참고문헌
- Robinson, D. E. J. E.; Bull, S. D. Tetrahedron: Asymmetry 2003, 14, 1407 https://doi.org/10.1016/S0957-4166(03)00209-X
- Keith, J. M.; Larrow, J. F.; Jacobson, E. N. Adv. Synth. Catal. 2001, 343, 5 https://doi.org/10.1002/1615-4169(20010129)343:1<5::AID-ADSC5>3.0.CO;2-I
- Chen, T.; Jiang, J.-J.; Xu, Q.; Shi, M. Org. Lett. 2007, 9, 865 https://doi.org/10.1021/ol063061w
- Mueller, J. A.; Cowell, A.; Chandler, B. D.; Sigman, M. S. J. Am. Chem. Soc. 2005, 127, 14817 https://doi.org/10.1021/ja053195p
- Trend, R. M.; Stoltz, B. M. J. Am. Chem. Soc. 2004, 126, 4482 https://doi.org/10.1021/ja039551q
- Mazet, C.; Roseblade, S.; Köhler, V.; Pfaltz, A. Org. Lett. 2006, 8, 1879 https://doi.org/10.1021/ol060443t
- Yamada, S.; Misono, T.; Iwai, Y. Tetrahedron Lett. 2005, 46, 2239 https://doi.org/10.1016/j.tetlet.2005.02.019
- Suzuki, Y.; Yamauchi, K.; Muramatsu, K.; Sato, M. Chem. Commun. 2004, 2770
- Kim, Y.; Choi, E. T.; Lee, M. H.; Park, Y. S. Tetrahedron Lett. 2007, 48, 2833 https://doi.org/10.1016/j.tetlet.2007.02.111
- Choi, E. T.; Lee, M. H.; Kim, Y.; Park, Y. S. Tetrahedron 2008, 64, 1515 https://doi.org/10.1016/j.tet.2007.11.026
- Shin, E.-k.; Chang, J.-y.; Kim, H. J.; Kim, Y.; Park, Y. S. Bull. Korean Chem. Soc. 2006, 27, 447 https://doi.org/10.5012/bkcs.2006.27.3.447
- Chang, J.-y.; Shin, E.-k.; Kim, H. J.; Kim, Y.; Park, Y. S. Bull. Korean Chem. Soc. 2005, 26, 989 https://doi.org/10.5012/bkcs.2005.26.6.989
- Chang, J.-y.; Shin, E.-k.; Kim, H. J.; Kim, Y.; Park, Y. S. Tetrahedron 2005, 61, 2743 https://doi.org/10.1016/j.tet.2005.01.091
- Nam, J.; Chang, J.-y.; Shin, E.-k.; Kim, H. J.; Kim, Y.; Jang, S.; Park, Y. S. Tetrahedron 2004, 60, 6311 https://doi.org/10.1016/j.tet.2004.05.094
- Nam, J.; Chang, J.-y.; Hahm, K.-S.; Park, Y. S. Tetrahedron Lett. 2003, 44, 7727 https://doi.org/10.1016/j.tetlet.2003.08.091
- Kang, K. H.; Lee, M. H.; Choi, E. T.; Park, Y. S. Bull. Korean Chem. Soc. 2007, 28, 1199 https://doi.org/10.5012/bkcs.2007.28.7.1199
- Quaglia, W.; Pigini, M.; Piergentili, A.; Ginnella, M.; Gentili, F.; Marucci, G.; Carrieri, A.; Carotti, A.; Poggesi, E.; Leonardi, A.; Melchiorre, C. J. Med. Chem. 2002, 45, 1633 https://doi.org/10.1021/jm011066n
- Bailly, C.; Bal, C.; Barbier, P.; Combes, S.; Finet, J.-P.; Hildebrand, M.-P.; Peyrot, V.; Wattez, N. J. Med. Chem. 2003, 46, 5437 https://doi.org/10.1021/jm030903d
- Hajra, S.; Maji, B.; Karmakar, A. Tetrahedron Lett. 2005, 46, 8599 https://doi.org/10.1016/j.tetlet.2005.09.170
- Barluenga, J.; Trincado, M.; Rubio, E.; Gonzalez, J. M. J. Am. Chem. Soc. 2004, 126, 3416 https://doi.org/10.1021/ja0397299
- Sakai, K.; Fujimoto, M.; Mihara, S.-i.; Yamamori, T. J. Med. Chem. 2002, 45, 2041 https://doi.org/10.1021/jm010382z
- Andres, J. M.; Martin, Y.; Pedrosa, R.; Perez-Encabo, A. Tetrahedron 1997, 53, 3787 https://doi.org/10.1016/S0040-4020(97)00099-9
- Denmark, S. E.; Beutner, G. L.; Wynn, T.; Eastgate, M. D. J. Am. Chem. Soc. 2005, 127, 3774 https://doi.org/10.1021/ja047339w
- Carreira, E. M.; Singer, R. A.; Lee, W. J. Am. Chem. Soc. 1994, 116, 8837 https://doi.org/10.1021/ja00098a065
- Rutherford, A. P.; Gibb, C. G.; Hartley, R. C.; Goodman, J. M. J. Chem. Soc., Perkin Trans. 1 2001, 1051
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