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Volumn 15, Issue 13, 2013, Pages 3362-3365

Interrupted fischer-indole intermediates via oxyarylation of alkenyl boronic acids

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EID: 84880022812     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol401416r     Document Type: Article
Times cited : (30)

References (57)
  • 1
    • 0012177920 scopus 로고    scopus 로고
    • The Fischer Indole Synthesis
    • Sheldon, R. A. Van Bekkum, H. Wiley-VCH: Weinheim
    • Downing, R. S.; Kunkeler, P. J. The Fischer Indole Synthesis. In Fine Chemicals through Heterogeneous Catalysis; Sheldon, R. A., Van Bekkum, H., Eds.; Wiley-VCH: Weinheim, 2001; pp 178-183.
    • (2001) Fine Chemicals Through Heterogeneous Catalysis , pp. 178-183
    • Downing, R.S.1    Kunkeler, P.J.2
  • 5
    • 0000414271 scopus 로고
    • For a mechanistic study of the Fischer-indole reaction, see: Hughes, D. L.; Zhao, D. J. Org. Chem. 1993, 58, 228
    • (1993) J. Org. Chem. , vol.58 , pp. 228
    • Hughes, D.L.1    Zhao, D.2
  • 7
    • 84864722925 scopus 로고    scopus 로고
    • Mazet, C. Synlett. 2012, 23, 1999
    • (2012) Synlett. , vol.23 , pp. 1999
    • Mazet, C.1
  • 23
    • 84867531243 scopus 로고    scopus 로고
    • For a mechanistic discussion describing the inability to use Pd-catalyzed α-arylation to convert an o -haloaryl amine to an α-(o -aminoaryl)ketone and the inability to use a Buchwald-Hartwig reaction to convert an α-(o -haloaryl)ketone to an α-(o -aminoaryl)ketone, see: Knapp, J. M.; Zhu, J. S.; Tantillo, D. J.; Kurth, M. J. Angew. Chem., Int. Ed. 2012, 51, 10588
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 10588
    • Knapp, J.M.1    Zhu, J.S.2    Tantillo, D.J.3    Kurth, M.J.4
  • 51
    • 0000237802 scopus 로고
    • For a discussion on the limits of regioselectivity in the Fischer-indole reaction, see: Phillips, R. R. Org. React. 1959, 10, 1143 (ref 1d) and references cited therein
    • (1959) Org. React. , vol.10 , pp. 1143
    • Phillips, R.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.