References
- F. Hobrecker, “Ueber Reductionsprodukte Der Nitracetamidverbindungen,” Berichte Der Deutschen Chemischen Gesellschaft 5, no. 2 (1872): 920–924.
- A. Ladenburg, “Derivate Von Diaminen,” Berichte Der Deutschen Chemischen Gesellschaft 8, no. 1 (1875): 677–678.
- A. R. Day, Electronic Mechanisms of Organic Reactions (New York: American Book Company, 1950), 242–243.
- S. K. Kumar, A. L. Rao, A. Prameela Rani, G. N. V. Mounika, and J. S. Ramya, “Aluminium Chloride Catalyzed One Pot Synthesis of 2 Aryl Substituted Benzimidazoles and Their Antibacterial Activity,” IJPP 4, no. 4 (2017): 198–202.
- J. B. Wright, The chemistry of the benzimidazoles, 1951. 522–523.
- W. A. Denny, G. W. Rewcastle, and B. C. Baguley, “Potential Antitumor Agents. 59. Structure–Activity Relationships for 2-Phenylbenzimidazole-4-Carboxamides, A New Class of "Minimal" DNA-Intercalating Agents Which May Not Act via Topoisomerase II,” Journal of Medicinal Chemistry 33, no. 2 (1990): 814–819.
- T. Fonseca, B. Gigante, and T. Gilchrist, “A Short Synthesis of Phenanthro[2,3-d]Imidazoles from Dehydroabietic Acid. Application of the Methodology as a Convenient Route to Benzimidazoles,” Tetrahedron 57, no. 9 (2001): 1793–1799.
- M. Sun, X. Wu, J. Chen, J. Cai, M. Cao, and M. Ji, “Design, Synthesis, and In Vitro Antitumor Evaluation of Novel Diaryl Ureas Derivatives,” European Journal of Medicinal Chemistry 45, no. 6 (2010): 2299–2309.
- D. Carcanague, Y. K. Shue, M. A. Wuonola, M. Uria-Nickelsen, C. Joubran, J. K. Abedi, J. Jones, and T. C. Kuehler, “Novel Structures Derived from 2-[[(2-Pyridyl)Methyl]Thio]-1H-Benzimidazole as Anti-Helicobacter Pylori Agents, Part 2,” Journal of Medicinal Chemistry 45, no. 19 (2002): 4300–4309.
- M. Lezcano, W. Al-Soufi, M. Novo, E. Rodriguez-Nunez, and J. V. Tato, “Complexation of Several Benzimidazole-Type Fungicides with Alpha- and Beta-Cyclodextrins,” Journal of Agricultural and Food Chemistry 50, no. 1 (2002): 108 1
- A. K. Tewari, and A. Mishra, “Synthesis and Antiviral Activities of N-Substituted-2-Substituted-Benzimidazole Derivatives.” Indian Journal of Chemistry 45 (2006): 489–493.
- M. Curini, F. Epifano, F. Montanari, O. Rosati, and S. Taccone, “Ytterbium Triflate Promoted Syntheis of Benzimidazole Derivaitves,” Synlett 2004, no. 10 (2004): 1832–1834.
- P. Gogoi, and D. Konwar, “An Efficient and One Pot Synthesis of Imidazoline and Benzimidazole via Anaerobic Oxidation of C-N Bonds in Water,” Tetrahedron Letters 47 (2006): 49.
- K. R. Hornberger, G. M. Adjabeng, H. D. Dickson, and R. G. DAvis-Ward, “A Mild One Pot Synthesis of Disubstitued Benzimidazoles from 2-Nitroanilines,” Tetrahedron Letters 47, no. 30 (2006): 5359–5361.
- U. Srinivas, C. Srinivas, P. Narender, V. J. Rao, and S. Palaniappan, “Polyaniline-Sulfate Salt as an Efficient and Reusable Catalyst for the Synthesis of 1,5-Benzodiazepines and 2-Phenyl Benzimidazoles,” Catalysis Communications 8, no. 1 (2007): 107–110.