[1] H. Schiff, Justus Liebigs Ann. Chem., 1864, 131, 118-119.
[2] Z. Saedi, E. Hoveizi, M. Roushani, S. Massahi, M. Hadian, K. Salehi, J. Mol. Struct., 2019, 1176, 207-216.
[3] C.-H. Dai, F.-L. Mao, J. Struct. Chem., 2013, 54, 624-629.
[4] B.F. Abdel-Wahab, S.F. Mohamed, A.E.G.E. Amr, M.M. Abdalla, Monatsh. Chem., 2008, 139, 1083-1090.
[5] N. Siddiqui, M.A. Bhat, S.A. Khan, W. Ahsan, M.S. Alam, J. Chin. Chem. Soc., 2008, 55, 1326-1331.
[6] M.S. Iorungwa, R.A. Wuana, S.T. Dafa, Chem. Methodol., 2019, 3, 408-424.
[7] P.G. Lacroix. Eur. J. Inorg. Chem., 2001, 2, 339-348.
[8] M.M. Antonijevic, M.B. Petrovic, Int. J. Electrochem. Sci., 2008, 3, 1-28.
[9] I. Sheikhshoaie, S. Davari, S. Ramezanpour, Chem. Methodol., 2018, 2, 47-55.
[10] I. Sheikhshoaie, Z. Tohidiyan, Chem. Methodol., 2019, 3, 30-42.
[11] A. Dehno Khalaji, Chem. Methodol., 2019, 3, 635-643.
[12] I. Sheikhshoaie, M. Sheikhshoaie, S. Ramezanpour, Chem. Methodol., 2018, 2, 103-113.
[13] F. Rahim, F. Malik, H. Ullah, A. Wadood, F. Khan, M.T. Javid, M. Taha, W. Rehman, A. Ur Rehman, K. M. Khan, Bioorg. Chem., 2015, 60, 42-48.
[14] B. Sarikaya, M. Ceruso, F. Carta, C.T. Supuran, Bioorg. Med. Chem., 2014, 22, 5883-5890.
[15] S. Alyar, C. Şen, H. Alyar, Ş. Adem, A. Kalkanci, U.O. Ozdemir, J. Mol. Struct., 2018, 1171, 214-222.
[16] Â. de Fátima, C.D.P. Pereira, C.R.S.D. G. Olímpio, B.G. de Freitas Oliveira, L.L. Franco, P.H.C. da Silva, J. Adv. Res., 2018, 13, 113-126.
[17] M.A. Arafath, F. Adam, F.S.R. Al-Suede, M.R. Razali, M.B.K. Ahamed, A.M.S. Abdul Majid, M.Z. Hassan, H. Osman, S. Abubakar, J. Mol. Struct., 2017, 1149, 216-228.
[18] H.T. Balaydın, M. Özil, M. Şentürk, Arch. Pharm., 2018, 351, art. no. 1800086.
[19] B.L., Liu, Y.X., Wang, Q.X., Liu, R.J. Tao, Z. Naturforsch., 2012, 67b, 192-196.
[20] R. Golbedaghi, A. Salehi, Iran. Chem. Commun., 2018, 6, 78-86.
[21] R. Motamedi, G. Rezanejade Bardajee, S. Shakeri, Iran. Chem. Commun., 2017, 5, 442-448.
[22] T.V. Balashova, R.V. Rumyantsev, G.K. Fukin, A.P. Pushkarev, A.A. Maleev, D.B. Shpakovskii, T.A. Antonenko, E.R. Milaeva, M.N. Bochkarev, Russ. J. Coord. Chem., 2017, 43, 852-857.
[23] R. Golbedaghi, E. Alavipour, Iran. Chem. Commun., 2016, 4, 133-141.
[24] L.N.F. Cardoso, T.C.M. Nogueira, F.A.R. Rodrigues, A.C.A. Oliveira, M.C.S.C. Pessoa, M.V.N. de Souza, Med. Chem. Res., 2017, 26, 1605-1608.
[25] H.M. Gaber, M.C. Bagley, S.M. Sherif, M.A. Sayed, Z. Naturforsch., 2011, 66b, 585-596.
[26] S. Thatha, N. Ummadi, P. Venkatapuram, P. Adivireddy, J. Heterocycl. Chem., 2018, 55, 1410-1418.
[27] P.S. Mahajan, M.D. Nikam, L.U. Nawale, V.M. Khedkar, D. Sarkar, C.H. Gill, ACS Med. Chem. Lett., 2016, 7, 751-756.
[28] M.H. Helal, M.A. Salem, M.A. Gouda, N.S. Ahmed, A.A. El-Sherif, Spectrochim. Acta, Part A, 2015, 147, 73-83.
[29] J. Varshney, A. Sharma, S.P. Gupta, Lett. Drug Des. Discovery, 2012, 9, 389-396.
[30] Y. Kato, N. Hin, N. Maita, A.G. Thomas, S. Kurosawa, C. Rojas, K. Yorita, B.S. Slusher, K. Fukui, T. Tsukamoto, Eur. J. Med. Chem., 2018, 159, 23-34.
[31] K. C. Gulipalli, S. Bodige, P. Ravula, S. Endoori, G. R. Vanaja, G. Suresh Babu, J. N. Narendra Sharath Chandra, N. Seelam, Bioorg. Med. Chem. Lett., 2017, 27, 3558-3564.
[32] M. Fujita, T. Seki, N. Ikeda, Bioorg. Med. Chem. Lett., 2002, 12, 1897-1900.
[33] J. Ivanova, A. Balode, R. Žalubovskis, J. Leitans, A. Kazaks, D. Vullo, K. Tars, C.T. Supuran, Bioorg. Med. Chem., 2017, 25, 857-863.
[34] N.K. Duddukuri, S. Thatikonda, C. Godugu, R.A. Kumar, N. Doijad, ChemistrySelect, 2018, 3, 6859-6864.
[35] Y. Gao, W.-L. Wu, B. Ye, R. Zhou, Y.-L. Wu, Tetrahedron Lett., 1996, 37, 893-896.
[36] Z. Javanshir, S. Jameh-Bozorghi, P. Peyki, Adv. J. Chem. A, 2018, 1, 117-126.
[37] S. Shahab, L. Filippovich, M. Sheikhi, Chem. Methodol., 2017, 1, 159-172.
[38] R. Ahmadi, M.R. Jalali Sarvestani, Iran. Chem. Commun. 2019, 7, 344-351.
[39] M.J. Islam, A. Kumer, N. Sarker, S. Paul, A. Zannat, Adv. J. Chem. A, 2019, 2, 316-326.
[40] M.H. Fekri, A. Omrani, S. Jameh bozorgi, M. Razavi Mehr, Adv. J. Chem. A, 2019, 2, 14-20.
[41] A. Nakhaei, A. Davoodnia, A. Morsali, Russ. J. Phys. Chem. A, 2018, 92, 271-279.
[42] A. Ramazani, M. Sheikhi, H. Yahyaei, Chem. Methodol., 2017, 1, 28-48.
[43] M. Nabati, Chem. Methodol., 2017, 1, 121-135.
[44] W. Saidi, T. Abram, L. Bejjit, M. Bouachrine, Chem. Methodol., 2018, 2, 247-259.
[45] N. Ahmadinejad, M. Talebi Tari, Chem. Methodol., 2019, 3, 55-66.
[46] L. Shiri, D. Sheikh, S. Janinia, M. Sheikhi,
Chem. Methodol., 2019,
3, 392-407.
[47] A. Mirzaie, J. Med. Chem. Sci., 2018, 1, 31-32.
[48] M. Nabati, M. Kermanian, H. Mohammadnejad-Mehrabani, H. Rahbar Kafshboran, M. Mehmannavaz, S. Sarshar, Chem. Methodol., 2018, 2, 128-140.
[49] P. Hosseini, M. Rezaei‒Sameti, Chem. Methodol., 2019, 3, 607-625.
[50] A. Davoodnia, M. Bakavoli, M. Bashash, M. Roshani, R. Zhiani, Turk. J. Chem., 2007, 31, 599-603.
[51] S. Vazirimehr, A. Davoodnia, M. Nakhaei-Moghaddam, N. Tavakoli-Hoseini, Heterocycl. Commun., 2017, 23, 65-70.
[52] N. Dorostkar-Ahmadi, A. Davoodnia, N. Tavakoli-Hoseini, H. Behmadi, Indian J. Heterocycl. Chem., 2018, 28, 543-549.
[53] N. Dorostkar-Ahmadi, A. Davoodnia, N. Tavakoli-Hoseini, H. Behmadi, Z. Naturforsch., 2019, 74b, 175-181.
[54] E. Lammers, J. Nusstein, A. Reader, M. Drum, M. Beck, S. Fowler, J. Endod., 2014, 40, 1287-1292.
[55] M. Frisch, G. Trucks, H. Schlegel, G. Scuseria, M. Robb, J. Cheeseman, J. Montgomery Jr, T. Vreven, K. Kudin, J. Burant. Gaussian 03, revision B. 05; Gaussian, Gaussian 03, revision B. 05; Inc., Pittsburgh, PA, 2003.
[56] R. Ditchfield, Mol. Phys., 1974, 27, 789-807.
[57] R.F. Bader, Chem. Rev., 1991, 91, 893-928.
[58] T.A. Keith, AIMAll (Version 13.05. 06), TK Gristmill Software, Overland Park KS, USA, 2013.
[59] K. Gewald, E. Schinke, H. Bottcher, Chem. Ber., 1966, 99, 94-100.
[60] M. Adib, H. Janatian Ghazvini, M. Soheilizad, S. Saeedi, M. Tajbakhsh, M. Amanlou, Helv. Chim. Acta, 2015, 98, 1079-1086.
[61] I. Rozas, I. Alkorta, J. Elguero, J. Am. Chem. Soc., 2000, 22, 11154-11161.
[62] E. Espinosa, M. Souhassou, H. Lachekar, C. Lecomte, Acta Crystallogr. Sect. B: Struct. Sci., 1999, 55, 563-572.