References
- (a) Wright, J. B. Chem. Rev. 1951, 48, 397, https://doi.org/10.1021/cr60151a002 . (b) Keri, R. S.; Hiremathad, A.; Budagumpi, S.; Nagaraja, B. M. Chem. Biol. Drug. Des. 2015, 86, 799.
- Grimmett, M. R. Imidazole and Benzimidazole Synthesis; Acadamic Press: San Diego, 1997.
- Figge, A.; Altenbach, H. J.; Brauer, D. J.; Tielmann, P. Tetrahedron Asy. 2002, 13, 137. https://doi.org/10.1016/S0957-4166(02)00079-4
- Kilburn, J. P.; Lau, J.; Jones, R. C. F. Tetrahedron Lett. 2000, 41, 5419. https://doi.org/10.1016/S0040-4039(00)00871-6
- Brain, C. T.; Brunton, S. A. Tetrahedron Lett. 2002, 43, 1893. https://doi.org/10.1016/S0040-4039(02)00132-6
- Wilfred, C. D.; Taylor, R. J. K. Synlett. 2004, 1628.
- Kim, B. H.; Han, R.; Kim, J. S.; Jun, Y. M.; Baik, W.; Lee, B. M. Heterocycles. 2004, 63, 41. https://doi.org/10.3987/COM-03-9903
- Niknam, K.; Fatehi-Raviz, A. J. Iran. Chem. Soc. 2007, 4, 438. https://doi.org/10.1007/BF03247230
- Kumara, R. K.; Punniyamurthy, T. RSC Adv. 2012, 2, 4616. https://doi.org/10.1039/c2ra20328f
- Majumdar, S.; Chakraborty, A.; Bhattacharjee, S.; Debnath, S.; Maiti, D. K. Tetrahedron Lett. 2016, 57, 4595. https://doi.org/10.1016/j.tetlet.2016.08.099
- Yan, Y.-M.; Gao, Y.; Ding, M.-W. Tetrahedron. 2016, 72, 5548. https://doi.org/10.1016/j.tet.2016.07.048
- Shen, M.-G.; Cai, C. J. Fluorine Chem. 2007, 128, 232. https://doi.org/10.1016/j.jfluchem.2007.01.009
- Bahrami, K.; Khodaei, M. M.; Kavianinia, I. Synthesis. 2007, 547. https://doi.org/10.1055/s-2007-965878
- Bahrami, K.; Khodaei, M. M.; Naali, F. Synlett. 2009, 569. https://doi.org/10.1055/s-0028-1087911
- Sadek, K. U.; Al-Qalaf, F.; Mekheimer, R. A.; Elnagdi, M. H. Arab. J. Chem. 2012, 5, 63. https://doi.org/10.1016/j.arabjc.2010.07.024
- Beaulieu, P. L.; Haché, B.; Moos, E. Synthesis. 2003, 1683. https://doi.org/10.1055/s-2003-40888
- Mukhopadhyay, C.; Tapaswi, P. K. Tetrahedron Lett. 2008, 49, 6237. https://doi.org/10.1016/j.tetlet.2008.08.041
- Fazlinia, A.; Mosslemin, M. H.; Sadoughi, H. J. Korean Chem. Soc. 2010, 54, 579. https://doi.org/10.5012/jkcs.2010.54.5.579
- Nagawade, R. R.; Shinde, D. Chin. Chem. Lett. 2006, 17, 453.
- Sharghi, H.; Khalifeh, R.; Mansouri, S. G.; Aberi, M.; Eskandari, M. M. Catal. Lett. 2011, 141, 1845. https://doi.org/10.1007/s10562-011-0671-6
- Sharghi, H.; Hosseini-Sarvari, M.; Moeini, F. Can. J. Chem. 2008, 86, 1044. https://doi.org/10.1139/v08-153
- Li, J.; Bénard, S.; Neuville, L.; Zhu. J. Org. Lett. 2012, 14, 5980. https://doi.org/10.1021/ol3028847
- Peng, J.; Ye, M.; Zong, C.; Hu, F.; Feng, L.; Wang, X.; Wang, Y.; Chen, C. J. Org. Chem. 2011, 76, 716. https://doi.org/10.1021/jo1021426 PMID:21175149
- Kim, Y.; Rajesh Kumar, M.; Park, N.; Heo, Y.; Lee, S. J. Org. Chem. 2011, 76, 9577. https://doi.org/10.1021/jo2019416 PMID:22034860
- Ghashang, M.; Mohammad Shafiee, M. R.; Delzendeh, S.; Fazlinia, A.; Esfandiari, H.; Najafi Biregan, M.; Heydari, N. Bulg. Chem. Commun. 2016, 48, 694.
- Ghashang, M.; Kargar, M.; Mohammad Shafiee, M. R.; Mansoor, S. S.; Fazlinia, A.; Esfandiari, H. Recent Patents Nanotech. 2015, 9, 204. https://doi.org/10.2174/1872210510999151126110657
- Behmaneshfar, A.; Ghashang, M.; Mohammad Shafiee, M. R.; Saffar-Teluri, A.; Fazlinia, A.; Esfandiari, H. Curr. Nanosci. 2015, 11, 56. https://doi.org/10.2174/1573413710666140923211414
- Mohammad Shafiee, M. R.; Mansoor, S. S.; Ghashang, M.; Fazlinia, A. Comptes Rendus Chimie. 2014, 17, 131. https://doi.org/10.1016/j.crci.2013.06.009
- Mohammad Shafiee, M. R.; Ghashang, M.; Fazlinia, A. Curr. Nanosci. 2013, 9, 197. https://doi.org/10.2174/1573413711309020006
- Kumar, D.; Kommi, D. N.; Chebolu, R.; Garg, S. K.; Kumar, R.; Chakraborti, A. K. RSC Adv. 2013, 3, 91. https://doi.org/10.1039/C2RA21994H
- Esfandiari, H.; Jameh-bozorghi, S.; Esmaielzadeh, S.; Shafiee, M. R. M.; Ghashang, M. Res. Chem. Intermed. 2013, 39, 3319. https://doi.org/10.1007/s11164-012-0844-y
- Maddinedi, S. B.; Mandal, B. K. Austin J. Anal. Pharm. Chem. 2014, 1, 1008.