References
- Schneller, S. W. Adv. Heterocycl. Chem. 1975, 18, 59. https://doi.org/10.1016/S0065-2725(08)60128-2
- Rimbault, C. G. U. S. Patent 1989, 4,885,298.
- Choi, E. J.; Lee, J. I.; Kim, G.-H. Int. J. Mol. Med. 2012, 29, 252.
- Engi, H.; Gyemant, N.; Lorand, T.; Levai, A.; Ocsovszki, I.; Molnar, J. In Vivo 2006, 20, 119.
- Zhang, X.; Ma, Z.; Yang, G.; Zheng, Y. Modern Appl. Sci. 2011, 5, 217.
- Robillard, B.; Slaby, H. M.; Lindsay, D. A.; Ingold, K. U. J. Org. Chem. 1986, 51, 1700. https://doi.org/10.1021/jo00360a013
- Dike, S. Y.; Ner, D. H.; Kumar, A. Synlett 1991, 443.
- Aramaki, Y.; Seto, M.; Okawa, T.; Oda, T.; Kanzaki, N.; Shiraishi, M. Chem. Pharm. Bull. 2004, 52, 254. https://doi.org/10.1248/cpb.52.254
- Cui, D.-M.; Kawamura, M.; Shimada, S.; Hayashi, T.; Tanaka, M. Tetrahedron Lett. 2003, 44, 4007. https://doi.org/10.1016/S0040-4039(03)00855-4
- Clayton, S. E.; Gabbutt, C. D.; Hepworth, J. D.; Heron, B. M. Tetrahedron 1993, 49, 939. https://doi.org/10.1016/S0040-4020(01)80335-5
- Konieczny, M. T.; Horowska, B.; Kunikowski, A.; Konopa, J.; Wierzba, K.; Yamada, Y.; Asao, T. J. Org. Chem. 1999, 64, 359. https://doi.org/10.1021/jo980586w
- Sakirolla, R.; Yaeghoobi, M.; Rahman, N. A. Monatsh. Chem. 2012, 143, 797. https://doi.org/10.1007/s00706-011-0663-7
- Kataoka, T.; Watanabe, S.; Mori, E.; Kadomoto, R.; Tanimura, S.; Kohno, M. Bioorg. Med. Chem. 2004, 12, 2397. https://doi.org/10.1016/j.bmc.2004.02.002
- Cordonnier, G.; Rolando, C.; Barbry, D. 9th Int. Electronic Conference on Synth. Org. Chem. 2005, 1-30 Nov, C022.
- Konieczny, W.; Konieczny, M. Synthesis 2009, 1811.
- Ponticello, G. S.; Freedman, M. B.; Habecker, C. N.; Holloway, M. K.; Amato, J. S.; Conn, R. S.; Baldwin, J. J. J. Org. Chem. 1988, 53, 9. https://doi.org/10.1021/jo00236a003
- Bates, D. K.; Li, K. J. Org. Chem. 2002, 67, 8662. https://doi.org/10.1021/jo0259921
- Lee, J. I. Bull. Korean Chem. Soc. 2008, 29, 1263. https://doi.org/10.5012/bkcs.2008.29.6.1263
- Lee, J. I. Bull. Korean Chem. Soc. 2012, 33, 1375. https://doi.org/10.5012/bkcs.2012.33.4.1375
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