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(a) Xi, Z.; Goldberg, I. H. Comprehensive Natural Products Chemistry, Eds.; Barton, D. H. R.; Nakanishi, K.; Meth-Cohn, O.; Pergamon: Oxford, 1999; Vol.7, p 553.
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For the structure and reactivities of nine-membered enediynes, see: (a) and references therein
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For the structure and reactivities of nine-membered enediynes, see: (a) Hirama, M.; Akiyama, K.; Das, P.; Mita, T.; Lear, M. J.; Iida, K.; Sato, I.; Yoshimura, F.; Usuki, T.; Tero-Kubota, S. Heterocycles 2006, 69, 83, and references therein.
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(b) Usuki, T.; Mita, T.; Lear, M. J.; Das, P.; Yoshimura, F.; Inoue, M.; Hirama, M.; Akiyama, K.; Tero-Kubota, S. Angew. Chem., Int. Ed. 2004, 43, 5249.
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For synthetic studies of maduropeptin chromophore from our laboratories, see: (a)
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For synthetic studies of maduropeptin chromophore from our laboratories, see: (a) Norizuki, Y.; Komano, K.; Sato, I.; Hirama, M. Chem. Commun. 2008, 5372.
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(c) Komano, K.; Shimamura, S.; Inoue, M.; Hirama, M. J. Am. Chem. Soc. 2007, 129, 14184.
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(d) Kato, N.; Shimamura, S.; Kikai, Y.; Hirama, M. Synlett 2004, 2107.
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(e) Kato, N.; Shimamura, S.; Khan, S.; Takeda, F.; Kikai, Y.; Hirama, M. Tetrahedron 2004, 60, 3161.
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For synthetic studies of maduropeptin chromophore from other laboratories, see: (a)
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For synthetic studies of maduropeptin chromophore from other laboratories, see: (a) Dai, W.-M.; Fong, K. C.; Lau, C. W.; Zhou, L.; Hamaguchi, W.; Nishimoto, S. J. Org. Chem. 1999, 64, 682.
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(d) Nicolaou, K. C.; Koide, K.; Xu, J.; Izraelewicz, M. H. Tetrahedron Lett. 1997, 38, 3671.
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(f) Magnus, P.; Carter, R.; Davies, M.; Elliott, J.; Pitterna, T. Tetrahedron 1996, 52, 6283.
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For the structures of related chromoprotein antibiotics, C-1027, see: (a)
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For the structures of related chromoprotein antibiotics, C-1027, see: (a) Iida, K.; Fukuda, S.; Tanaka, T.; Hirama, M.; Imajo, S.; Ishiguro, M.; Yoshida, K.; Otani, T. Tetrahedron Lett. 1996, 37, 4997.
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Iida, K.1
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Tanaka, T.3
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Otani, T.8
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(b) Iida, K.; Ishii, T.; Hirama, M.; Otani, T.; Minami, Y.; Yoshida, K. Tetrahedron Lett. 1993, 34, 4079.
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(c) Yoshida, K.; Minami, Y.; Azuma, R.; Saeki, M.; Otani, T. Tetrahedron Lett. 1993, 34, 2637.
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25
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Kedarcidin: (d)
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Kedarcidin: (d) Ogawa, K.; Koyama, Y.; Ohashi, I.; Sato, I.; Hirama, M. Angew. Chem., Int. Ed. 2009, 48, 1110.
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(e) Ren, F.; Hogan, P. C.; Anderson, A. J.; Myers, A. G. J. Am. Chem. Soc. 2007, 129, 5381.
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(g) Leet, J. E.; Schroeder, D. R.; Hofstead, S. J.; Golik, J.; Colson, K. L.; Huang, S.; Klohr, S. E.; Doyle, T. W.; Matson, J. A. J. Am. Chem. Soc. 1992, 114, 7946.
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29
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69349088275
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note
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The structure and absolute configuration of 5 was determined by X-ray crystallographic analysis (see Supporting Information).
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31
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0004292616
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Hafner, K.; Lehn, J.-M.; Rees, C. W.; Schleyer, P. von R.; Trost, B. M.; Zahradník, R., Eds.; Springer-Verlag: Berlin
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(b) Oki, M. The Chemistry of Rotational Isomers; Hafner, K.; Lehn, J.-M.; Rees, C. W.; Schleyer, P. von R.; Trost, B. M.; Zahradník, R., Eds.; Springer-Verlag: Berlin, 1993.
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The Chemistry of Rotational Isomers
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(c) Myers, A. G.; Hurd, A. R.; Hogan, P. C. J. Am. Chem. Soc. 2002, 124, 4583.
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Myers, A.G.1
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35
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69349084676
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note
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1b
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36
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35848971002
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For a discussion from a view of the hypothetical biosynthetic pathway, see
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For a discussion from a view of the hypothetical biosynthetic pathway, see: Van Lanen, S. G.; Oh, T.-j.; Liu, W.; Wendt-Pienkowski, E.; Shen, B. J. Am. Chem. Soc. 2007, 129, 13082.
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J. Am. Chem. Soc.
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Van Lanen, S.G.1
Oh, T.-J.2
Liu, W.3
Wendt-Pienkowski, E.4
Shen, B.5
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