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Volumn 52, Issue 17, 2011, Pages 2072-2075

Stereoselective synthesis of the decahydrofluorene core of the hirsutellones

Author keywords

Hirsutellone B; Intramolecular Diels Alder reaction; Oxonium ion activated dienophile; Siloxacyclopentene constrained dienophile; Stereoselective synthesis

Indexed keywords

DECAHYDROFLUORENE CORE; POLYKETIDE; UNCLASSIFIED DRUG;

EID: 79953199725     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.10.111     Document Type: Article
Times cited : (28)

References (26)
  • 6
    • 0003009874 scopus 로고
    • Reviews of intramolecular Diels-Alder reactions: (a)
    • Reviews of intramolecular Diels-Alder reactions: (a) Ciganek, B. Org. React. 1983, 32, 1;
    • (1983) Org. React. , vol.32 , pp. 1
    • Ciganek, B.1
  • 8
    • 0000048482 scopus 로고
    • Trost, B. M., Ed.; Pergamon Press: Oxford
    • (c) Roush, W. R. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon Press: Oxford, 1991; Vol. 5, pp 513-550;
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513-550
    • Roush, W.R.1
  • 17
    • 79953232098 scopus 로고    scopus 로고
    • note
    • 3P, and contains ca. 15% of the (Z)-isomer which we were unable to separate. Therefore, the 85:15 mixture of isomeric phosphonium salts was used in the Wittig reaction. The corresponding mixture of triene isomers produced at the stage of 8 could not be separated at any stage of this synthesis.
  • 24
    • 79953205027 scopus 로고    scopus 로고
    • note
    • The siloxacyclopentene unit of the cycloadduct derived from 1 was unstable and could not be isolated.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.