Spotlight: Use of heterogeneous catalysts in benzimidazole synthesis
Subject Areas : Iranian Journal of Catalysis
1 - Faculty of Chemistry, Shahreza Branch, Islamic Azad University, Shahreza, Isfahan, Iran.
Keywords:
Abstract :
[1] D. Cressier, C. Prouillac, P. Hernandez, C. Amourette, M. Diserbo, C. Lion, G. Rima, Bioorg. Med. Chem. 17 (2009) 5275–5284.
[2] G. Medine, V. Zaikovskii, K.J. Klabunde, J. Mater. Chem. 14 (2004) 757-763.
[3] D. Kee Yi, S. Tamil Selvan, S. Seong Lee, G. Papaefthymiou, D.Kundaliya, J.Ying, J. Mater. Chem. 127 (2005) 4990-4991.
[4] A. Mobini khaledi, M. Zendehdel, S. M. B. Hosseini-Ghazvini, P. Safari, Transition Met. Chem. 40 (2015) 313-320.
[5] J. Lu, H. Fu, J. Org. Chem. 76 (2011) 4600–4605.
[6] H. D. Hanoon, E. Kowsari, M. Abdouss, H. Zandi, M.H. Ghasemi, Res. Chem. Intermed. 43 (2017) 4023-4041.
[7] A. K. Chakraborti, C. Selvam, G. Kaur, S. Bhagat, Synlett. 5 (2004) 851–855.
[8] G. F. Chen, H. M. Jia, L. Y. Zhang, B. H. Chen, J. T. Li, Ultrason. Sonochem. 20 (2013) 627–632.
[9] M. Goravanahalli, B. Raghavendra, Ajjahalli, N. Ramesha, Cigalli, N. Revanna, .Kebbahalli, S. Kanchugarakoppal, Tetrahedron Lett.52 (2011) 5571-5574.
[10] M. Nasr Esfahani, I. Mohammadpoor-Baltork, A. R. Khosropour, M. Moghadam, V. Mirkhani, S. Tangestaninejad, J. Mol. Catal. A: Chem. 379 (2013) 243– 254.
[11] S. M. A. Hakim Siddiki, T. Toyao, K. Shimizu, Green Chem. 20 (2018) 2933–2952.
[12] M. A. Chari, D. Shobha, El-Refaie Kenawy, S. S. Al-Deyab, B.V. S. Reddy, A. Vinu, Tetrahedron Lett. 51 (2010) 5195-5199.
[13] J. Rafique, S. Saba, T. E. A. Frizon, A. L. Braga, ChemistrySelect.3 (2018) 328-334.
[14] H. Alinezhad, F, Salehian. P. Biparva, Synth. Commun. 42 (2012) 102-108.
[15] S. M. Inamdar, V. K. More, S. K. Mandal, Tetrahedron Lett. 54 (2013) 579-583.
[16] M. Jafarpour, A. Rezaeifard, M. Ghahramaninezhad, T. Tabibi, New J Chem. 37 (2013) 2037-2087.
[17] M. Heravi, S. Sadjadi, H. A. Oskooie, R. Shoar, F. Bamoharram, Catal Commun. 9 (2008) 504-507.
[18] R. Fazaeli, H. Aliyan, Appl Catal. 353 (2009) 74-79.
[19] E. Rafiee, N. Rahpeima, S. Eavani Acta Chim Slov. 61 (2014) 177-184.
[20] W. AhmadKhanday, R.Tomar, Catal Commun. 43 (2014) 141-145.
[21] S. Najari, M. Jafarzadeh, K. Bahrami, J. Heterocyclic Chem. 56 (2019) 2853-2856.
[22] R. Kardanpour, S. Tangestaninejad, V. Mirkhani, M. Moghadam, I. Mohammadpoor-Baltork, F. Zadehahmadi, J. Solid State Chem. 253 (2016) 145-153.
[23] K. Wada, H. Yu, Q. Feng, Chin. Chem. Lett. 31 (2020) 605-608.
[24] A. Mobini khaledi, H. Moghanian, S. M. B. Hosseini Ghazvini, A. Dalvand J. Porous Mater. 25 (2018) 1123–1134.
[25] J. Mokhtari, A . Hasani Bozcheloei, Inorg. Chim. Acta, 482 (2018) 726–731.
[26] C. Vallés-García, M. Cabrero-Antonino, S. Navalón, M. Álvaro, A. Dhakshinamoorthy, H. García , J. Colloid Interface Sci. 50 (2020) 885-893.
[27] M. B. Swami, A. H. Jadhav, S. R. Mathpati, H. G. Ghuge, Sudhakar G. Patil, Res. Chem. Intermed. 43 (2017) 2033–2053.
[28] A. Dhakshinamoorthy, K. Kanagaraj, K. Pitchumani, Tetrahedron Lett. 52 (2011) 69–73.
[29] F. Rajabi, S. De, R. Luque, Catal. Lett.145 (2015) 1566–1570.