References
- Chioua, M.; Soriano, E.; Samadi, A.; Marco-Contelles, J. J. Heterocyclic Chem. 2010, 47, 861–872. DOI: 10.1002/jhet.403.
- (a) Panda, N.; Karmakar, S.; Jena, A. K. Chem. Heterocycl. Comp. 2011, 46, 1500–1508. DOI: 10.1007/s10593-011-0699-y. (b) Maqbool, T.; Nazeer, A.; Khan, M. N.; Elliott, M. C.; Khan, M. A.; Ashraf, M.; Nasrullah, M.; Arshad, S.; Munawar, M. A. Asian J. Chem. 2014, 26, 2870–2872. DOI: 10.14233/ajchem.2014.15918. (c) Samar, C.; Ismail, A.; Helmi, T.; Khiari, J.; Bassem, J. J. Bacteriol. Parasitol. 2017, 8, 310–317.
- Quiroga, J.; Villarreal, Y.; Alvez, J. G.; Ortíz, A.; Insuasty, B.; Abonia, R.; Raimondi, M.; Zacchino, S. Chem. Pharm. Bull. 2017, 65, 143–150. DOI: 10.1248/cpb.c16-00652.
- (a) Sindhu, J.; Singh, H.; Khurana, J. M.; Bhardwaj, J. K.; Saraf, P.; Sharma, C. Med. Chem. Res. 2016, 25, 1813–1830. DOI: 10.1007/s00044-016-1604-0. (b) El-Borai, M. A.; Rizk, H. F.; Beltagy, D. M.; El-Deeb, I. Y. Eur. J. Med. Chem. 2013, 66, 415–422. DOI: 10.1016/j.ejmech.2013.04.043. (c) Salem, M. S.; Ali, M. A. M. Biol. Pharm. Bull. 2016, 39, 473–483. DOI: 10.1248/bpb.b15-00586.
- (a) Elneairy, M. A. A.; Eldine, S. M.; Mohamed, A. S. I. Der Pharma Chem. 2015, 7, 284–295. (b) Mohamed, N. R.; Khaireldin, N. Y.; Fahmy, A. F.; El-Sayed, A. A. Der. Pharma. Chem. 2010, 2, 400–417. (c) Rao, H. S. P.; Adigopula, L. N.; Ramadas, K. ACS Comb. Sci. 2017, 19, 279–285. DOI: 10.1021/acscombsci.6b00156.
- Eissa, I. H.; El-Naggar, A. M.; El-Hashash, M. A. Bioorg. Chem. 2016, 67, 43–56. DOI: 10.1016/j.bioorg.2016.05.006.
- (a) Xiaodong, X.; Yongwen, J.; Ma, D. Org. Lett. 2012, 14, 2552–2555. DOI: 10.1021/ol300847v. (b) Gao, M.; Liu, X.; Wang, X.; Cai, Q.; Ding, K. Chin. J. Chem. 2011, 29, 1199–1204. DOI: 10.1002/cjoc.201190223.
- Rui, L.; Yongming, Z.; Liena, Q.; Shunjun, J. Synth. Comm. 2008, 38, 249–254.
- Chandra Sheker Reddy, A.; Narsaiah, B.; Venkataratnam, R. V. J. Fluorine Chem. 1997, 86, 127–130. DOI: 10.1016/0022-1139(96)03412-4.
- (a) Andrés, J. M.; Losada, J.; Maestro, A.; Rodríguez-Ferrer, P.; Pedrosa, R. J. Org. Chem. 2017, 82, 8444–12681. DOI: 10.1021/acs.joc.7b02471. (b) Gunasekaran, P.; Indumathi, S.; Perumal, S. RSC Adv. 2013, 3, 8318–8325. DOI: 10.1039/c3ra00136a.
- (a) Lavecchia, G.; Berteina-Raboin, S.; Guillaumet, G. Tet. Lett. 2004, 45, 2389–2392. DOI: 10.1016/j.tetlet.2004.01.067. (b) El- Emary, T. I. J. Chin. Chem. Soc. 2007, 54, 507–518.; DOI: 10.1002/jccs.200700072. (c) Kendre, D. B.; Toche, R. B.; Jachak, M. N. J. Heterocycl. Chem. 2008, 45, 1281–1286. DOI: 10.1002/jhet.5570450504. (d) Dodiya, D. K.; Trivedi, A. R.; Kataria, V. B.; Shah, V. H. Curr. Org. Chem. 2012, 16, 400–417. DOI: 10.2174/138527212799499912. (e) Ghaedi, A.; Bardajee, G. R.; Mirshokrayi, A.; Mahdavi, M.; Shafiee, A.; Akbarzadeh, T. RSC Adv. 2015, 5, 89652–89658. DOI: 10.1039/C5RA16769H.
- (a) Feng, Q.; Ping, H.; Ruo-Fei, H.; Cheng, X.-H.; Song, W.; Jing, W. Synth. Comm. 2015, 45, 2802–2809. (b) Jie, W.; Niea, B.-J.; Rong, X.-H.; Penga, H.; C. S, W. P. Synlett. 2016, 27, 626–630.
- (a) Li, Y.; Cao, X.; Liu, Y.; Wan, J.-P. Org. Biomol. Chem. 2017, 15, 9585–9589. DOI: 10.1039/c7ob02411h. (b) Li, H.; Xu, X.; Yang, J.; Xie, X.; Huang, H.; Li, Y. Tet. Lett. 2011, 52, 530–533. DOI: 10.1016/j.tetlet.2010.11.106.
- Zhou, P.; Hu, B.; Rao, K.; Li, L.; Yang, J.; Gao, C.; Wang, F.; Yu, F. Synlett. 2018, 29, 519–524. DOI: 10.1055/s-0036-1590950.
- Ashok, K.; Nagaraju, M.; Sirisha, K.; Ganesh Kumar, C.; Krishnaiah, A. Org. Biomol. Chem. 2019, 17, 3186–3194.
- CCDC 1911233 contains the supplementary crystallo graphic data for this paper.
- (a) Muthusaravanan, S.; Sasikumar, C.; Devi Bala, B.; Perumal, S. Green Chem. 2014, 16, 1297–1304. DOI: 10.1039/C3GC42150C. (b) Luo, L.; Meng, L.; Peng, Y.; Xing, Y.; Sun, Q.; Ge, Z.; Li, R. Eur. J. Org. Chem. 2015, 2015, 631–637. DOI: 10.1002/ejoc.201403156.