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Volumn 49, Issue 32, 2008, Pages 4780-4783

The synthesis of compounds related to the indole-indoline core of the vinca alkaloids (+)-vinblastine and (+)-vincristine

Author keywords

Alkaloid; Analogs; Arylation; Indole; Indoline; Vinblastine; Vincristine

Indexed keywords

VINBLASTINE; VINCA ALKALOID; VINCRISTINE;

EID: 45649083379     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.05.082     Document Type: Article
Times cited : (19)

References (38)
  • 1
    • 45649084839 scopus 로고    scopus 로고
    • 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.
  • 9
    • 4344629173 scopus 로고    scopus 로고
    • 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
  • 26
    • 4344622281 scopus 로고    scopus 로고
    • 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
  • 34
    • 0001577916 scopus 로고
    • 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
    • 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
    • 45649085480 scopus 로고    scopus 로고
    • note
    • +{radical dot}, 474.2155.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.