References
- Denny, W. A.; Revacastle, G. W.; Baguley, B. J. Med. Chem. 1990, 33, 814. https://doi.org/10.1021/jm00164a054
- Israel, M.; Day, A. R. J. Org. Chem. 1959, 24, 1455. https://doi.org/10.1021/jo01092a018
- Kassidy, P. E. Thermally Stable Polymers; Marcell Dekkar: New York, 1980.
- Yildiz, I. O.; Yalcin, I.; Akisener, E.; Ucarturk, N. Eur. J. Med. Chem. 2004, 39, 291. https://doi.org/10.1016/j.ejmech.2003.11.014
- Song, X.; Vig, B. S.; Lorenzi, P. L.; Drach, J. C.; Townsend, L. B.; Amidon, G. L. J. Med. Chem. 2005, 48, 1274. https://doi.org/10.1021/jm049450i
- Yamato, M. J. Pharm. Soc. Jpn. 1992, 112, 81.
- Kumar, D.; Jacob, M. R.; Reynolds, M. B.; Karvin, S. M. Bioorg. Med. Chem. 2002, 10, 3997. https://doi.org/10.1016/S0968-0896(02)00327-9
- Benazzouz, A.; Boraud, T.; Dubedat, P.; Boireau, A.; Stutzmann, J. M.; Gross, C. Eur. J. Pharmacol. 1995, 284, 299. https://doi.org/10.1016/0014-2999(95)00362-O
- Grimmett, M. R.; Katritzky, A. R.; Rees, C. W.; Sceiven, E. F. V.; Comprehensive Heterocyclic Chemistry II, Vol 3; Elsevier Science Ltd: Oxford, 1996.
- Alcalde, E.; Dinares, I.; Perez-Garcia, L.; Roca, T. Synthesis 1992, 395.
- Pottorf, R. S.; Chadha, N. K.; Katkevics, M.; Ozola, V.; Suna, E.; Ghane, H.; Regberg, T.; Player, M. R. Tetrahedron Lett. 2003, 44, 175. https://doi.org/10.1016/S0040-4039(02)02495-4
- Nadaf, R. N.; Siddiqui, S. A.; Daniel, T.; Lahoti, R. J.; Srinivasan, K. V. J. Mol. Catal. A: Chem. 2004, 214, 155. https://doi.org/10.1016/j.molcata.2003.10.064
- Jenkins, G. L.; Knevel, A. M.; Davis, C. S. J. Org. Chem. 1961, 26, 274.
- Doise, M.; Dennin, F.; Blondeau, D.; Sliwa, H. Tetrahetron Lett. 1990, 31, 1155. https://doi.org/10.1016/S0040-4039(00)88750-X
- Villemin, D.; Hammadi, M; Martin, B. Synthetic Commun. 1996, 26, 2895. https://doi.org/10.1080/00397919608005224
- Chakraborti, A. K.; Rudrawar, S.; Kaur, G.; Sharma, L. Synlett 2004, 1533.
- Hari, A.; Karan, C.; Rodridues, W. C.; Miller, B. L. J. Org. Chem. 2001, 66, 991. https://doi.org/10.1021/jo005758f
- Beaulieu, P. L.; Hache, B.; Von Moss, E. Synthesis 2003, 1683.
- Curini, M.; Epifano, F.; Montanari, F.; Rosati, O.; Taccone, S. Synlett 2004, 1832.
- Gogoi, P.; Konwar, D. Tetrahedron Lett. 2006, 47, 79. https://doi.org/10.1016/j.tetlet.2005.10.134
- Trivedi, R.; De, S. K.; Gibbs, R. A. J. Mol. Catal. A: Chem. 2006, 245, 8. https://doi.org/10.1016/j.molcata.2005.09.025
- Navarrete-Vazquez, G.; Moreno-Diaz, H.; Aguirre-Crespo, F.; Leon-Revara, I.; Villalobos-Molina, R.; Munoz-Muniz, O.; Estrada-Soto, S. Bioorg. Med. Chem. Lett. 2006, 16, 4169. https://doi.org/10.1016/j.bmcl.2006.05.082
- Boyd, G. V.; Katritzky, A. R.; Rees, C. W.; Potts, K. T. Comprehensive Heterocyclic Chemistry; Pregamon Press: New York, 1984; p 177.
- Bu, X. Z.; Huang, Z. S.; Zhang, M.; Ma, L.; Xiao, G. W.; Gu, L. Q. Tetrahedron Lett. 2001, 42, 5737. https://doi.org/10.1016/S0040-4039(01)01034-6
- Bhaval, B. M.; Mayabhate, S. P.; Likhite, A. P.; Deshmukh, A. R. A. S. Synthetic Commun. 1995, 25, 3315. https://doi.org/10.1080/00397919508013850
- Tundo, D.; Anastas, P. T.; Green Chemistry: Theory and Practice; Oxford University Press: Oxford, 1998.
- Toda, F. Acc. Chem. Res. 1995, 28, 480. https://doi.org/10.1021/ar00060a003
- Chakraborti, A. K.; Gulhane, R. Chem. Commun. 2003, 1896.
- Hajipoor, A. R.; Abidi, H.; Rooho, A. E. J. Org. Chem. 2003, 68, 4553. https://doi.org/10.1021/jo034217y
- Bandgar, B. P.; Patil, A. V.; Kamble, V. T. Arkivoc 2007, 16, 252.
- Bandgar, B. P.; Patil, A. V.; Kamble, V. T.; Totre, J. V. J. Mol. Catal. A: Chem. 2007, 273, 114. https://doi.org/10.1016/j.molcata.2007.02.051
- Bandgar, B. P.; Patil, A. V.; Kamble, V. T.; Chavan, O. S. Cat. Commun. 2007, 8, 1065. https://doi.org/10.1016/j.catcom.2006.10.003
- Bandgar, B. P.; Patil, A. V.; Chavan, O. S. J. Mol. Catal. A: Chem. 2006, 256, 99. https://doi.org/10.1016/j.molcata.2006.04.024
- Raban, M.; Chang, H.; Craine, L.; Hortelano, E. J. Org. Chem. 1985, 50, 2205. https://doi.org/10.1021/jo00213a001
- Wang, H.; Partch, R. E.; Li, Y. J. Org. Chem. 1997, 62, 5222. https://doi.org/10.1021/jo970253j
- Wang, L.; Sheng, J.; Tian, H.; Qian, C. Synthetic Commun. 2004, 34, 4265. https://doi.org/10.1081/SCC-200039340
- Joshi, A. A.; Vishwanathan, C. L. Bioorg. Med. Chem. Lett. 2006, 16, 2613. https://doi.org/10.1016/j.bmcl.2006.02.038
- Kumar, D.; David, W. M.; Kervin, S. M. Bioorg. Med. Chem. Lett. 2001, 11, 2971. https://doi.org/10.1016/S0960-894X(01)00606-0
- Heravi, M. M.; Montazeri, N.; Rahmizadeh, M.; Bakavoli, M.; Ghassemzadeh, M. J. Chem. Res. (S) 2000, 584.
Cited by
- Synthetic approaches to imidazo[4,5-b]pyridine derivatives (review) vol.47, pp.5, 2011, https://doi.org/10.1007/s10593-011-0797-x
- Functionalized Orthoesters as Powerful Building Blocks for the Efficient Preparation of Heteroaromatic Bicycles vol.14, pp.13, 2012, https://doi.org/10.1021/ol301472a
- Iron Sulfide Catalyzed Redox/Condensation Cascade Reaction between 2-Amino/Hydroxy Nitrobenzenes and Activated Methyl Groups: A Straightforward Atom Economical Approach to 2-Hetaryl-benzimidazoles and -benzoxazoles vol.135, pp.1, 2013, https://doi.org/10.1021/ja311780a
- A Simple, Efficient Synthesis of 2-Aryl Benzimidazoles Using Silica Supported Periodic Acid Catalyst and Evaluation of Anticancer Activity vol.2013, pp.2090-5157, 2013, https://doi.org/10.1155/2013/453682
- -Substituted Anilines and Orthoesters vol.45, pp.1, 2013, https://doi.org/10.1080/00304948.2013.743751
- Facile synthesis of benzimidazole, benzoxazole, and benzothiazole derivatives catalyzed by sulfonated rice husk ash (RHA-SO3H) as an efficient solid acid catalyst vol.41, pp.8, 2015, https://doi.org/10.1007/s11164-014-1685-7
- nanocomposite; synthesis, characterization and its application as a novel and recyclable catalyst for the one-pot synthesis of benzoxazole derivatives in aqueous media vol.5, pp.58, 2015, https://doi.org/10.1039/C5RA06618B
- ′-diarylformamidines, benzoxazoles, benzothiazoles and benzimidazoles vol.42, pp.8, 2018, https://doi.org/10.1039/C8NJ00171E
- Synthesis and Pharmacological Investigations of Novel Pyrazolyl and Hydrazonoyl Cyanide Benzimidazole Entities pp.0022152X, 2019, https://doi.org/10.1002/jhet.3522
- Periodic Mesoporous Organosilica Containing Bridged N ‐Sulfonic Acid Groups: Promotion of the Synthesis of N,N’‐ Diarylformamidines, Benzoxazoles, Benzothiazoles and Benzimidazoles vol.4, pp.27, 2019, https://doi.org/10.1002/slct.201900885
- Synthesis of new azo‐dispersive dyes with benzo[d]imidazole moiety and new bis benzo[d]imidazoles using DABCO‐diacetate as a green media vol.68, pp.4, 2021, https://doi.org/10.1002/jccs.202000378
- Solid‐Supported Materials‐Based Synthesis of 2‐Substituted Benzothiazoles: Recent Developments and Sanguine Future vol.6, pp.25, 2010, https://doi.org/10.1002/slct.202101368
- Benzothiazoles from Condensation of o-Aminothiophenoles with Carboxylic Acids and Their Derivatives: A Review vol.26, pp.21, 2010, https://doi.org/10.3390/molecules26216518