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Volumn 126, Issue 33, 2004, Pages 10264-10266

Ah intramolecular Diels-Alder approach to the eunicelins: Enantioselective total synthesis of ophirin B

Author keywords

[No Author keywords available]

Indexed keywords

ASBESTININ; BRIARELLIN; DITERPENE; EUNICELIN; OPHIRIN B; UNCLASSIFIED DRUG; EUNICELLIN;

EID: 4143082644     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja046574b     Document Type: Article
Times cited : (71)

References (44)
  • 4
    • 0001401483 scopus 로고
    • (d) Coll, J. C. Chem. Rev. 1992, 92, 613-631.
    • (1992) Chem. Rev. , vol.92 , pp. 613-631
    • Coll, J.C.1
  • 22
    • 4143060460 scopus 로고    scopus 로고
    • note
    • (6Z)-3,14,18-triacetoxycladiella-6,11-diene. This structure was not given a trivial name in the original isolation paper. Because it is the 6,7-Z isomer of ophirin, we have adopted the trivial name of ophirin B for convenience.
  • 42
    • 4143090595 scopus 로고    scopus 로고
    • note
    • Use of the free alcohol or a benzyl ether as protecting group for the C3 hydroxyl resulted in significantly reduced diastereoselectivity and slower rates of reaction for the cycloaddition.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.