References
- Tietze, L. F.; Brasche, G.; Gericke, K. M. Domino Reactions in Organic Synthesis; WILEY-VCH Verlag GmbH & Co. KGaA: Weinheim, 2006.
- Zhu, J.; Bienayme, H. Multicomponent Reactions; Wiley: Weinheim, 2005.
- Barry, B. T.; Dennis, G. H. Chem. Rev. 2009, 109, 4439. https://doi.org/10.1021/cr800296p
- Magedov, I. V.; Manpadi, M.; Ogasawara, M. A.; Dhawan, A. S.; Rogelj, S.; Van slambrouck, S.; Steelant, W. F. A.; Evdokimov, N. M.; Uglinskii, P. Y.; Elias, E. M.; Knee, E. J.; Tongwa, P.; Antipin, M. Y.; Kornienko, A. J. Med. Chem. 2008, 51, 2561. https://doi.org/10.1021/jm701499n
- Mukhopadhyay, M.; Bhatia, B.; Iqbal, J. Tetrahedron Lett. 1997, 38, 1083. https://doi.org/10.1016/S0040-4039(96)02474-4
- Barluenga, J.; Viado, A. L.; Aguilar, E.; Fustero, S.; Olano, B. J. Org. Chem. 1993, 58, 5972. https://doi.org/10.1021/jo00074a024
- Enders, D.; Moser, M.; Geibel, G.; Laufer, M. C. Synthesis 2004, 2040.
- Kobinata, K.; Uramoto, M.; Nishii, M.; Kusakabe, H.; Nakamura, G.; Isono, K. Agric. Biol. Chem. 1980, 44, 1709 https://doi.org/10.1271/bbb1961.44.1709
- Fiedler, E.; Fiedler, H.-P.; Gerhard, A.; Keller-Schierlein, W.; Koenig, W. A.; Zaehner, H. Arch. Microbiol. 1976, 107, 249. https://doi.org/10.1007/BF00425335
- Jeffs, P. W.; Redfearn, R.; Wolffram, J. J. Org. Chem. 1983, 48, 3861. https://doi.org/10.1021/jo00169a068
- Dallemagne, P.; Rault, S.; Severicourt, M.; Hassan, K. M.; Robba, M. Tetrahedron Lett. 1986, 27, 2607. https://doi.org/10.1016/S0040-4039(00)84596-7
- Paleo, M. R.; Dominguez, D.; Castedo, L. Tetrahedron Lett. 1993, 34, 2369. https://doi.org/10.1016/S0040-4039(00)77616-7
- Dakin, H. D.; West, R. J. Biol. Chem. 1928, 78, 745.
- Buchanan, G. L. Chem. Soc. Rev. 1988, 17, 91. https://doi.org/10.1039/cs9881700091
- Rao, I. N.; Prabhakaran, E. N.; Das, S. K.; Iqbal, J. J Org. Chem. 2003, 68, 4079. https://doi.org/10.1021/jo020559c
- Khan, A. T.; Parvin, T.; Choudhury, L. H. Tetrahedron 2007, 63, 5593. https://doi.org/10.1016/j.tet.2007.04.019
- Khan, A. T.; Choudhury, L. H.; Parvin, T.; Ali, A. Tetrahedron Lett. 2006, 47, 8137. https://doi.org/10.1016/j.tetlet.2006.09.041
- Pandey, G.; Singh, R. P.; Garg, A.; Singh, V. K. Tetrahedron Lett. 2005, 46, 2137. https://doi.org/10.1016/j.tetlet.2005.01.118
- Ghosh, R.; Maiti, S.; Chakraborty, A.; Chakraborty, S.; Mukherjee, A. K. Tetrahedron 2006, 62, 4059. https://doi.org/10.1016/j.tet.2006.02.037
- Hassankhani, A.; Maghsoodlou, M. T.; Habibi-Khorassani, S. M.; Hosseini-Mahdiabad, H.; Marandi, G. ARKIVOC 2008, (ii), 134.
- Shaterian, H. R.; Yarahmadi, H.; Ghashang, M. ARKIVOC 2007, (xvi), 298.
- Khodaei, M. M.; Khosropour, A. R.; Fattahpour, P. Tetrahedron Lett. 2005, 46, 2105. https://doi.org/10.1016/j.tetlet.2005.01.149
- Rafiee, E.; Shahbazi, F.; Joshaghani, M.; Tork, F. J. Mol. Catal. A: Chem. 2005, 242, 129. https://doi.org/10.1016/j.molcata.2005.08.005
- Bahulayan, D.; Das, S. K.; Iqbal, J. J. Org. Chem. 2003, 68, 5735. https://doi.org/10.1021/jo020734p
- Das, B.; Reddy, K. R. Helv. Chim. Act. 2006, 89, 3109. https://doi.org/10.1002/hlca.200690279
- Harmata, M., Ed.; Silver in Organic Chemistry; John Wiley & Sons Inc.: Hoboken, 2010.
- Tschan, M. J.-L.; Thomas, C. M.; Strub, H.; Carpentier, J.-F. Adv. Synth. Catal. 2009, 351, 2496. https://doi.org/10.1002/adsc.200800750
- Rosenfeld, D. C.; Shekhar, S.; Takemiya, A.; Utsunomiya, M.; hartwig, J. F. Org. Lett. 2006, 8, 4179. https://doi.org/10.1021/ol061174+
- Shinu, V. S.; Sheeja, B.; Purushothaman, E., Bahulayan, D. Tetrahedron Lett. 2009, 50, 4838. https://doi.org/10.1016/j.tetlet.2009.06.022
Cited by
- An Efficient and Environmentally Friendly Procedure for the Synthesis of Some Novel 8-Benzylidene-4-phenyl-3,4,5,6,7,8-hexahydro-1H-quinazolin-2-ones/thiones using Tetrabutylammonium Hexatungstate as a Reusable Heterogeneous Catalyst under Solvent-Free Conditions vol.34, pp.11, 2013, https://doi.org/10.5012/bkcs.2013.34.11.3289
- Recent Advances and Perspectives in the Silver-catalyzed Multi-component Reactions vol.24, pp.None, 2012, https://doi.org/10.2174/1385272824666200217102036