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1
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0141847135
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Cordell, G. A., Ed., in press.
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For reviews of the Lycopodium alkaloids, see: (a) Kobayashi, J.; Morita, H. The Alkaloids; Cordell, G. A., Ed., in press.
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The Alkaloids
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Kobayashi, J.1
Morita, H.2
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2
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77957098031
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(b). G.A. Cordell, & A. Brossi. New York: Academic
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(b) Ayer W.A., Trifonov L.S. Cordell G.A., Brossi A. The Alkaloids. Vol. 45:1994;233 Academic, New York
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Ayer, W.A.1
Trifonov, L.S.2
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4
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77957072064
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Brossi A. New York: Academic
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MacLean D.B. Brossi A. The Alkaloids. Vol. 26:1985;241 Academic, New York
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The Alkaloids
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MacLean, D.B.1
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5
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0000762599
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Manske R.H.F. New York: Academic
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MacLean D.B. Manske R.H.F. The Alkaloids. Vol. 14:1973;348 Academic, New York
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The Alkaloids
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MacLean, D.B.1
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6
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25144521742
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Manske R.H.F. New York: Academic
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MacLean D.B. Manske R.H.F. The Alkaloids. Vol. 10:1968;305 Academic, New York
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The Alkaloids
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MacLean, D.B.1
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9
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84922342912
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Liu J.S., Zhu Y.L., Yu C.M., Zhou Y.Z., Han Y.Y., Wu F.W., Qi B.F. Can J. Chem. 64:1986;837-839
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Can J. Chem.
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Liu, J.S.1
Zhu, Y.L.2
Yu, C.M.3
Zhou, Y.Z.4
Han, Y.Y.5
Wu, F.W.6
Qi, B.F.7
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13
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0028030656
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Williams J.P., St. Laurent D.R., Friedrich D., Pinard E., Roden B.A., Paquette L.A. J. Am. Chem. Soc. 116:1994;4689-4696
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Williams, J.P.1
St. Laurent, D.R.2
Friedrich, D.3
Pinard, E.4
Roden, B.A.5
Paquette, L.A.6
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23
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0344785207
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Braekman C., Nyembo L., Bourdoux P., Kahindo N., Hootele C. Phytochemistry. 13:1974;2519-2528
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Phytochemistry
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Braekman, C.1
Nyembo, L.2
Bourdoux, P.3
Kahindo, N.4
Hootele, C.5
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26
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0033534623
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Tori M., Shimoji T., Takaoka S., Nakashima K., Sono M., Ayer W.A. Tetrahedron Lett. 40:1999;323-324
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Tori, M.1
Shimoji, T.2
Takaoka, S.3
Nakashima, K.4
Sono, M.5
Ayer, W.A.6
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27
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3242695268
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Tori M., Shimoji T., Shimura E., Takaoka S., Nakashima K., Sono M., Ayer W.A. Phytochemistry. 503:2000;509
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Phytochemistry
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Tori, M.1
Shimoji, T.2
Shimura, E.3
Takaoka, S.4
Nakashima, K.5
Sono, M.6
Ayer, W.A.7
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30
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84986437005
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Conformational search and molecular mechanics calculations were conducted by Macromodel program and energetically stable conformer was shown in Figure 4:
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Conformational search and molecular mechanics calculations were conducted by Macromodel program and energetically stable conformer was shown in Figure 4: 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. 11:1990;440-467
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(1990)
J. Comput. Chem.
, vol.11
, pp. 440-467
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Mohamadi, F.1
Richards, N.G.J.2
Guida, W.C.3
Liskamp, R.4
Lipton, M.5
Caufield, C.6
Chang, G.7
Hendrickson, T.8
Still, W.C.9
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32
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3242724213
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note
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13C NMR assignments of cernuine (9) and lycocernuine (10) were conducted by 2D NMR analysis, since there were no reports on their assignments
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-
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36
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3242686211
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50 value of 1.6 μM
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50 value of 1.6 μM
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-
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37
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3242739392
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D values of 1-3 were not reliable due to small amount of samples and small values of optical rotations
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