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Volumn 75, Issue 24, 2010, Pages 8478-8486

Expedient synthesis of a stereoisomer of acremolide B

Author keywords

[No Author keywords available]

Indexed keywords

CROSS METATHESIS; DIPEPTIDE; MACROLIDE CORE; STEREO-SELECTIVE; STEREOGENIC CENTERS; STRAIGHTFORWARD STRATEGY;

EID: 78650364953     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1017487     Document Type: Article
Times cited : (15)

References (24)
  • 11
    • 78650333975 scopus 로고    scopus 로고
    • 3)}
    • 3)}.
  • 20
    • 78650328214 scopus 로고    scopus 로고
    • 2 afforded the desired compound in a slightly lower yield (60%)
    • 2 afforded the desired compound in a slightly lower yield (60%).
  • 22
    • 78650406190 scopus 로고    scopus 로고
    • 13C NMR spectra of both the natural and the synthetic acremolide B, it is particularly difficult to speculate on the relative and absolute configuration of the C2, C3, C5, and C6 stereogenic centers (see Supporting Information for comparative Table), not to mention that, due to the cyclic nature of the natural product, a slight modification of one of the stereogenic centers could have a tremendous impact on the overall configuration of the molecule and therefore on all the chemical shifts
    • 13C NMR spectra of both the natural and the synthetic acremolide B, it is particularly difficult to speculate on the relative and absolute configuration of the C2, C3, C5, and C6 stereogenic centers (see Supporting Information for comparative Table), not to mention that, due to the cyclic nature of the natural product, a slight modification of one of the stereogenic centers could have a tremendous impact on the overall configuration of the molecule and therefore on all the chemical shifts.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.