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Volumn 41, Issue 6, 2000, Pages 911-914

Synthesis of marine sesterterpenoid dysidiolide

Author keywords

Antitumour compounds; Marine metabolites; Natural products; Terpenes; Terpenoids

Indexed keywords

ANTINEOPLASTIC AGENT; CELL CYCLE PROTEIN; DYSIDIOLIDE; PHOSPHOPROTEIN PHOSPHATASE INHIBITOR; SESTERTERPENE; TERPENE DERIVATIVE;

EID: 0034606978     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)02175-9     Document Type: Article
Times cited : (39)

References (16)
  • 2
    • 0001655988 scopus 로고    scopus 로고
    • Recently cladocorans A and B, having the same carbon skeleton, were reported. Fontana, A.; Ciavatta, M. L.; Cimino, G. J. Org. Chem. 1998, 63, 2845-2849.
    • (1998) J. Org. Chem. , vol.63 , pp. 2845-2849
    • Fontana, A.1    Ciavatta, M.L.2    Cimino, G.3
  • 9
    • 0343020854 scopus 로고    scopus 로고
    • note
    • 3P, THF, r.t.
  • 10
    • 0343892210 scopus 로고    scopus 로고
    • note
    • The relative configuration of alcohols 5a and 5b was determined from the NOESY spectrum of decalin 8, which was derived from 5a and 5b, respectively.
  • 12
    • 0343892209 scopus 로고    scopus 로고
    • note
    • The relative configuration of decalin 8 was determined by the NOESY spectrum. (Equation Presented)
  • 13
    • 0343456479 scopus 로고    scopus 로고
    • note
    • The relative configuration of compound 11 was determined by the NOESY spectrum of compound iii, which was converted from compound 11. (Equation Presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.