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Yamamura, S.1
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Brossi, A., Ed.; Academic Press: New York
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For reviews of the Daphniphyllum alkaloids, see: (a) Yamamura, S.; Hirata, Y. In The Alkaloids; Manske, R. H. F., Ed., Academic Press: New York, 1975; Vol. 15, p 41. (b) Yamamura, S. In The Alkaloids; Brossi, A., Ed.; Academic Press: New York, 1986; Vol. 29, p 265.
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0343171370
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In the previous study, yuzurimine as a major alkaloid, and secodaphniphylline, daphniteijsmine, deoxyyuzurimine, and isodaphnilactone-B as minor ones have been isolated from D. humile: Yamamura, S.; Terada, Y. Chem. Lett. 1976, 1381-1382.
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(c) Tempesta, M. S.; Corley, D. G.; Beutler, J. A.; Metral, C. J.; Yunes, R. A.; Giacomozzi, C. A.; Calixto, J. B. J. Nat. Prod. 1988, 51, 617-618.
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25
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84986437005
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Monte Carlo simulation and molecular mechanics calculations were conducted by Macromodel program: Mohamadi, F.; Richards, N. G. J.; Guida, W. C.; Liskamp, R.; Lipton, M.; Caufield, C.; Chang, G.; Hendrickson, T.; Still, W. C. J, Comput. Chem. 1990, 11, 440-467.
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Hendrickson, T.8
Still, W.C.9
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26
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0342736968
-
-
note
-
Broad signals of H-2b, H-3a, H-4, H-19, and H-21 located at or near the 1-azabicyclo[5.2.2]undecane ring at 300 K were changed to fairly sharp ones at 250 K.
-
-
-
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27
-
-
0342736969
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-
note
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H 2.34 and 4.26; this difference may be due to the presence of the carbonyl group at C-7.
-
-
-
-
28
-
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0342301909
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-
note
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H 3.32 and 3.28, respectively) were very close to each other.
-
-
-
-
30
-
-
0342736966
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-
note
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15 for 2a belonging to the major cluster, were consistent with the NOESY data and the proton coupling (6.4 Hz) observed.
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31
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20444483055
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3)-H system in the Macromodel program: Haasnoot, C. A. G.; de Leeuw, F. A. A. M.; Altona, C. Tetrahedron 1980, 36, 2783-2792.
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(1980)
Tetrahedron
, vol.36
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-
Haasnoot, C.A.G.1
De Leeuw, F.A.A.M.2
Altona, C.3
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