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Volumn 11, Issue 9, 2013, Pages 1456-1459

Indium-catalyzed annulation of 3-aryl- and 3-heteroarylindoles with propargyl ethers: Synthesis and photoluminescent properties of aryl- and heteroaryl[c]carbazoles

Author keywords

[No Author keywords available]

Indexed keywords

ETHERS; INDIUM; POLYCYCLIC AROMATIC HYDROCARBONS;

EID: 84875871230     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob27407a     Document Type: Article
Times cited : (30)

References (33)
  • 17
    • 70349653362 scopus 로고    scopus 로고
    • For Bergman's method capable of providing five [a]-types and nine [c]-types on indolyl-annulated carbazoles, see
    • Z. Shi S. Ding Y. Cui N. Jiao Angew. Chem., Int. Ed. 2009 48 7895
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 7895
    • Shi, Z.1    Ding, S.2    Cui, Y.3    Jiao, N.4
  • 21
    • 0033582452 scopus 로고    scopus 로고
    • For Nagarajan's method capable of providing one [a]-type and seven [c]-types on pyrido-annulated carbazoles via the Povarov reaction, see
    • T. Janosik J. Bergman Tetrahedron 1999 55 2371
    • (1999) Tetrahedron , vol.55 , pp. 2371
    • Janosik, T.1    Bergman, J.2
  • 22
    • 84855658156 scopus 로고    scopus 로고
    • For Queiroz's method capable of providing one [a]-type and three [c]-types on thienyl-annulated carbazoles, see
    • M. Viji R. Nagarajan Synthesis 2012 253
    • (2012) Synthesis , pp. 253
    • Viji, M.1    Nagarajan, R.2
  • 26
    • 33947158483 scopus 로고    scopus 로고
    • For Gribble's method capable of providing one [a]-type and one [c]-type on phenyl-annulated carbazoles, see
    • M. Yamamoto S. Matsubara Chem. Lett. 2007 36 172
    • (2007) Chem. Lett. , vol.36 , pp. 172
    • Yamamoto, M.1    Matsubara, S.2
  • 27
    • 0033010027 scopus 로고    scopus 로고
    • For de Koning's method capable of providing two [a]-types and two [c]-types on naphthyl- and phenyl-annulated carbazoles, see
    • G. W. Gribble R. A. Silva M. G. Saulnier Synth. Commun. 1999 29 729
    • (1999) Synth. Commun. , vol.29 , pp. 729
    • Gribble, G.W.1    Silva, R.A.2    Saulnier, M.G.3
  • 29
    • 0026641809 scopus 로고
    • Results on the effect of other Lewis acid catalysts examined under the conditions shown in entry 1 are as follows: In(NTf2)3 (23%, >99:1), In(OTf)3 (35%, 99:1), InCl3 (<1%), AuCl3/3AgOTf (6%, 97:3), Cu(OTf)2 (1%, 92:8), Bi(OTf) 3 (4%, 94:6), Zn(OTf)2 (<1%). Tf = SO 2CF3 A phenyl group on a nitrogen atom of an indole has reportedly participated in a palladium-catalyzed annulation using alkynes, see
    • R. F. C. Brown K. J. Coulston F. W. Eastwood M. R. Moffat Tetrahedron 1992 48 7763
    • (1992) Tetrahedron , vol.48 , pp. 7763
    • Brown, R.F.C.1    Coulston, K.J.2    Eastwood, F.W.3    Moffat, M.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.