-
1
-
-
45649084839
-
-
Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). In The Alkaloids, Brossi, A., Suffness, M., Eds.; Academic Press: New York, 1990; Vol. 37, pp 1-240 and references cited therein.
-
Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). In The Alkaloids, Brossi, A., Suffness, M., Eds.; Academic Press: New York, 1990; Vol. 37, pp 1-240 and references cited therein.
-
-
-
-
2
-
-
36348942481
-
-
See, for example:
-
See, for example:. Miyazaki T., Yokoshima S., Simizu S., Osada H., Tokuyama H., and Fukuyama T. Org. Lett. 9 (2007) 4737
-
(2007)
Org. Lett.
, vol.9
, pp. 4737
-
-
Miyazaki, T.1
Yokoshima, S.2
Simizu, S.3
Osada, H.4
Tokuyama, H.5
Fukuyama, T.6
-
3
-
-
34249939199
-
-
Shao Y., Ding H., Tang W., Lou L., and Hu L. Bioorg. Med. Chem. 15 (2007) 5061
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 5061
-
-
Shao, Y.1
Ding, H.2
Tang, W.3
Lou, L.4
Hu, L.5
-
4
-
-
34548228429
-
-
Li W., Shao Y., Hu L., Zhang X., Chen Y., Tong L., Li C., Shen X., and Ding J. Cancer Biol. Ther. 6 (2007) 787
-
(2007)
Cancer Biol. Ther.
, vol.6
, pp. 787
-
-
Li, W.1
Shao, Y.2
Hu, L.3
Zhang, X.4
Chen, Y.5
Tong, L.6
Li, C.7
Shen, X.8
Ding, J.9
-
8
-
-
19544393159
-
-
Gigant B., Wang C., Ravelli R.B.G., Roussi F., Steinmetz M.O., Curmi P.A., Sobel A., and Knossow M. Nature 435 (2005) 519
-
(2005)
Nature
, vol.435
, pp. 519
-
-
Gigant, B.1
Wang, C.2
Ravelli, R.B.G.3
Roussi, F.4
Steinmetz, M.O.5
Curmi, P.A.6
Sobel, A.7
Knossow, M.8
-
9
-
-
4344629173
-
-
For useful points-of-entry into the literature on studies directed towards the total synthesis of the title alkaloids see:
-
For useful points-of-entry into the literature on studies directed towards the total synthesis of the title alkaloids see:. Kuboyama T., Yokoshima S., Tokuyama H., and Fukuyama T. Proc. Natl. Acad. Sci. U.S.A. 101 (2004) 11966
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 11966
-
-
Kuboyama, T.1
Yokoshima, S.2
Tokuyama, H.3
Fukuyama, T.4
-
10
-
-
0037070544
-
-
Yokoshima S., Ueda T., Kobayashi S., Sato A., Kuboyama T., Tokuyama H., and Fukuyama T. J. Am. Chem. Soc. 124 (2002) 2137
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 2137
-
-
Yokoshima, S.1
Ueda, T.2
Kobayashi, S.3
Sato, A.4
Kuboyama, T.5
Tokuyama, H.6
Fukuyama, T.7
-
11
-
-
0027077957
-
-
Magnus P., Mendoza J.S., Stamford A., Ladlow M., and Willis P. J. Am. Chem. Soc. 114 (1992) 10232
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 10232
-
-
Magnus, P.1
Mendoza, J.S.2
Stamford, A.3
Ladlow, M.4
Willis, P.5
-
13
-
-
0000352444
-
-
Kutney J.P., Choi L.S.L., Nakano J., Tsukamoto H., McHugh M., and Boulet C.A. Heterocycles 27 (1988) 1845
-
(1988)
Heterocycles
, vol.27
, pp. 1845
-
-
Kutney, J.P.1
Choi, L.S.L.2
Nakano, J.3
Tsukamoto, H.4
McHugh, M.5
Boulet, C.A.6
-
14
-
-
0018388614
-
-
Mangeney P., Andriamialisoa R.Z., Langlois N., Langlois Y., and Potier P. J. Am. Chem. Soc. 101 (1979) 2243
-
(1979)
J. Am. Chem. Soc.
, vol.101
, pp. 2243
-
-
Mangeney, P.1
Andriamialisoa, R.Z.2
Langlois, N.3
Langlois, Y.4
Potier, P.5
-
16
-
-
33747600674
-
-
Ishikawa H., Elliot G.I., Velcicky J., Choi Y., and Boger D.L. J. Am. Chem. Soc. 128 (2006) 10596
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 10596
-
-
Ishikawa, H.1
Elliot, G.I.2
Velcicky, J.3
Choi, Y.4
Boger, D.L.5
-
20
-
-
34250170875
-
-
See, for example:
-
See, for example:. Hu L., Jiang J.-d., Qu J., Li Y., Jin J., Li Z.-r., and Boykin D.W. Bioorg. Med. Chem. Lett. 17 (2007) 3613
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 3613
-
-
Hu, L.1
Jiang, J.-d.2
Qu, J.3
Li, Y.4
Jin, J.5
Li, Z.-r.6
Boykin, D.W.7
-
21
-
-
34249323026
-
-
Álvarez C., Álvarez R., Corchete P., Pérez-Melero C., Peláez R., and Medarde M. Bioorg. Med. Chem. Lett. 17 (2007) 3417
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 3417
-
-
Álvarez, C.1
Álvarez, R.2
Corchete, P.3
Pérez-Melero, C.4
Peláez, R.5
Medarde, M.6
-
22
-
-
23644443814
-
-
Romagnoli R., Baraldi P.G., Jung M.K., Iaconinoto M.A., Carrion M.D., Remusat V., Preti D., Tabrizi M.A., Francesca F., De Clercq E., Balzarini J., and Hamel E. Bioorg. Med. Chem. Lett. 15 (2005) 4048
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 4048
-
-
Romagnoli, R.1
Baraldi, P.G.2
Jung, M.K.3
Iaconinoto, M.A.4
Carrion, M.D.5
Remusat, V.6
Preti, D.7
Tabrizi, M.A.8
Francesca, F.9
De Clercq, E.10
Balzarini, J.11
Hamel, E.12
-
23
-
-
0032492959
-
-
Pettit G.R., Toki B., Herald D.L., Verdier-Pinard P., Boyd M.R., Hamel E., and Pettit R.K. J. Med. Chem. 41 (1998) 1688
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1688
-
-
Pettit, G.R.1
Toki, B.2
Herald, D.L.3
Verdier-Pinard, P.4
Boyd, M.R.5
Hamel, E.6
Pettit, R.K.7
-
24
-
-
0026582270
-
-
Getahun Z., Jurd L., Chu P.S., Lin C.M., and Hamel E. J. Med. Chem. 35 (1992) 1058
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1058
-
-
Getahun, Z.1
Jurd, L.2
Chu, P.S.3
Lin, C.M.4
Hamel, E.5
-
26
-
-
4344622281
-
-
This type of protocol has also been extended to the synthesis of quinolines and related systems:
-
This type of protocol has also been extended to the synthesis of quinolines and related systems:. Banwell M.G., Lupton D.W., Ma X., Renner J., and Sydnes M.O. Org. Lett. 6 (2004) 2741
-
(2004)
Org. Lett.
, vol.6
, pp. 2741
-
-
Banwell, M.G.1
Lupton, D.W.2
Ma, X.3
Renner, J.4
Sydnes, M.O.5
-
32
-
-
0026500938
-
-
Johnson C.R., Adams J.P., Braun M.P., Senanayake C.B.W., Wovkulich P.M., and Uskoković M.R. Tetrahedron Lett. 33 (1992) 917
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 917
-
-
Johnson, C.R.1
Adams, J.P.2
Braun, M.P.3
Senanayake, C.B.W.4
Wovkulich, P.M.5
Uskoković, M.R.6
-
34
-
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0001577916
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This and the other aryl lead compounds reported here, viz. compounds 13a-e, were prepared using protocols defined by Pinhey and co-workers: Details will be provided in a forthcoming full paper
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This and the other aryl lead compounds reported here, viz. compounds 13a-e, were prepared using protocols defined by Pinhey and co-workers:. Kozyrod R.P., Morgan J., and Pinhey J.T. Aust. J. Chem. 38 (1985) 1147 Details will be provided in a forthcoming full paper
-
(1985)
Aust. J. Chem.
, vol.38
, pp. 1147
-
-
Kozyrod, R.P.1
Morgan, J.2
Pinhey, J.T.3
-
37
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45649085480
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note
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+{radical dot}, 474.2155.
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