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Volumn , Issue 5, 2011, Pages 689-693

An approach to highly functionalized quinolines and isoquinolines via a gold-catalyzed benzannulation

Author keywords

benzannulation; catalysis; gold; isoquinolines; quinolines

Indexed keywords

ALKYNE DERIVATIVE; GOLD CHLORIDE; ISOQUINOLINE DERIVATIVE; OXO ALKYNE DERIVATIVE; PYRIDINE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79952455324     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1259555     Document Type: Article
Times cited : (13)

References (36)
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    • During the course of our work Organ et al. reported a few reactions of pyridine-containing oxo-alkynes in a flow reactor under heterogeneous conditions, see:; doi: 10.3762/bjoc.5.35
    • During the course of our work Organ et al. reported a few reactions of pyridine-containing oxo-alkynes in a flow reactor under heterogeneous conditions, see:, Shore G, Tsimerman M, Organ M G., Beilstein J. Org. Chem. 2009 5 35; doi: 10.3762/bjoc.5.35
    • (2009) Beilstein J. Org. Chem. , vol.5 , pp. 35
    • Shore, G.1    Tsimerman, M.2    Organ, M.G.3
  • 20
    • 0003607021 scopus 로고
    • In Katritzky A. R. Rees C. W. Pergamon New York Chap. 2.09
    • Yates F S., In Comprehensive Heterocyclic Chemistry Vol. 2 Katritzky A R. Rees C W. Pergamon New York 1984 Chap. 2.09
    • (1984) Comprehensive Heterocyclic Chemistry , vol.2
    • Yates, F.S.1
  • 23
    • 79952451216 scopus 로고    scopus 로고
    • For recent reports on isoquinoline synthesis, see
    • For recent reports on isoquinoline synthesis, see
  • 35
    • 4344590797 scopus 로고    scopus 로고
    • For a discussion and computational analysis regarding [3+2] vs. [4+2] cycloaddition of isobenzopyrylium 1,3-dipoles, see
    • For a discussion and computational analysis regarding [3+2] vs. [4+2] cycloaddition of isobenzopyrylium 1,3-dipoles, see:, Straub B F., Chem. Commun. 2004 1726
    • (2004) Chem. Commun. , pp. 1726
    • Straub, B.F.1
  • 36
    • 11144290815 scopus 로고    scopus 로고
    • We also cannot rule out the possibility of autocatalysis by the oxo-alkynes, as sometimes substrates might coordinate and lead to the formation of even more efficient catalysts, see
    • We also cannot rule out the possibility of autocatalysis by the oxo-alkynes, as sometimes substrates might coordinate and lead to the formation of even more efficient catalysts, see:, Hashmi A S. K., Weyrauch J P., Rudolph M, Kurpejovic E, Angew. Chem. Int. Ed. 2004 43 6545
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 6545
    • Hashmi, A.S.K.1    Weyrauch, J.P.2    Rudolph, M.3    Kurpejovic, E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.