[1] Chughtai A.H., Ahmad N., Younus H.A., Laypkov A., Verpoort F.
Chem. Soc. Rev., 2015,
44:6804
[2] Gascon J., Corma A., Kapteijn F., Llabre´s F.X.
ACS Catal., 2014,
4:361
[3] Dhakshinamoorthy A., Alvaro M., Corma A., Garcia H.
Dalton Trans. 2011,
40:6344
[4] Deria P., Mondloch J.E., Karagiaridi O., Bury W., Hupp J.T., Farha O.K.
Chem. Soc. Rev., 2014,
43:5896
[5] Anumah A., Louis H., Zafar S., Hamzat A., Amusan O., Pigweh A., Akakuru O., Adeleye A., Magu T.,
Chem. Method., 2019,
3:283
[6] Gao S., Zhao N., Shu M., Che S.
Appl. Catal. A: Gen., 2010,
388:196
[7] Nguyen L.T.L., Nguyen C.V., Dang G.H., Le K.K.L., Phan N.T.S.
J. Mol. Catal. A. Chem., 2011,
349:28
[8] Yang J., Li P., Wang L.
Catal. Commun., 2012,
27:58
[9] Li O., Regati S., Butcher R.J., Arman H.D., Chen Z., Xiang S., Chen B., Zhao C.G.
Tetrahedron Lett., 2011,
52:6220
[10] Soleiman-Beigi M., Arzehga Z.
Synlett, 2018,
29:986
[11] Song F., Wang C., Falkowski J.M., Ma L., Lin W.
J. Am. Chem. Soc., 2010,
132:15390
[12] Dhakshina-moorthy A., Alvaro M., Garcia H.
ACS Catal., 2011,
1:48
[13] Puthiaraj P., Suresh P., Pitchumani K.
Green Chem., 2014,
16:2865
[14] Song P., Li Y., Li W., He B., Yang J., Li X.
Int. J. Hydrogen Energy. 2011,
36:10468
[15] Sajjadifar S., Arzehgar Z., Khoshpoori S.
J. Inorg. Organomet. Polym. Mater., 2018,
28:837
[16] Arzehgar Z., Sajjadifar S., Arandiyan H.
Asian J. Green Chem., 2019,
3:43
[17] Soleiman-Beigi M., Arzehgar Z
. J. Sulfur Chem., 2015,
36:395
[18] Soleiman-Beigi M., Arzehgar Z.
Monatsh Chem., 2016,
147:1759
[19] Soleiman‑Beigi M., Arzehgar Z.
Heteroatom Chem., 2015,
26:355
[20] Soleiman-Beigi M., Arzehgar Z., Movassagh B.
Synthesis, 2010,
2010:392
[21] Zhu Z., Lippa B., Drach J.C., Townsend L.B.
J. Med. Chem., 2000,
43:2430
[22] White W., Almassy R., Calvert A.H., Curtin N.J., Griffin R.J., Hostommsky Z., Maegley K., Newell D.R., Srinivasan S., Golding B.T.
J. Med. Chem., 2000,
43:4084
[23] Grimmett M.R.
Imidazole and Benzimidazole Synthesis, Academic Press, San Diego, 1997
[24] Figge A., Altenbach H.J., Brauer D.J., Tielmann P.
Tetrahedron:
Asymmetry, 2002,
13:137
[25] Perry R.J., Wilson B.D.
J. Org. Chem., 1993,
58:7016
[26] Vourloumis D., Takahashi M., Simonsen K.B., Ayida B.K., Barluenga S., Winters G.C., Hermann T.
Tetrahedron Lett., 2003,
44:2807
[27] Venkateswarlu Y., Kumar S.R., Leelavathi P.
Org. Med. Chem. Lett., 2013,
3:7
[28] Yan Z., Zhang W., Gao J., Lin Y., Li J., Lin Z., Zhang L.
RSC Adv., 2015,
5:40094
[29] Trinh N.D., Hong S.S.
J. Nanosci. Nanotechnol., 2015,
15:5450
[30] Doan S.H., Nguyen K.D., Nguyen T.T., Phan N.T.S.
RSC Adv., 2017,
7:1423
[31] Nguyen H.L.
New J. Chem., 2017,
41:14030
[32] Du J.J., Yuan Y.P., Sun J.X., Peng F.M., Jiang X., Qiu L.G., Xie A.J., Shen Y.H., Zhu J.F.
J. Hazard. Mater., 2011,
190:945
[32] Millange F., Guillou N., Medina M.E., Férey G., Carlin-Sinclair A., Golden K.M., Walton R.I.
Chem. Mater., 2010,
22:4237
[33] Fazaeli R., Aliyanb H., Moghadam M., Masoudinia M.
J. Mol. Catal. A: Chem., 2013, 374
[34] Kidwai M. Jahan A., Bhatnagar D.,
J. Chem. Sci., 2010,
122:607
[35] Mohammadi R., Sajjadi A.
J. Med. Chem. Sci., 2019,
2:55
[36] Wang L., Sheng J., Tian H., Qian C.
Syn. Commun., 2004,
34:4265
[37] Rezaee Nezhad E., Tahmasebi R.
Asian J. Green Chem., 2019,
3:34
[38] Fazlini A., Mosslemin M.H., Sadoughi H.
J. Korean Chem. Soc., 2010,
54:579
[39] Kumar J.R., Jawahar J.L., Pathak D.P.
E-J. Chem., 2006,
3:278
[40] Sajjadifar S., Arzehgar Z., Ghayuri A.
J. Chin. Chem. Soc., 2018,
65:205
 as a highly efficient reusable catalyst for the synthesis of 2-aryl-1H-benzimidazole', 'data/chemm/coversheet/251559127758.jpg'))
)