Chem., 2001, 44, 2374-2377.
[7] M. Balasubramanian, J.G. Keay, In Comprehensive Heterocyclic Chemistry II. A.R. Katritzky, C.W. Rees and E.F.V. Scriven, Eds., Pergamon: New York, Vol. 5, 1996, p 245.
[8] X. Zhang, A.S. Shetty, S.A. Jenekhe, Macromolecules, 2000, 33, 2069-2082.
[9] S.A. Jenekhe, L. Lu, M.M. Alam, Macromolecules, 2001, 34, 7315-7324.
[10] R.H.F. Manske, M. Kulka, Org. React., 1953, 7, 59-98.
[11] V.V. Kouznetsov, L.Y.V. Mendez, C.M.M. Gomez, Curr. Org. Chem., 2005, 9, 141-146.
[12] L.J. Born, J. Org. Chem., 1972, 37, 3952-3953.
[13] P. Friedländer, Ber. Deutsch Chem. Ges., 1882, 15, 2572-2575.
[14] G.C. Muscia, M. Bollini, J.P. Carnevale, A.M. Bruno, S.E. Asis, Tetrahedron Lett., 2006, 47, 8811-8815.
[15] A. Shaabani, E. Soleimani, Z. Badri, Monatsh Chem., 2006, 137, 181-184.
[16] C.-S. Jia, Z. Zhang, S.-J. Tu, G.-W. Wang, Org. Biomol. Chem., 2006, 4, 104-110.
[17] G.-W. Wang, C.-S. Jia, Y.-W. Dong, Tetrahedron Lett., 2006, 47, 1059-1063.
[18] M. Narasimhulu, T.S. Reddy, K.C. Mahesh, P. Prabhakar, C.B. Rao, Y. Venkateswarlu, J. Mol. Catal. A: Chem., 2007, 266, 114-117.
[19] A. Shaabani, E. Soleimani, Z. Badri, Synth. Commun., 2007, 37, 629-635.
[20] M. Dabiri, M. Baghbanzadeh, M.S. Nikcheh, Monatsh Chem., 2007, 138, 1249-1252.
[21] A. Shaabani, A. Rahmati, Z. Badri, Z. Catal. Commun., 2008, 9, 13-16.
[22] S. Ghassamipour, A.R. Sardarian, Tetrahedron Lett., 2009, 50, 514-519.
[23] M. Barbero, S. Bazzi, S. Cadamuro, S. Dughera, Tetrahedron Lett., 2010, 51, 2342-2344.
[24] A. Hasaninejad, A. Zare, M. Shekouhy, J. Ameri-Rad, Green Chem., 2011, 13, 958-964.
[25] A.R. Kiasat, A. Mouradzadegun, S.J. Saghanezhad, Chin. J. Catal., 2013, 34, 1861-1868.
[26] D.S. Bose, R.K. Kumar, Tetrahedron Lett., 2006, 47, 813-816.
[27] M.A. Zolfigol, P. Salehi, A. Ghaderi, M. Shiri, Catal. Commun., 2007, 8, 1214-1218.
[28] M. Hosseini-Sarvari, Can. J. Chem., 2009, 87, 1122-1126.
[29] S. Sadjadi, S. Shiri, R. Hekmatshoar, Y.S. Beheshtiha, Monatsh Chem., 2009, 140, 1343-1347.
[30] S. Genovese, F. Epifano, M.C. Marcotullio, C. Pelucchini, M. Curini, Tetrahedron Lett., 2011, 52, 3474-3477.
[31] S.S. Palimkar, S.A. Siddiqui, T. Daniel, R.J. Lahoti, K.V. Srinivasan, J. Org. Chem., 2003, 68, 9371-9378.
[32]
F. Sadri,
A. Ramazani,
A. Massoudi,
M. Khoobi,
R. Tarasi,
A. Shafiee,
V. Azizkhani,
L. Dolatyari,
S.W. Joo,
Green Chem. Lett. Rev., 2014,
7, 257-264.
[33] A. Amoozadeh, M. Malmir, N. Koukabi, S. Otokesh, J. Chem. Res., 2015, 39, 694-697.
[34]
M. Shabanian,
M. Khoobi,
F. Hemati,
H.A. Khonakdar,
S.E. Sadat ebrahimi,
U. Wagenknecht,
A. Shafiee,
J. Ind. Eng. Chem., 2015,
24, 211-218.
[35] M. Khoobi, S.F. Motevalizadeh, Z. Asadgol, H. Forootanfar, A. Shafiee, M.A. Faramarzi, Mater. Chem. Phys., 2015, 149, 77-86.
[36] N. Dayyani, S. Khoee, A. Ramazani, Eur. J. Med. Chem., 2015, 98, 190-202.
[37] R. Meghyasi, J. Safaei-Ghomi, M.A. Sharif, J. Chem. Res., 2016, 40, 397-399.
[38] R.S. Varma, Green Chem., 1999, 1, 43-55.
[39] F. Nemati, M.M, Heravi, R. Saeedi Rad, Chin. J. Catal., 2012, 33, 1825-1831.
[40] A.R. Kiasat, J. Davarpanah, J. Mol. Catal. A: Chem., 2013, 373, 46-54.
[41] H. Naeimi, Z.S. Nazifi, J. Nanopart. Res., 2013, 15, 2026-2037.
[42] A. Khorshidi, S. Shariati, M. Aboutalebi, N. Mardazad, Iran. Chem. Commun., 2016, 4, 142-145.