References
- Tanaka, H.; Tanaka, T.; Etoh, H.; Goto, S.; Terada, Y. Heterocycles1999, 51, 2759-2764. https://doi.org/10.3987/COM-99-8686
- Dyke, S. F.; Quessy, S. N. The Alkaloids; Rodrigo, R. G. A., Ed.; Academic Press: New York, 1981; Vol. 18.
- Miranda, L. D.; Zard, S. Z. Org. Lett. 2002, 4, 1135-1138. https://doi.org/10.1021/ol025534e
- Chikaoka, S.; Toyao, A.; Ogasawara, M.; Tamura, O.; Ishibashi H. J. Org. Chem. 2003, 68, 312-318 https://doi.org/10.1021/jo020573p
- Allin, S. M.; Streetley, G. B.; Slater, M.; James, S. L.; Martin, W. P. Tetrahedron Lett. 2004, 45, 5493-5496. https://doi.org/10.1016/j.tetlet.2004.05.060
- Allin, S. M.; James, S. L.; Elsegood, M. R. J.; Martin, W. P. J. Org. Chem. 2002,67, 9464-9467. https://doi.org/10.1021/jo0205661
- Padwa, A.; Lee, H. I.; Rashatasakhon, P.; Rose, M. J. Org. Chem. 2004, 69, 8209-8218 https://doi.org/10.1021/jo048647f
- Katritzky, R. A.; He, H.-Y.; Jiang, R. Tetrahedron Lett. 2002, 43,2831-2833. https://doi.org/10.1016/S0040-4039(02)00350-7
- Rigby, J. H.; Hughes, R. C.; Heeg, M. J. J. Am. Chem. Soc.1995, 117, 7834-7835. https://doi.org/10.1021/ja00134a040
- Rigby, J. H.; Deur, C.; Heeg, M. J. Tetrahedron Lett. 1999, 40, 6887-6890. https://doi.org/10.1016/S0040-4039(99)01389-1
- Dreau, M.-A.; Desmaele, D.; Dumas, F.; dAngelo, J. J. Org. Chem.1993, 58, 2933-2935. https://doi.org/10.1021/jo00063a004
- Kim, G.; Kim, J. H.; Lee K. Y. J. Org. Chem. 2006, 7, 2185-2187.
- Lee, H. I.; Cassidy, M. P.; Rashatasakhon, P.; Padwa, A. Org. Lett. 2003, 5, 5067-5070. https://doi.org/10.1021/ol036106r
- Padwa, A.; Lee, H. I.; Rashatasakhon, P.; Rose, M. J. Org. Chem. 2004, 69, 8209-8218. https://doi.org/10.1021/jo048647f
- Shuanhu, G.; Tu, Q. Y.; Hu, X.; Wang, S.; Uua, R.; Jiang, Y.; Zhao, Y.; Fan,X.; Zhang, S. Org. Lett. 2006, 8, 2373-2376. https://doi.org/10.1021/ol0607185
- Tsuda, Y.; Nakai, A.; Ito, K.; Suzuki, F.; Haruna, M. Heterocycles1984, 22, 1817-1820. https://doi.org/10.3987/R-1984-08-1817
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