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Volumn 43, Issue 40, 2004, Pages 5342-5346

A β-carboline-1-one mimic of the anticancer Amaryllidaceae constituent pancratistatin: Synthesis and biological evaluation

Author keywords

Antitumor agents; Asymmetric synthesis; Natural products; Pancratistatin; Synthetic methods

Indexed keywords

CELLS; SYNTHESIS (CHEMICAL); TUMORS;

EID: 7244260408     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200460218     Document Type: Article
Times cited : (79)

References (52)
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    • note
    • The pancratistatin, narciclasine, and lycoricidine group of natural products has been collectively referred to as "Amaryllidaceae alkaloids" by most, if not all, synthetic chemists (Martin, Hudlicky, Keck, Poll, and others). Such nomenclature is not accurate as these compounds do not contain basic nitrogen atoms. Another term used in the literature is "isocarbostyril" (Pettit), a term which is correct but not generally known in the synthetic community. To avoid further inaccuracies we will avoid both names in future publications and simply refer to these compounds as "constituents".
  • 2
    • 77957033352 scopus 로고
    • (Ed.: A. R. Brossi), Academic Press, New York
    • For reviews, see: a) S. F. Martin in The Alkaloids, Vol. 40 (Ed.: A. R. Brossi), Academic Press, New York, 1987, pp. 251-376;
    • (1987) The Alkaloids , vol.40 , pp. 251-376
    • Martin, S.F.1
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    • 77956708370 scopus 로고    scopus 로고
    • (Ed.: G. A. Cordell), Academic Press, New York
    • c) O. Hoshino in The Alkaloids, Vol. 51 (Ed.: G. A. Cordell), Academic Press, New York, 1998, pp. 323-424;
    • (1998) The Alkaloids , vol.51 , pp. 323-424
    • Hoshino, O.1
  • 18
    • 0001221503 scopus 로고    scopus 로고
    • for total syntheses of narciclasine, see: q) J. H. Rigby, M. E. Mateo, J. Am. Chem. Soc. 1997, 119, 12655-12656;
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 12655-12656
    • Rigby, J.H.1    Mateo, M.E.2
  • 23
    • 0014199791 scopus 로고
    • b) G. Ceriotti, Nature 1967, 213, 595-596;
    • (1967) Nature , vol.213 , pp. 595-596
    • Ceriotti, G.1
  • 36
    • 0142245701 scopus 로고    scopus 로고
    • A. N. Phung, M. T. Zannetti, G. Whited, W. D. Fessner, Angew. Chem. 2003, 115, 4970-4972; Angew. Chem. Int. Ed. 2003, 42, 4821-4824.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4821-4824
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    • 7244248644 scopus 로고    scopus 로고
    • Accelrys, Inc.
    • a) CHARMm, Accelrys, Inc., 2001;
    • (2001) CHARMm


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.