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Volumn 11, Issue 3, 2013, Pages 515-522

Synthesis and cytotoxicity of (+/-)-7,9-dideoxy-pancratistatin analogues

Author keywords

[No Author keywords available]

Indexed keywords

CHEMISTRY; POSITIVE IONS;

EID: 84871094932     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob27127c     Document Type: Article
Times cited : (17)

References (47)
  • 3
    • 47249124531 scopus 로고    scopus 로고
    • See also the "Introduction" section of ref. 15b and references cited therein Pancratistatin was discovered by Pettit in 1984
    • A. Kornienko A. Evidente Chem. Rev. 2008 108 1982 2014
    • (2008) Chem. Rev. , vol.108 , pp. 1982-2014
    • Kornienko, A.1    Evidente, A.2
  • 10
    • 79951527897 scopus 로고    scopus 로고
    • For an account covering the progress in the synthesis of Amaryllidaceae constituents and some truncated derivatives from 1996 to the fall of 2004, with a detailed treatment of the total synthesis of pancratistatin, narciclasine, 7-deoxypancratistatin and lycoricidine, see
    • J. McNulty A. Thorat N. Vurgun J. J. Nair E. Makaji D. J. Crankshaw A. C. Holloway S. Pandey J. Nat. Prod. 2011 74 106 108
    • (2011) J. Nat. Prod. , vol.74 , pp. 106-108
    • McNulty, J.1    Thorat, A.2    Vurgun, N.3    Nair, J.J.4    Makaji, E.5    Crankshaw, D.J.6    Holloway, A.C.7    Pandey, S.8
  • 11
    • 14644422595 scopus 로고    scopus 로고
    • For a review on the total synthesis of pancratistatin, see
    • U. Rinner T. Hudlicky Synlett 2005 365 387
    • (2005) Synlett , pp. 365-387
    • Rinner, U.1    Hudlicky, T.2
  • 14
    • 80055084410 scopus 로고    scopus 로고
    • For a most recent compilation of research groups that contributed to the synthesis of unnatural derivatives of pancratistatin, see ref. 15d
    • Y.-G. Jung H.-U. Kang H.-K. Cho C.-G. Cho Org. Lett. 2011 13 5890 5892
    • (2011) Org. Lett. , vol.13 , pp. 5890-5892
    • Jung, Y.-G.1    Kang, H.-U.2    Cho, H.-K.3    Cho, C.-G.4
  • 17
    • 26844546931 scopus 로고    scopus 로고
    • The cis-fused C10b epimers of 1-deoxypancratistatin and of 1,7-deoxypancratistatin were shown to be inactive
    • J. McNulty V. Larichev S. Pandey Bioorg. Med. Chem. Lett. 2005 15 5315 5318
    • (2005) Bioorg. Med. Chem. Lett. , vol.15 , pp. 5315-5318
    • McNulty, J.1    Larichev, V.2    Pandey, S.3
  • 44
    • 37649017919 scopus 로고    scopus 로고
    • The stereochemical details of the IMDAF cycloaddition would be addressed in a forthcoming paper For the IMDAF cycloaddition of (non-halogenated) tertiary acrylamides, see
    • R. N. Ram N. Kumar Tetrahedron Lett. 2008 49 799 802
    • (2008) Tetrahedron Lett. , vol.49 , pp. 799-802
    • Ram, R.N.1    Kumar, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.