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77956691508
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The Sarpagine Group of Indole Alkaloids
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Cordell, G. A., Ed.; Academic Press: San Diego
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Lounasmaa, M.; Hanhinen., P.; Westersund, M. The Sarpagine Group of Indole Alkaloids. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: San Diego, 1999; Vol. 52.
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Lounasmaa, M.1
Hanhinen, P.2
Westersund, M.3
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2
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The synthesis of Macroline Related Alkaloids
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Basha, F. Z., Rahman, A., Eds.; Elsevier Science: Amsterdam
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Bi, Y.; Hamaker, L. K.; Cook, J. M. The Synthesis of Macroline Related Alkaloids. In Studies in Natural Products Chemistry, Bioactive Natural Products, Part A; Basha, F. Z., Rahman, A., Eds.; Elsevier Science: Amsterdam, 1993; Vol. 13, p 383.
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Studies in Natural Products Chemistry, Bioactive Natural Products, Part A
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Bi, Y.1
Hamaker, L.K.2
Cook, J.M.3
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3
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0002452680
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The synthesis of Macroline Related Sarpagine Alkaloids
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Pelletier, S. W., Ed.; Elsevier Science: New York
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Hamaker, L. K.; Cook, J. M. The Synthesis of Macroline Related Sarpagine Alkaloids. In Alkaloids: Chemical and Biological Perspectives; Pelletier, S. W., Ed.; Elsevier Science: New York, 1995; Vol. 9, p 23.
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Hamaker, L.K.1
Cook, J.M.2
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4
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0043040266
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Mukherjee, R.; Melo, M. de F. F.; Santos, Cid A. deM.; Gaittet, E.; Das, B. C. Heterocycles 1990, 31, 1819.
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Mukherjee, R.1
Melo, M.D.F.F.2
Santos, C.A.DeM.3
Gaittet, E.4
Das, B.C.5
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Keawpradub, N.; Eno-Amooquaye, E.; Burke, P. J.; Houghton, P. J. Planta Med. 1999, 65, 311.
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Keawpradub, N.1
Eno-Amooquaye, E.2
Burke, P.J.3
Houghton, P.J.4
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7
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Keawpradub, N.; Kirby, G. C.; Steele, J. C. P.; Houghton, P. J. Planta Med. 1999, 65, 690.
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Keawpradub, N.1
Kirby, G.C.2
Steele, J.C.P.3
Houghton, P.J.4
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8
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37049120789
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Burke, D. E.; DeMarkey, C. A.; LeQuesne, P. W.; Cook, J. M. J. Chem. Soc., Chem. Commun. 1972, 1346.
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Burke, D.E.1
DeMarkey, C.A.2
LeQuesne, P.W.3
Cook, J.M.4
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9
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0028151059
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Bi, Y.; Zhang, L. H.; Hamaker, L. K.; Cook, J. M. J. Am. Chem. Soc. 1994, 116, 9027.
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Bi, Y.1
Zhang, L.H.2
Hamaker, L.K.3
Cook, J.M.4
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12
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0041537406
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note
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The X-ray crystal structure of normacusine B was obtained by Dr.Judy Flippen-Anderson (unpublished results) and confirms the stereo-chemistry as illustrated here.
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13
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0034641496
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a-methyl cases, see: Liu, X.; Wang, T.; Xu, Q.; Ma, C.; Cook, J. M. Tetrahedron Lett. 2000, 41, 6299.
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Liu, X.1
Wang, T.2
Xu, Q.3
Ma, C.4
Cook, J.M.5
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16
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0009268097
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Stotter, P. L.; Friedman, M. D.; Dorsey, G. O.; Shiely, R. W.; Williams, R. F. and Minter, D. E. Heterocycles 1987, 25, 251.
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Stotter, P.L.1
Friedman, M.D.2
Dorsey, G.O.3
Shiely, R.W.4
Williams, R.F.5
Minter, D.E.6
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18
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0041537405
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note
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11B NMR on this compound; however, on the basis of its polarity and analysis of the crude material by NMR spectroscopy, this is the most reasonable structure.
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19
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0031013399
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Cox, E. D.; Hamaker, L. K.; Li, J.; Yu, P.; Czerwinski, K. M.; Deng, L.; Bennett, D. W.; Cook, J. M.; Watson, W. H.; Krawiec, M. J. Org. Chem. 1997, 62, 44.
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J. Org. Chem.
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Cox, E.D.1
Hamaker, L.K.2
Li, J.3
Yu, P.4
Czerwinski, K.M.5
Deng, L.6
Bennett, D.W.7
Cook, J.M.8
Watson, W.H.9
Krawiec, M.10
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21
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0042539471
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Unpublished results
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Other methods to remove the borane from the complex included reagents such as acetic acid. DMAP, etc. (Liu, X.; Cook, J. M. Unpublished results).
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Liu, X.1
Cook, J.M.2
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22
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0034273688
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Many alkaloids in the Strychnos family contain the side chain featured in compounds 11 and 12. For details, see: Bonjoch, J.; Solé, D. Chem. Rev. 2000, 100, 3455.
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Chem. Rev.
, vol.100
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Bonjoch, J.1
Solé, D.2
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