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Volumn , Issue 4, 2006, Pages 420-422

Enantioselective total synthesis of (-)-flustramines A, B and (-)-flustramides A, B via domino olefination/isomerization/Claisen rearrangement sequence

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; FLUSTRAMIDE A; FLUSTRAMIDE B; FLUSTRAMINE A; FLUSTRAMINE B; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33645454637     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b512485a     Document Type: Article
Times cited : (62)

References (41)
  • 38
    • 33645453155 scopus 로고    scopus 로고
    • When alane-reduction of 15 at room temperature was carried out, flustramine B (2) was directly obtained, but the yield was low (34%) All spectra of the synthetic products 1-4 agreed with those of isolated products 1-3 and synthetic materials in racemic form, 12 respectively
    • Oxidative fission produced an unstable aldehyde, which was used without further purification in the next reaction
  • 41
    • 33645459030 scopus 로고    scopus 로고
    • The tentative assignment of the stereochemistry was based on consideration of transition state in Claisen rearrangement, and comparison of the specific rotations of the reverse-prenyl series with that of the prenyl version
    • The tentative assignment of the stereochemistry was based on consideration of transition state in Claisen rearrangement, and comparison of the specific rotations of the reverse-prenyl series with that of the prenyl version


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.