참고문헌
- Arai, K.; Yamamoto, Y. Chem. Pharm. Bull. 1990, 38, 2929 https://doi.org/10.1248/cpb.38.2929
- Kaji, A.; Saito, R.; Nomura, M.; Miyamoto, K.; Kiriyama, N. Biol. Pharm. Bull. 1998, 21, 945 https://doi.org/10.1248/bpb.21.945
- Brewer, D.; Jerram, W.; Taylor, A. Can. J. Microbiol. 1968, 14, 861 https://doi.org/10.1139/m68-145
- Sekita, S. Chem. Pharm. Bull. 1983, 31, 2998 https://doi.org/10.1248/cpb.31.2998
- Kaji, A.; Saito, R.; Hata, Y.; Kiriyama, N. Chem. Pharm. Bull. 1999, 47, 77 https://doi.org/10.1248/cpb.47.77
- Arai, K.; Shimizu, S.; Taguchi, Y.; Yamamoto, Y. Chem. Pharm. Bull. 1981, 29, 991 https://doi.org/10.1248/cpb.29.991
- Shimizu, S.; Yamamoto, Y.; Koshimura, S. Chem. Pharm. Bull. 1982, 30, 1896 https://doi.org/10.1248/cpb.30.1896
- Kaji, A.; Iwata, T.; Kiriyama, N.; Wakusawa, S.; Miyamoto, K. Chem. Pharm. Bull. 1994, 42, 1682 https://doi.org/10.1248/cpb.42.1682
- Alvi, K. A.; Pu, H.; Luche, M.; Rice, A.; App, H.; McMahon, G.; Dare, H.; Margolis, B. J. Antibiot. 1999, 52, 215 https://doi.org/10.7164/antibiotics.52.215
- Kaji, A.; Saito, R.; Nomura, M.; Miyamoto, K.; Kiriyama, N. Anticancer Res. 1997, 17, 3675
- Zhang, B.; Salituro, G.; Szalkowski, D.; Li, Z.; Zhang, Y.; Royo, I.; Vilella, D.; Diez, M. T.; Pelaez, F.; Ruby, C.; Kendall, R. L.; Mao, X.; Griffin, P.; Calaycay, J.; Zierath, J. R.; Heck, J. V.; Smith, R. G.; Moller, D. E. Science 1999, 284, 974 https://doi.org/10.1126/science.284.5416.974
- Mohlau, R.; Redlich, R. Ber. Dtsch. Chem. Ges. 1911, 44, 3605 https://doi.org/10.1002/cber.191104403245
- Bu'Lock, J. D.; Harley-Mason, J. J. Chem. Soc. 1951, 703 https://doi.org/10.1039/jr9510000703
- Maiti, A. K.; Bhattacharya, P. J. Chem. Res. (S) 1997, 424
- Yadav, J. S.; Reddy, B. V. S.; Swamy, T. Tetrahedron Lett. 2003, 44, 9121 https://doi.org/10.1016/j.tetlet.2003.10.041
- Yadav, J. S.; Reddy, B. V. S.; Swamy, T. Synthesis 2004, 1, 106
- Pirrung, M. C.; Park, K.; Li, Z. Org. Lett. 2001, 3, 365 https://doi.org/10.1021/ol006852l
- Pirrung, M. C.; Deng, L.; Li, Z.; Park, K. J. Org. Chem. 2002, 67, 8374 https://doi.org/10.1021/jo0204597
- Kappe, C. O. Angew. Chem. Int. Ed. 2004, 43, 6250 https://doi.org/10.1002/anie.200400655
- Wathey, B.; Tiemey, J.; Lidstrom, P.; Westman, J. Drug Discovery Today 2002, 7, 373 https://doi.org/10.1016/S1359-6446(02)02178-5
- Lidstrom, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225 https://doi.org/10.1016/S0040-4020(01)00906-1
- Lew, A.; Krutzik, P. O.; Hart, M. E.; Chamberlin, A. R. J. Comb. Chem. 2002, 4, 95 https://doi.org/10.1021/cc010048o
- Perreux, L.; Loupy, A. Tetrahedron 2001, 57, 9199 https://doi.org/10.1016/S0040-4020(01)00905-X
- Lidstrom, P.; Tierney, J.; Wathey, B.; Westman, J. Tetrahedron 2001, 57, 9225 https://doi.org/10.1016/S0040-4020(01)00906-1
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