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Volumn 66, Issue 25, 2010, Pages 4452-4461

Synthesis of 4-haloserotonin derivatives and synthesis of the toad alkaloid dehydrobufotenine

Author keywords

4 Haloserotonins; Coumarins; Dehydrobufotenine; Haloindoles

Indexed keywords

4 BROMOSEROTONIN; 4 CHLOROSEROTONIN; 4 HALOSEROTONIN; ALKALOID; ALLYL COMPOUND; BUFOTENINE; DEHYDROBUFOTENINE; SEROTONIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77953123551     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.04.081     Document Type: Article
Times cited : (14)

References (37)
  • 4
    • 77953122555 scopus 로고    scopus 로고
    • cf
    • cf.
  • 8
    • 77953121124 scopus 로고    scopus 로고
    • cf
    • cf.
  • 9
    • 77953120630 scopus 로고    scopus 로고
    • U.S. Patent 6,022,980
    • Flaugh, M. E. U.S. Patent 6,022,980, 2000.
    • (2000)
    • Flaugh, M.E.1
  • 13
    • 0028600660 scopus 로고
    • For an example based on a zirconocene-stabilized benzyne, see:
    • For an example based on a zirconocene-stabilized benzyne, see:. Tidwell J.H., and Buchwald S.L. J. Am. Chem. Soc. 116 (1994) 11797-11810
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 11797-11810
    • Tidwell, J.H.1    Buchwald, S.L.2
  • 21
    • 37049068465 scopus 로고
    • For one of the few references to the preparation of 4-iodo-5-oxyindoles, see:
    • For one of the few references to the preparation of 4-iodo-5-oxyindoles, see:. Moody C.J., and Swann E. J. Chem. Soc., Perkin Trans. 1 (1993) 2561-2565
    • (1993) J. Chem. Soc., Perkin Trans. 1 , pp. 2561-2565
    • Moody, C.J.1    Swann, E.2
  • 23
    • 77953119578 scopus 로고    scopus 로고
    • cf
    • cf.
  • 26
    • 77953121610 scopus 로고    scopus 로고
    • 2H.
    • 2H.
  • 27
    • 77953123602 scopus 로고    scopus 로고
    • We did not establish if the role of the acid is simply to protonate the nitrogen
    • We did not establish if the role of the acid is simply to protonate the nitrogen.
  • 28
    • 44949129833 scopus 로고    scopus 로고
    • 2 oxidations: Liang, H.; Ciufolini, M.A. J. Org. Chem. 2008, 73, 4299-4301.
    • 2 oxidations: Liang, H.; Ciufolini, M.A. J. Org. Chem. 2008, 73, 4299-4301.
  • 35
    • 77953121267 scopus 로고    scopus 로고
    • We isolated the alkaloid as its iodide; normally it is isolated from natural sources as the chloride
    • We isolated the alkaloid as its iodide; normally it is isolated from natural sources as the chloride.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.