Synthesis of bis-thiazolidinones catalyzed by nano-NiZr4(PO4)6 under microwave irradiation
Subject Areas : Iranian Journal of Catalysis
Javad Safaei-Ghomi
1
(Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan 51167, I. R. Iran.)
Hossein Shahbazi-Alavi
2
(Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan 51167, I. R. Iran. |
Young Researchers and Elite Club, Kashan Branch, Islamic Azad University, Kashan, Iran.)
Seyed Hadi Nazemzadeh
3
(Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan 51167, I. R. Iran. |
Young Researchers and Elite Club, Kashan Branch, Islamic Azad University, Kashan, Iran.)
Keywords:
Abstract :
[1] J. Senkiv, N. Finiuk, D. Kaminskyy, D. Havrylyuk, M. Wojtyra, I. Kril, A. Gzella, R. Stoika, R. Lesyk, Eur. J. Med. Chem. 117 (2016) 33-46.
[2] H.M.A. Ashour, I.M. El-Ashmawy, A.E. Bayad, Monatsh. Chem. 147 (2016) 605-618.
[3] R. Nechak, S.A. Bouzroura, Y. Benmalek, L. Salhi, S.P. Martini, V. Morizur, E. Dunach, B.N. Kolli, Synth. Commun. 45 (2015) 262-672.
[4] D.D. Subhedar, M.H. Shaikh, M.A. Arkile, A. Yeware, D. Sarkar, B.B. Shingate, Bioorg. Med. Chem. Lett. 26 (2016) 1704-1708.
[5] M.V. Diurno O. Mazzoni, G. Correale, I.G. Monterrey, A. Calignano, G.L. Rana, A. Bolognese, Il Farmaco 54 (1999) 579–583.
[6] R.K. Rawal, Y.S. Prabhakar, S.B. Katti, E. De Clercq, Bioorg. Med. Chem. Lett. 13 (2005) 6771-6776.
[7] R.K. Rawal, R. Tripathi, S.B. Katti, C. Pannecouque, E. De Clercq, Bioorg. Med. Chem. 15 (2007) 1725-1731.
[8] D. Kumar, M. Sonawane, B. Pujala, V.K. Jain, A.K. Chakraborti, Green Chem. 15 (2013) 2872-2884.
[9] S.P. Shrivastava, N. Seelam, R. Rai, J. Chem. 9 (2012) 825-831.
[10] A. Mobinikhaledi, A.K. Amiri, Lett. Org. Chem. 10 (2013) 764-769.
[11] R.M. Abdel-Rahman, T.E. Ali, Monatsh. Chem. 144 (2013) 1243-1252.
[12] J. Safaei‑Ghomi, P. Babaei, H. Shahbazi‑Alavi, S.G. Pyne, A.C. Willis, J. Iran. Chem. Soc. 13 (2016) 1439-1448.
[13] M.B. Gawande, S.N. Shelke, R. Zboril, R.S. Varma, Acc. Chem. Res. 47 (2014) 1338−1348.
[14] F.A. Bassyouni, S.M. Abu-Bakr, M.A. Rehim, Res. Chem. Intermed. 38 (2012) 283–322.
[15] J. Safaei-Ghomi, H. Shahbazi-Alavi, P. Babaei, H. Basharnavaz, S.G. Pyne, A.C. Willis, Chem. Heterocycl. Compd. 52 (2016) 288–293.
[16] M.B. Gawande, P.S. Branco, R.S. Varma, Chem. Soc. Rev. 42 (2013) 3371-3393.
[17] A. Dastan, A. Kulkarni, B. Torok, Green Chem. 14 (2012) 17–37.
[18] A. Sharma, P. Appukkuttan, E.V. Eycken, Chem. Commun. 48 (2012) 1623–1637.
[19] J. Safaei-Ghomi, E. Afkhami, H. Shahbazi-Alavi, A. Ziarati, Iran. J. Catal. 5 (2015) 321-326.
[20] N. Gorodylova, V. Kosinová, Z. Dohnalová, P. Sulcová. Dyes Pigm. 98 (2013) 393-404.
[21] J. Safaei-Ghomi, M. Asgari-Kheirabadi, H. Shahbazi-Alavi, A. Ziarati, Iran. J. Catal. 6 (2016) 319-324.
[22] I.G. Trubach, A.I. Beskrovnyi, A.I. Orlova, V.A. Orlova, V.S. Kurazhkovskaya, Crystallogr. Rep. 49 (2004) 895–898.
[23] A.R. Zaripov, V.A. Orlova, V.I. Petkov, O.M. Slyunchev, D.D. Galuzin, S.I. Rovnyi, Russ. J. Inorg. Chem. 54 (2009) 45-51.
[24] T. Previtera, M. Basile, M.G. Vigorita, G. Fenech, F. Occhiuto, C. Circosta, R.C. de Pasquale, Eur. J. Med. Chem. 22 (1987) 67-74.
[25] V.V. Kouznetsov, D.F. Amado, A. Bahsas, J. Amaro‐Luis, J. Heterocycl. Chem. 43 (2006) 447-452.
