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Volumn 69, Issue 3, 2004, Pages 619-623

Synthesis and Biological Activity of Enantiomers of Antitumor Irofulven

Author keywords

[No Author keywords available]

Indexed keywords

ORGANIC COMPOUNDS; SYNTHESIS (CHEMICAL); TOXICITY;

EID: 0842328956     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo035084j     Document Type: Article
Times cited : (47)

References (17)
  • 8
    • 0842320414 scopus 로고    scopus 로고
    • note
    • Relative configuration was established by analysis of the racemate corresponding to 7, which was obtained in an earlier experiment from the cycloaddition of diazoketone 6 with (±)-5.
  • 9
    • 0842342028 scopus 로고    scopus 로고
    • note
    • Reaction of unprotected 9 with MeMgCl under similar conditions gives the stereoisomeric trans diol in low yield (30%). Cis diol 11 was not detected.
  • 12
    • 0842320409 scopus 로고    scopus 로고
    • note
    • 25D -494.2 (c 2.9 mg/mL, EtOH). This value differs from the value reported in ref 2.
  • 16
    • 0842342023 scopus 로고    scopus 로고
    • Characterization of the Metabolism of the Investigational Anticancer Compound Irofulven and Related Mycotoxins, Illudin S and M, by NADPH-Dependent Alkenal/one Oxidoreductase from the Rat Liver
    • Abstract 2712
    • Dick, R. A.; Yu, X.; Kensler, T. Characterization of the Metabolism of the Investigational Anticancer Compound Irofulven and Related Mycotoxins, Illudin S and M, by NADPH-Dependent Alkenal/one Oxidoreductase from the Rat Liver; Proceedings of American Association of Cancer Research, Annual Meeting, Vol. 44, 1st ed., 2003; Abstract 2712.
    • (2003) Proceedings of American Association of Cancer Research, Annual Meeting, Vol. 44, 1st Ed. , vol.44
    • Dick, R.A.1    Yu, X.2    Kensler, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.