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Volumn 3, Issue 17, 2001, Pages 2749-2752

Stereoselective syntheses of the C′D′E′F′-ring system of maitotoxin and the FG-ring system of gambierol

Author keywords

[No Author keywords available]

Indexed keywords

CIGUATOXIN; ETHER DERIVATIVE; GAMBIEROL; MAITOTOXIN; MARINE TOXIN; OXOCIN DERIVATIVE; POLYCYCLIC HYDROCARBON;

EID: 0035940131     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016355k     Document Type: Article
Times cited : (61)

References (52)
  • 35
    • 0001343212 scopus 로고
    • For reviews, see: (a) Kagan, H. B. New J. Chem. 1990, 14, 453.
    • (1990) New J. Chem. , vol.14 , pp. 453
    • Kagan, H.B.1
  • 38
    • 0034699855 scopus 로고    scopus 로고
    • A stepwise construction of 1,3-diaxial angular methyl groups on a tetrahydropyran was reported in a synthesis of the F-ring of gambierol. (a) Fuwa, H.; Sasaki, M.; Tachibana, K. Tetrahedron Lett. 2000, 41, 8371.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 8371
    • Fuwa, H.1    Sasaki, M.2    Tachibana, K.3
  • 44
    • 0041294181 scopus 로고    scopus 로고
    • note
    • 24 using styrylepoxide. Thus, the Nicolaou procedure was applied to the construction of the E′-ring system.
  • 52
    • 0042796916 scopus 로고    scopus 로고
    • note
    • The acetate derivative of 15 showed coupling constants (7.3 and 6.8 Hz) significantly different from the typical values.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.