References
- Lambardino, J. G.; Wiseman, E. H. J. Med .Chem. 1974, 17, 118
- Brimblecombe, R. W.; Duncan, W. A. M.; Durant, G. J.; Emmett, J. C.; Ganellin, C. R.; Parons, M. E. J. Int. Med. Res. 1975, 3, 386
- Tanigawara, Y.; Aoyama, N.; Kita, T.; Shirakawa, K.; Komada, F.; Kasuga, M.; Okumura, K. Clin Pharmacol. Ther. 1999, 66, 528 https://doi.org/10.1016/S0009-9236(99)70017-2
- Heers, J.; Backx, L. J. J.; Mostmans, J. H.; Van Custsem, J. J. Med. Chem. 1979, 22, 1003 https://doi.org/10.1021/jm00194a023
- Wasserscheid, P.; Keim, W. Angew Chem. Int. Ed. 2000, 39, 37872
- Bourissou, D.; Guerret, O.; Ggabbai, F. T.; Bertrand, G. Chem. Rev. 2000, 100
- Satoru, I. Jap. Pat. 1989, 01, 117, 867.
- Satoru, I., Chem. Abstr. 1989, 111, 214482 https://doi.org/10.1002/cber.18820150207
- Radziszewski, B. Chem. Ber. 1882, 15, 1493 https://doi.org/10.1002/cber.18820150207
- Grimmett, M. R. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Pergamon: New York, 1996, 3, 77 https://doi.org/10.1007/s007060070049
- Balalaie, S.; Arabanian, A.; Hashtroudi, M. S. Mont. Fur. Chem. 2000, 131, 945 https://doi.org/10.1007/s007060070049
- Sharam, G. V. M.; Jyothi, Y.; Lakshimi, P. S. Synth. Commun. 2006, 36, 2991 https://doi.org/10.1080/00397910600773825
- Heravi, M. M.; Bakhtiari, K.; Oskooie, H. A.; Taheri, S. J. Mol. Catal. A: Chem. 2007, 263, 279 https://doi.org/10.1016/j.molcata.2006.08.070
- Siddiqui, S. A.; Narkhede, U. G.; Palimkar, S. S.; Daniel, T.; Lahoti, R. J.; Srinivasan, K. V. Tetrahedron 2005, 61, 3539 https://doi.org/10.1016/j.tet.2005.01.116
- Kidwai, M.; Mothsra, P.; Bansal, V.; Goyal, R. Mont. Fur. Chem. 2006, 137, 1189 https://doi.org/10.1007/s00706-006-0518-9
- Sangshetti, J. N.; Kokare, N. D.; Kothakar, S. A.; Shinde, D. B. Mont. Fur. Chem. 2008, 139, 125 https://doi.org/10.1007/s00706-007-0766-3
- Grimmett, M. R. In Comperhensive Hetercyclic Chemistry; Kattritzky, A. R.; Rees, C. W., Eds.; Pergamon: New York, 1984, 5, 457 https://doi.org/10.1021/ol049682b
- Wolkenberg, S. E.; Winoski, D. D.; Leister, W. H.; Wang, Y.; Zhao, Z.; Lindsley, C. W. Org. Lett. 2004, 6, 1453 https://doi.org/10.1021/ol049682b
- Kidwai, M.; Saxena, S.; Ruby.; Rastogi, S. Bull. Korean Chem. Soc. 2005, 26, 2051 https://doi.org/10.5012/bkcs.2005.26.12.2051
- Wang, L. W.; Wang, Y. H.; Tian, H.; Yao, Y. F.; Shao, J. H.; Liu, B. J. Fluorine Chem. 2006, 127, 1570 https://doi.org/10.1016/j.jfluchem.2006.08.005
- Khodaei, M. M.; Bahrami, K.; Kavianinia, I. J. J. Chin. Chem. Soc. 2007, 54, 829 https://doi.org/10.1007/s00706-008-0875-7
- Mohammadi1, A. A.; Mivechi, M.; Kefayati, H. Monatsh Chem. 2008, 139, 935 https://doi.org/10.1007/s00706-008-0875-7
- Sharma, S. D.; Hazarika, P.; Konwar, D. Tetrahedron Letters 2008, 49, 2216 https://doi.org/10.1016/j.tetlet.2008.02.053
- Mizuno, N.; Misono, M. Chem. Rev. 1998, 98, 199 https://doi.org/10.1021/cr960401q
- Notz, W.; Tanaka, F.; Barbas, C. F., III. Acc. Chem. Res. 2004, 37, 580 https://doi.org/10.1021/ar0300468
- Dalko, P. I.; Moisan, L. Angew. Chem, Int. Ed. 2004, 43, 5138 https://doi.org/10.1002/anie.200400650
- Lacoste, E. Synlett 2006, 12, 1973 https://doi.org/10.1016/j.molcata.2006.03.035
- Wang, Y.; Shang, Z. C.; Wu, T. X.; Fan, J. C.;Chen, X. J. Mol. Catal. A: Chem. 2006, 253, 212 https://doi.org/10.1016/j.molcata.2006.03.035
- Srinivasan, M.; Perumal, S.; Selvaraj, S. Arkivoc 2005, xi, 201 https://doi.org/10.1002/adsc.200505144
- Sabitha, G.; Fatima, N.; Reddy, E. V.; Yadav, J. S. Adv. Synth. Catal. 2005, 347, 1353 https://doi.org/10.1002/adsc.200505144
- Dodda, R.; Zhao, C. G. Synthesis 2006, 19, 3238
- Varala, R.; Ramu, E.; Sreelatha, N.; Adapa, S. R. Tetrahedron Lett. 2006, 476, 877 https://doi.org/10.1021/op050129z
- Varala, R.; Adapa, S. R. Org. Proc. Res. Dev. 2005, 9, 853 https://doi.org/10.1021/op050129z
- An, Z.; Zhang, W.: Shi, H.; He, J. Journal of Catalysis 2006, 241, 319-327 https://doi.org/10.1016/j.jcat.2006.04.035
- Karade, N. N.; Budhewar, V. H.; Shinde, S. V.; Jadhav, W. N. Lett. in Org. Chem. 2007, 4, 16 https://doi.org/10.2174/157017807780037405
- Sadaphal, S. A.; Markhele, V. M.; Sonar, S. S.; Shingare, M. S. J. Korean Chemical Soc. 2008, 52, 454 https://doi.org/10.5012/jkcs.2008.52.4.454
- Pawar, S. S.; Dekhane, D. V.; Shingare, M. S.; Thore, S. N. Tetrahedron Lett. 2008, 49, 4252 https://doi.org/10.1016/j.tetlet.2008.04.148
- Sadaphal, S. A.; Shelke, K. F.; Sonar, S. S.; Shingare, M. S. Central Euro. J. Chem. 2008, 6, 622 https://doi.org/10.2478/s11532-008-0069-5
- Sonar, S. S.; Kategaonkar, A. H.; Ware, M. N.; Gill, C. H.; Shingate, B. B.; Shingare, M. S. Arkivoc 2009, ii, 138
- Shelke, K. F.; Sapkal, S. B.; Sonar, S. S.; Madje, B. R.; Shingate, B. B.; Shingare, M. S. Bull. Korean Chem. Soc. 2009, 30, 1057 https://doi.org/10.1021/jo050186q
- Li, G. I.; Zhao, G. J. Org. Chem. 2005, 70, 4272 https://doi.org/10.1021/jo050186q
- Borah, B. M.; Das, G. Tetrahedron Lett. 2006, 47, 3135 https://doi.org/10.1016/j.tetlet.2006.02.137
- Yanagisawa, A.; Nakamura, Y.; Arai, T. Tetrahedron: Asymmetry 2004, 15, 1909 https://doi.org/10.1016/j.tetasy.2004.04.036
- Varala, R.; Nasreen, A.; Enugala, R.; Adapa, S. R. Tetrahedron Lett. 2007, 48, 69 https://doi.org/10.1016/j.tetlet.2006.11.010
- Bahmanyar, S.; Houk, K. N.; Matin, H. J.; List, B. J. Am. Chem. Soc. 2003, 125, 2475 https://doi.org/10.1021/ja028812d
- Arno, M.; Domingo, L. R. Theor. Chem. Acc. 2002, 108, 232 https://doi.org/10.1021/ja011714s
- Bahmanyar, S.; Houk, K. N. J. Am. Chem. Soc. 2001, 123, 12911 https://doi.org/10.1021/ja011714s
- Bahmanyar, S.; Houk, K. N. J. Am. Chem. Soc. 2001, 123, 11273 https://doi.org/10.1021/ja011403h
- Grogee, H.; Wilken, J. Angew. Chew. Int. Ed. 2001, 40, 529 https://doi.org/10.1002/1521-3773(20010202)40:3<529::AID-ANIE529>3.0.CO;2-X
- List, B.; Pojarliev, P.; Castello, C. Org. Lett. 2001, 3, 573 https://doi.org/10.1021/ol006976y
- Sharma, S. D.; Hazarika, P.; Konwar, D. Tetrahedron Lett. 2008, 49, 2216 https://doi.org/10.1016/j.tetlet.2008.02.053
Cited by
- New approach to the multicomponent one-pot synthesis of 2-aryl-1H-phenanthro[9,10-d]imidazoles vol.17, pp.1-2, 2011, https://doi.org/10.1515/hc.2011.018
- Ammonium metavanadate as an efficient catalyst for the synthesis of 2,4,5-triaryl-1H-imidazoles vol.48, pp.3, 2011, https://doi.org/10.1002/jhet.548
- Micron-particulate crystalline hexagonal aluminium nitride: a novel, efficient and versatile heterogeneous catalyst for the synthesis of some heterocyclic compounds vol.10, pp.2, 2013, https://doi.org/10.1007/s13738-012-0152-x
- Brønsted acid ionic liquid [Et3NH][HSO4] as an efficient and reusable catalyst for the synthesis of 2,4,5-triaryl-1H-imidazoles vol.39, pp.3, 2013, https://doi.org/10.1007/s11164-012-0669-8
- , AN EFFICIENT AND RECYCLABLE CATALYST vol.43, pp.2, 2013, https://doi.org/10.1080/10826068.2012.719845
- ChemInform Abstract: L-Proline as an Efficient Catalyst for the Synthesis of 2,4,5-Triaryl-1H-imidazoles. vol.41, pp.7, 2010, https://doi.org/10.1002/chin.201007106
- Sulfated Tin Oxide: A Reusable and Highly Efficient Heterogeneous Catalyst for the Synthesis of 2,4,5-Triaryl-1H-imidazole Derivatives vol.42, pp.10, 2009, https://doi.org/10.1080/00397911.2010.541744