참고문헌
- Paquette, L. A.; Mendez-Andino, J. Tetrahedron Lett. 1999, 40, 4301 https://doi.org/10.1016/S0040-4039(99)00781-9
- Choudhury, P. K.; Foubelo, F.; Yus, M. Tetrahedron Lett. 1998, 39, 3581 https://doi.org/10.1016/S0040-4039(98)00554-1
- Loh, T.-P.; Lye, P.-L. Tetrahedron Lett. 2001, 42, 3511 https://doi.org/10.1016/S0040-4039(01)00492-0
- Lee, K.-H.; Ibuka, T.; Kim, S.-H.; Vestal, B. R.; Hall, I. H. J. Med. Chem. 1975, 18, 812 https://doi.org/10.1021/jm00242a010
- Kabalka, G. W.; Venkataiah, B.; Chen, C. Tetrahedron Lett. 2006, 47, 4187 https://doi.org/10.1016/j.tetlet.2006.04.063
- Sidduri, A.-R.; Knochel, P. J. Am. Chem. Soc. 1992, 114, 7579 https://doi.org/10.1021/ja00045a050
- Sidduri, A.-R.; Rozema, M. J.; Knochel, P. J. Org. Chem. 1993, 58, 2694 https://doi.org/10.1021/jo00062a010
- Peng, H.; Kim, D.-I.; Sarkaria, J. N.; Cho, Y.-S.; Abraham, R. T.; Zalkow, L. H. Bioorg. Med. Chem. 2002, 10, 167 https://doi.org/10.1016/S0968-0896(01)00260-7
- Nozaki, K.; Oshima, K.; Utimoto, K. Bull. Chem. Soc. Jpn. 1987, 60, 3465 https://doi.org/10.1246/bcsj.60.3465
- Kennedy, J. W. J.; Hall, D. G. J. Am. Chem. Soc. 2002, 124, 898 https://doi.org/10.1021/ja016391e
- Kennedy, J. W. J.; Hall, D. G. J. Am. Chem. Soc. 2002, 124, 11586 https://doi.org/10.1021/ja027453j
- Kennedy, J. W. J.; Hall, D. G. J. Org. Chem. 2004, 69, 4412 https://doi.org/10.1021/jo049773m
- Ghatak, A.; Sarkar, S.; Ghosh, S. Tetrahedron 1997, 53, 17335 https://doi.org/10.1016/S0040-4020(97)10157-0
- Sarkar, S.; Ghosh, S. Tetrahedron Lett. 1996, 37, 4809 https://doi.org/10.1016/0040-4039(96)00942-2
- Mandal, P. K.; Maiti, G.; Roy, S. C. J. Org. Chem. 1998, 63, 2829 https://doi.org/10.1021/jo971526d
- Saicic, R. N.; Zard, S. Z. Chem. Commun. 1996, 1631
- Maiti, G.; Roy, S. C. J. Chem. Soc., Perkin Trans. 1 1996, 403
- Hon, Y.-S.; Hsieh, C.-H.; Liu, Y.-W. Tetrahedron 2005, 61, 2713 https://doi.org/10.1016/j.tet.2005.01.057
- Bella, M.; Margarita, R.; Orlando, C.; Orsini, M.; Parlanti, L.; Piancatelli, G. Tetrahedron Lett. 2000, 41, 561 https://doi.org/10.1016/S0040-4039(99)02119-X
- Drioli, S.; Felluga, F.; Forzato, C.; Nitti, P.; Pitacco, G.; Valentin, E. J. Org. Chem. 1998, 63, 2385 https://doi.org/10.1021/jo972032j
- Pohmakotr, M.; Harnying, W.; Tuchinda, P.; Reutrakul, V. Helv. Chim. Acta 2002, 85, 3792 https://doi.org/10.1002/1522-2675(200211)85:11<3792::AID-HLCA3792>3.0.CO;2-Q
- Biel, M.; Kretsovali, A.; Karatzali, E.; Papamatheakis, J.; Giannis, A. Angew. Chem. Int. Ed. 2004, 43, 3974 https://doi.org/10.1002/anie.200453879
- Srikrishna, A. J. Chem. Soc., Chem. Commun. 1987, 587
- Isaac, M. B.; Paquette, L. A. J. Org. Chem. 1997, 62, 5333 https://doi.org/10.1021/jo970267p
- Paquette, L. A.; Bennett, G. D.; Chhatriwalla, A.; Isaac, M. B. J. Org. Chem. 1997, 62, 3370 https://doi.org/10.1021/jo970158a
- Paquette, L. A.; Bennett, G. D.; Isaac, M. B.; Chhatriwalla, A. J. Org. Chem. 1998, 63, 1836 https://doi.org/10.1021/jo9715534
- Paquette, L. A.; Rothhaar, R. R.; Isaac, M.; Rogers, L. M.; Rogers, R. D. J. Org. Chem. 1998, 63, 5463 https://doi.org/10.1021/jo980372e
- Choudhury, P. K.; Foubelo, F.; Yus, M. J. Org. Chem. 1999, 64, 3376 https://doi.org/10.1021/jo982311m
- Kang, S.-K.; Baik, T.-G.; Jiao, X.-H. Synth. Commun. 2002, 32, 75 https://doi.org/10.1081/SCC-120001511
- Reddy, G. V.; Rao, G. V.; Iyengar, D. S. Tetrahedron Lett. 1999, 40, 3937 https://doi.org/10.1016/S0040-4039(99)00614-0
- Kamal, A.; Reddy, G. S. K.; Reddy, K. L. Tetrahedron Lett. 2001, 42, 6969. 8
- Lee, M. J.; Kim, S. C.; Kim, J. N. Bull. Korean Chem. Soc. 2006, 27, 140 https://doi.org/10.5012/bkcs.2006.27.1.140
- Lee, K. Y.; Kim, S. C.; Kim, J. N. Bull. Korean Chem. Soc. 2006, 27, 319 https://doi.org/10.5012/bkcs.2006.27.2.319
- Lee, K. Y.; Kim, S. C.; Kim, J. N. Tetrahedron Lett. 2006, 47, 977 https://doi.org/10.1016/j.tetlet.2005.11.142
- Lee, K. Y.; Seo, J.; Kim, J. N. Tetrahedron Lett. 2006, 47, 3913 https://doi.org/10.1016/j.tetlet.2006.03.167
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