Mesolite catalyzed one pot synthesis of quinoline-3-carbonitrile derivatives

Subject Areas : Iranian Journal of Catalysis

Ganesh Pawar ¹ (Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India.)
Rameshwar Magar ² (Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India.)
Machhindra Lande ³ (Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.), 431004, India.)

Received: 2015-12-29 Accepted : 2016-03-29 Published : 2016-09-01

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References:

[1] R.C. Cioc, E. Ruijter, V.A. Romano, Green Chem. 16 (2014) 2958-2975.
[2] P.M. Joseph, Nat. Prod. Rep. 24 (2007) 223-246.
[3] S. Amish, Raj. Dilipsinh, J. Saudi Chem. Soc. 19 (2015) 73-82.
[4] I. A. Saleh, M.A. Areej, M.A. Ahmed, N. Eman, M.G. Mostafa, Eur. J. Med. Chem. 45 (2010) 738-744.
[5] A.L. Don, C.R Elena, B. Benoit, H. Hasin-Hung, D. Latasha, J. Laure, E. Mourad, B. Katja, L.W. David, D. C. Elisabeth, Org. Biomol. Chem. 10 (2012) 6375.
[6] L.Z. Shu, Z. Xin, J.Z. Shi, H. Yu. Hong, G. Ping, Chin. Chem. Lett. 21 (2010) 939-942.
[7] P. Natasha, N. Raja, E. Katja, L. William, K.Z. Grace, K. Marijeta, D. Marie-Hélène, H. Marijana, Eur. J. Med. Chem. 80 (2014) 218-227.
[8] K.S. Kumar, S.K. Kumar, B.Y. Shreenivas, D.R. Gorja, R. Kapavarapu, D. Rambabu, G.R. Krishna, C.M. Reddy, M.V. Basaveswara, K.V.L. Parasa, M. Pal, Bioorg. Med. Chem. 20 (2012) 2199-2207.
[9] E. Debroye, G. Dehaen, V.S. Eliseeva, S, V.L. Elst, N. R. Muller, K. Binnemans, N.T. Parac-Vogt, Dalton Trans. 41 (2012) 10549-10556.
[10] A.K. Salman, M.A. Abdullah, H.A. Sadd, M.F. Hassan, A.E. Sammy, Spectrochim. Acta, Part A 133 (2014) 141-148.
[11] A. Khalafi-Nezhad, S. Sarikhani, E. Shaikhi Shahidzadeh, F. Panahi, Green Chem. 14 (2012) 2876-2884.
[12] G.K. Nader, Chin. J. Cat. 35 (2014) 1858-1863.
[13] G.M. Ziarani, N. Hosseini Nasab, M. Rahimifard, A. Abolhasani Soorki, J. Saudi Chem. Soc. 9 (2015) 676-681.
[14] Y. Venkatewarlu, K.R. Kumar, P. Leelavati, Org. Commun. 5 (2012) 120-127.
[15] E.A. Gilandeh, S.C. Azimia, K.R. Moghadama, A.M. Barkchaib, Iran. J. Catal. 3 (2013) 15-20.
[16] A. Chandra, S. Upadhyay B. Singh, N. Sharma, M.R. Singh, Tetrahedron Lett. 67 (2011) 9219-9224.
[17] J. Mcnulty, R. Vemula, C. Bordon, R. Yolken, J.B. Lorraine, Org. Biomol. Chem. 12 (2014) 255-260.
[18] D.W. Breck, Zeolite Molecular Sieves, Structure, Chemistry and Use. John Wiley & Sons, New York, London, Sydney, Toronto, 1974.
[19] S.M. Baghbanian, N. Rezaei, H. Tashakkorin, Green Chem. 15 (2013) 3446-3458.
[20] E. Erdem, N. Karapinar, R. Donat, J. Colloid Interface Sci. 280 (2004) 309-314.
[21] S. Wang, Z.H. Zhu, J. Hazard. Mater. 136 (2006) 946-952.
[22] K. Smith, G.A. El-Hiti, Green Chem. 13 (2011) 1579-1608.
[23] V.N. Sheemol, B. Tayagi, R.V. Jasara, J. Mol. Catal. A: Chem. 21 (2004) 201-208.
[24] T. Pinto, P Arquilliere. G. Niccolai, F. Lefebvre, V. Dufaud, New J. Chem. 39 (2015) 5300-5308.
[25] D. Prochazkova, L. Kurfirtova, J. Pavlatova, Catal. Today 179 (2012) 78-84.
[26] P. Gillet, J.M. Malezieux, J.P. Itie, Am. Mineral. 81 (1996) 651-657.
[27] V. Valtchev, G. Majano, S. Mintova, J.P. Ramirez, Chem. Soc. Rev. 42 (2013) 263-290.
[28] L.S. Gadekar, S.S. Katkar, S.R. Mane, B.R. Arbad, M. K. Lande, Bull. Korean Chem. Soc. 30 (2009) 2532-2534.
[29] S.S. Katkar, P.H. Mohite, L.S. Gadekar, B.R. Arbad, M.K. Lande, Green Chem. Lett. Rev. 3 (2010) 287-292.
[30] L.S. Gadekar, B.R. Arbad, M.K. Lande, Bull. Korean Chem. Soc. 30 (2009) 2532-2534.
[31] M.M.J. Treacy, J.B. Higgins, Collection of Simulated XRD Powder Patterns for Zeolites, 5th ed., Amsterdam: Elsevier (2007).
[32] S. Stefanidis, K. Kalogiannis, E.F. Iliopoulou, A.A. Lappas, J. Martínez Triguero, M.T. Navarro, A. Chicab F. Rey, Green Chem. 15 (2013) 1647-1658.
[33] J.N. Kondo, R. Nishitani, E. Yoda, T. Yokoi, T. Tatsumi, K. Domen. Phys. Chem. 12 (2010) 11576-11586.
[34] P.E. Poh, H. Nur, M.N.M. Muhid, H. Hamdan, Catal. Today 114 (2006) 257-262.