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Volumn 65, Issue 37, 2009, Pages 7784-7789

Convergent synthesis of the A-E ring segment of ciguatoxin CTX3C

Author keywords

Ciguatoxin; Intramolecular allylation; Polycyclic ethers; Ring closing metathesis

Indexed keywords

ALPHA CHLOROATOXY ETHER; CIGUATOXIN; ETHER DERIVATIVE; UNCLASSIFIED DRUG;

EID: 68249123501     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.07.037     Document Type: Article
Times cited : (19)

References (32)
  • 4
  • 6
    • 68249110845 scopus 로고    scopus 로고
    • For recent reviews on syntheses of polycyclic ethers, see
    • For recent reviews on syntheses of polycyclic ethers, see:
  • 7
    • 30744459350 scopus 로고    scopus 로고
    • Nakata T. Chem. Rev. 105 (2005) 4314-4347
    • (2005) Chem. Rev. , vol.105 , pp. 4314-4347
    • Nakata, T.1
  • 8
    • 30744476469 scopus 로고    scopus 로고
    • Inoue M. Chem. Rev. 105 (2005) 4379-4405
    • (2005) Chem. Rev. , vol.105 , pp. 4379-4405
    • Inoue, M.1
  • 12
    • 68249110054 scopus 로고    scopus 로고
    • For the previous synthesis of the A-E ring segment of 1, see:
    • For the previous synthesis of the A-E ring segment of 1, see:
  • 22
    • 68249110309 scopus 로고    scopus 로고
    • note
    • Compounds 14 and 15 were the products isolated in reasonable yields, and the other stereoisomer was not detected.
  • 23
    • 68249098529 scopus 로고    scopus 로고
    • note
    • 4 in MeOH afforded the undesired isomer 15 as a major product.
  • 27
    • 68249089891 scopus 로고    scopus 로고
    • For the original conditions, see
    • For the original conditions, see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.