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Volumn 8, Issue 25, 2006, Pages 5901-5904

Exploring biosynthetic relationships among furanocembranoids: Synthesis of (-)-bipinnatin J, (H-)-intricarene, (+)-rubifolide, and (+)-isoepilophodione B

Author keywords

[No Author keywords available]

Indexed keywords

BIPINNATIN J; DITERPENE; INTRICARENE; ISOEPILOPHODIONE B; RUBIFOLIDE; TRITERPENE; UNCLASSIFIED DRUG;

EID: 33846325856     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol062581o     Document Type: Article
Times cited : (108)

References (29)
  • 7
    • 33846306493 scopus 로고    scopus 로고
    • Avrainvillamide, a Cytotoxic Marine Natural Product, and Derivatives thereof
    • U.S. Patent 6,066,635
    • (c) Fenical, W.; Jensen, P. R.; Cheng, X. C. Avrainvillamide, a Cytotoxic Marine Natural Product, and Derivatives thereof. U.S. Patent 6,066,635, 2000.
    • (2000)
    • Fenical, W.1    Jensen, P.R.2    Cheng, X.C.3
  • 28
    • 0030796165 scopus 로고    scopus 로고
    • For previous synthesis of, -rubifolide see
    • For previous synthesis of (-)-rubifolide see: Marshall, J. A.; Sehon, C. A. J. Org. Chem. 1997, 62, 4313-4320.
    • (1997) J. Org. Chem , vol.62 , pp. 4313-4320
    • Marshall, J.A.1    Sehon, C.A.2
  • 29
    • 33846282864 scopus 로고    scopus 로고
    • In Pattenden's work (ref 9), intricarene was obtained from 24 in 10% yield under the DBU/MeCN conditions. However, this was not optimized due to the relative dearth of bipinnatin J available.
    • In Pattenden's work (ref 9), intricarene was obtained from 24 in 10% yield under the DBU/MeCN conditions. However, this was not optimized due to the relative dearth of bipinnatin J available.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.