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Volumn 50, Issue C, 1998, Pages 109-139

Chapter 3 Biological Activity of Unnatural Alkaloid Enantiomers

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EID: 33847577096     PISSN: 10994831     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1099-4831(08)60041-3     Document Type: Article
Times cited : (11)

References (116)
  • 10
    • 77956668369 scopus 로고
    • Jefford C.W., Reinhart K.L., and Shield L.S. (Eds), Technomic Publishing Co., Basel
    • Brossi A., and Schönenberger B. In: Jefford C.W., Reinhart K.L., and Shield L.S. (Eds). Pharmaceuticals and the Sea (1988), Technomic Publishing Co., Basel 135
    • (1988) Pharmaceuticals and the Sea , pp. 135
    • Brossi, A.1    Schönenberger, B.2
  • 48
    • 0001778685 scopus 로고
    • Phillipson J.D., Roberts M.F., and Zenk M.H. (Eds), Springer-Verlag, New York
    • Rice K.C. In: Phillipson J.D., Roberts M.F., and Zenk M.H. (Eds). The Chemistry and Biology of Isoquinoline Alkaloids (1985), Springer-Verlag, New York 191-203
    • (1985) The Chemistry and Biology of Isoquinoline Alkaloids , pp. 191-203
    • Rice, K.C.1
  • 64
    • 0003799361 scopus 로고
    • Burger A. (Ed), Wiley-Interscience, New York
    • Gearien J.E. In: Burger A. (Ed). Medicinal Chemistry (1970), Wiley-Interscience, New York 1310
    • (1970) Medicinal Chemistry , pp. 1310
    • Gearien, J.E.1
  • 88
    • 0020169638 scopus 로고
    • The aS absolute configuration of the phenyl-tropolone system in natural (-)-colchicine follows the chirality rules which consider the order of the ortho-ortho substitutents of the central bond. M. F. Mackay, Department of Chemistry, La Trobe University, Bundoora, Victoria 3083, Australia, informs us that natural (-)-colchicine according to rules established in 1966 by Cahn, Ingold, and Prelog would have aR absolute configuration of the phenyl-tropolone system. In assigning the absolute axial configuration to colchicinoids it is important therefore, to explain on what ruling it is based
    • Prelog V., and Helmchen G. Angew, Chem. Int. Ed. Engl. 21 (1982) 567 The aS absolute configuration of the phenyl-tropolone system in natural (-)-colchicine follows the chirality rules which consider the order of the ortho-ortho substitutents of the central bond. M. F. Mackay, Department of Chemistry, La Trobe University, Bundoora, Victoria 3083, Australia, informs us that natural (-)-colchicine according to rules established in 1966 by Cahn, Ingold, and Prelog would have aR absolute configuration of the phenyl-tropolone system. In assigning the absolute axial configuration to colchicinoids it is important therefore, to explain on what ruling it is based
    • (1982) Angew, Chem. Int. Ed. Engl. , vol.21 , pp. 567
    • Prelog, V.1    Helmchen, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.