References
- Li, S. M. Nat. Prod. Rep. 2010, 27, 57. https://doi.org/10.1039/b909987p
- Weng, J. R.; Tsai, C. H.; Kulp, S. K.; Chen, C. S. Cancer Lett. 2008, 262, 153. https://doi.org/10.1016/j.canlet.2008.01.033
- Rieck, G. C.; Fiander, A. N. Mol. Nutr. Food Res. 2008, 52, 105. https://doi.org/10.1002/mnfr.200700138
- Brancale, A.; Silvestri, R. Med. Res. Rev. 2007, 27, 209. https://doi.org/10.1002/med.20080
- Somei, M.; Yamada, F. Nat. Prod. Rep. 2005, 22, 73. https://doi.org/10.1039/b316241a
- McKay, M. J.; Carroll, A. R.; Quinn, R. J.; Hooper, J. N. A. J. Nat. Prod. 2002, 65, 595. https://doi.org/10.1021/np010347v
- Joule, J. A.; Mills, K. Heterocyclic Chemistry, 4th ed.; Blackwell Science; Oxford, 2000.
- Sundberg, R. J. Indoles; Academic Press: London, 1996.
- Ishikura, M.; Yamada, K. Nat. Prod. Rep. 2009, 26, 803. https://doi.org/10.1039/b820693g
- Higuchi, K.; Kawasaki, T. Nat. Prod. Rep. 2007, 24, 843. https://doi.org/10.1039/b516351j
- Kawasaki, T.; Higuchi, K. Nat. Prod. Rep. 2005, 22, 761. https://doi.org/10.1039/b502162f
- Walker, S. R.; Carter, E. J.; Huff, B. C.; Morris, J. C. Chem. Rev. 2009, 109, 3080. https://doi.org/10.1021/cr900032s
- Leblanc, Y.; Black, W. C.; Chan, C. C.; Charleson, S.; Delorme, D.; Denis, D.; Bayly, C.; Gauthier, J.Y.; Grimm, R.; Gordon, R.; Guay, D.; Hamel, P.; Kargman, S.; Lau, C. K.; Mancini, J.; Ouellet, M.; Percival, D.; Roy, P.; Skorey, K.; Tagari, P.; Vickers, P.; Wong, E.; Xu, L.; Prasit, P. Bioorg. Med. Chem. Lett. 1996, 6, 731. https://doi.org/10.1016/0960-894X(96)00101-1
- Pawlak, J. M.; Khau, V. V.; Hutchinson, D. R.; Martinelli, M. J. Org. Chem. 1996, 61, 9055. https://doi.org/10.1021/jo9614452
- Shefali, S.; Srivastava, S. K.; Husbands, S. M.; Lewis, J. W. J. Med. Chem. 2005, 48, 635. https://doi.org/10.1021/jm040853s
- Landwehr, J.; George, S.; Karg, E. M.; Poeckel, D.; Steinhilber, D.; Troschuetz, R.; Werz, O. J. Med. Chem. 2006, 49, 4327. https://doi.org/10.1021/jm050801i
- Karg, E. M.; Luderer, S.; Pergola, C.; Buhring, U.; Rossi, A.; Northoff, H.; Sautebin, L.; Troschutz, R.; Werz, O. J. Med. Chem. 2009, 52, 3474. https://doi.org/10.1021/jm900212y
- Kevin, H.; Aurelien, G. J. C.; Shengze, Z.; John, A. M. Tetrahedron Lett. 2009, 50, 3290. https://doi.org/10.1016/j.tetlet.2009.02.060
- Goh, W. K.; Black, D. C.; Kumar, N. Tetrahedron Lett. 2007, 48, 9008. https://doi.org/10.1016/j.tetlet.2007.10.093
- Dalpozzo, R.; Bartoli, G. Curr. Org. Chem. 2005, 9, 163. https://doi.org/10.2174/1385272053369204
- Chintakunta, R.; Verrababurao, K.; Raju, B. R.; Kuo, C.; Yao, C. F. Tetrahedron Lett. 2009, 50, 4037. https://doi.org/10.1016/j.tetlet.2009.04.064
- Ghanamani, S.; Paramasivan, T. P. Tetrahedron Lett. 2009, 50, 3959. https://doi.org/10.1016/j.tetlet.2009.04.089
- Gribble, G. W. J. Chem. Soc., Perkin Trans. 1 2000, 1045.
- Humphrey, G. R.; Kuethe, J. T. Chem. Rev. 2006, 106, 2875. https://doi.org/10.1021/cr0505270
- Candeias, N. R.; Branco, L. C.; Gois, P. M. P.; Afonso, C. A. M.; Trindade, A. F. Chem. Rev. 2009, 109, 2703. https://doi.org/10.1021/cr800462w
- Nenitzescu, C. Chem. Zentralbl. 1929, 2331.
- Parr, R. W.; Reiss, J. A. Aust. J. Chem. 1984, 37, 1263. https://doi.org/10.1071/CH9841263
- Pawlak, J. M.; Khau, V. V.; Hutchison, D. R.; Martinelli, M. J. J. Org. Chem, 1996, 61, 9055. https://doi.org/10.1021/jo9614452
- Ketcha, D. M.; Wilson, L. J.; Portlock, D. E. Tetrahedron Lett. 2000, 41, 6253. https://doi.org/10.1016/S0040-4039(00)00697-3
- Neumann, J. J.; Rakshit, S.; Drcge, T.; Wurtz, S.; Glorius, F. Chem. Eur. J. 2011, 17, 7298. https://doi.org/10.1002/chem.201100631
- Clark, J. H. Acc. Chem. Res. 2002, 35, 791. https://doi.org/10.1021/ar010072a
- Balogh, M.; Laszlo, P. In Organic Chemistry Using Clay; Spinger-Verlag: New York, 1993.
- Laszlo, P. Science 1987, 235, 1473. https://doi.org/10.1126/science.235.4795.1473
- Laszlo, P. Pure Appl. Chem. 1990, 62, 2027. https://doi.org/10.1351/pac199062102027
- Cornelis, A.; Laszlo, P. Synlett 1994, 155.
- Yadav, J. S.; Reddy, B. V. S.; Sunitha, V.; Reddy, K. S.; Ramakrishna, K. V. S. Tetrahedron Lett. 2004, 45, 7947. https://doi.org/10.1016/j.tetlet.2004.08.128
- Yadav, J. S.; Reddy, B. V. S.; Satheesh, G. Tetrahedron Lett. 2004, 45, 3673. https://doi.org/10.1016/j.tetlet.2004.03.039
- Yadav, J. S.; Reddy, B. V. S.; Sadasiv, K.; Reddy, P. S. R. Tetrahedron Lett. 2002, 43, 3853. https://doi.org/10.1016/S0040-4039(02)00679-2
- Yadav, J. S.; Reddy, B. V. S.; Kumar, G. M.; Murthy, Ch. V. S. R. Tetrahedron Lett. 2001, 42, 89. https://doi.org/10.1016/S0040-4039(00)01891-8
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