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Volumn 13, Issue 7, 2011, Pages 1750-1753

Metal-free halonium mediated acetate shifts of ynamides to access α-halo acrylamides/acrylimides

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EID: 79953186956     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200269h     Document Type: Article
Times cited : (26)

References (53)
  • 15
    • 0000365487 scopus 로고    scopus 로고
    • For a review of transition-metal-catalyzed cross-coupling, see
    • For a review of transition-metal-catalyzed cross-coupling, see: Negishi, E. J. Organomet. Chem. 1999, 576, 179
    • (1999) J. Organomet. Chem. , vol.576 , pp. 179
    • Negishi, E.1
  • 27
    • 79953205824 scopus 로고    scopus 로고
    • Most likely to generate the more reactive allenyl acetates in situ. Referrence 5b.
    • Most likely to generate the more reactive allenyl acetates in situ. Referrence 5b.
  • 50
    • 79953191345 scopus 로고    scopus 로고
    • N -Fluorobenzenesulfonimide.
    • N -Fluorobenzenesulfonimide.
  • 51
    • 79953177395 scopus 로고    scopus 로고
    • See Supporting Information for the optimization.
    • See Supporting Information for the optimization.
  • 52
    • 79953188953 scopus 로고    scopus 로고
    • The Z -configuration was confirmed by the proton-fluorine coupling constant.
    • The Z -configuration was confirmed by the proton-fluorine coupling constant.
  • 53
    • 79953170117 scopus 로고    scopus 로고
    • A concerted [3,3]-rearrangement of 5 would also explain the stereochemical outcome.
    • A concerted [3,3]-rearrangement of 5 would also explain the stereochemical outcome.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.