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Part 1; N. Saito, H. Sakai, K. Suwanborirux, S. Pummangura, and A. Kubo, Heterocycles, 2001, 55, 21.
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Heterocycles
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Saito, N.1
Sakai, H.2
Suwanborirux, K.3
Pummangura, S.4
Kubo, A.5
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2
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85087577704
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K. Suwanborirux, S. Amnuoypol, A. Plubrukarn, S. Pummangura, A. Kubo, C. Tanaka, N. Saito unpublished results. see: Okinawa, Nov.
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nd Symposium on The Chemistry of Natural Products (Japan), Okinawa, Nov. 2000, pp. 679-684.
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nd Symposium on The Chemistry of Natural Products (Japan)
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Saito, N.1
Sakai, H.2
Seki, R.3
Kubo, A.4
Suwanborirux, K.5
Pummangura, S.6
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3
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H. He and D. J. Faulkner, J. Org. Chem., 1989, 54, 5822; J. M. Frincke and D. J. Faulkner, J. Am. Chem. Soc., 1982, 104, 265.
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6
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0012007238
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note
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For simplicity, IUPAC numbering of renieramycins is used in this paper, except in the EXPERIMENTAL.
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7
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Kubo, A.4
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b) A. Kubo, N. Saito, H. Yamato, R. Yamauchi, K. Hiruma, and S. Inoue, Chem. Pharm. Bull., 1988, 36, 2607;
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Kurihara, H.1
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b) H. Saito, S. Kobayashi, Y. Uosaki, A. Sato, K. Fujimoto, K. Miyoshi, T. Ashizawa, M. Morimoto, and T. Hirata, Chem. Pharm. Bull., 1990, 38, 1278.
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c) P. Garner, W. B. Ho, and H. Shin, J. Am. Chem. Soc., 1993, 115, 10742.
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d) E. J. Corey, D. Y. Gin, and R. S. Kania, J. Am. Chem. Soc., 1996, 118, 9202.
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e) A. Endo, A. Yanagisawa, M. Abe, S. Tohma, T. Kan, and T. Fukuyama, J. Am. Chem. Soc., 2002, 124, 6552.
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18
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0036300526
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f) K. Suwanborirux, K. Charupant, S. Amnuoypol, S. Pummangura, A. Kubo, and N. Saito, J. Nat. Prod., 2002, 65, 935. Silver tetrafluoroborate has also been used for this type of conversion: see P. Magnus, L. Gazzard, L. Hobson, A. H. Payne, T. J. Rainey, N. Westlund, and V. Lyuch, Tetrahedron, 2002, 58, 3423.
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Kubo, A.5
Saito, N.6
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19
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0037156634
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f) K. Suwanborirux, K. Charupant, S. Amnuoypol, S. Pummangura, A. Kubo, and N. Saito, J. Nat. Prod., 2002, 65, 935. Silver tetrafluoroborate has also been used for this type of conversion: see P. Magnus, L. Gazzard, L. Hobson, A. H. Payne, T. J. Rainey, N. Westlund, and V. Lyuch, Tetrahedron, 2002, 58, 3423.
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Tetrahedron
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Payne, A.H.4
Rainey, T.J.5
Westlund, N.6
Lyuch, V.7
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20
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0011969119
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note
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Cyclic aminal (5b) was easily converted into lactam (2b) using the basic workup in 80-90% yield (see EXPERIMENTAL).
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21
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0025148521
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a) N. Saito, Y. Ohira, and A. Kubo, Chem. Pharm. Bull., 1990, 38, 821.
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b) N. Saito, Y. Ohira, N. Wada, and A. Kubo, Tetrahedron, 1990, 46, 7711.
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23
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SIR97
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Spagna, R.9
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Technical Report of the Crystallography Laboratory University of Nijmegen The Netherlands
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The Kynoch Press, Birmingham, England, Table 1974, 2.2A
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ed. by A. J. C. Wilson, Kluwer Academic Publishers, Boston, Table 4.2.6.8
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e) D. C. Creagh and W. J. McAuley, in International Tables for Crystallography, Vol. C, ed. by A. J. C. Wilson, Kluwer Academic Publishers, Boston, Table 4.2.6.8, 1992, pp. 219-222.
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