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Volumn 78, Issue 16, 2013, Pages 8169-8175

Direct arylation of oligonaphthalenes using PIFA/BF3· Et2O: From double arylation to larger oligoarene products

Author keywords

[No Author keywords available]

Indexed keywords

ARYLATIONS; C-H BOND; CROSS-COUPLINGS; DEHYDROGENATIVE COUPLING; SELECTIVE FUNCTIONALIZATION; SUBSTITUTED BENZENES;

EID: 84882346856     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo401001k     Document Type: Article
Times cited : (18)

References (20)
  • 6
    • 69249101991 scopus 로고    scopus 로고
    • A selection of examples where a directing tether was used in Ar-Ar coupling can be found in: McGlacken, G. P.; Bateman, L. M. Chem. Soc. Rev. 2009, 38, 2447
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2447
    • McGlacken, G.P.1    Bateman, L.M.2
  • 9
    • 34248529661 scopus 로고    scopus 로고
    • An alternative mechanism for what may appear to be CH arylation has also been identified, see: Sánchez, R. S.; Zhuravlev, F. A. J. Am. Chem. Soc. 2007, 129, 5824
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5824
    • Sánchez, R.S.1    Zhuravlev, F.A.2
  • 14
    • 84882411143 scopus 로고    scopus 로고
    • Organic EL Light Emitting Element. JP 2005,019219 (A), Jan 20
    • 4 has been previously accessed at Sony Corp. via Ni-catalyzed Kumada coupling: Takada, K.; Sakamoto, H.; Ichimura, M.; Tamura, S. Organic EL Light Emitting Element. JP 2005,019219 (A), Jan 20, 2005.
    • (2005)
    • Takada, K.1    Sakamoto, H.2    Ichimura, M.3    Tamura, S.4
  • 17
    • 0002773030 scopus 로고
    • A slow interconversion is consistent with a ∼23 kcal/mol racemization/rotation barrier in 1,1′-binaphthalene: Cooke, A. S.; Harris, M. M. J. Chem. Soc. 1963, 2365
    • (1963) J. Chem. Soc. , pp. 2365
    • Cooke, A.S.1    Harris, M.M.2
  • 18
    • 0000718373 scopus 로고    scopus 로고
    • Pu, L. Chem. Rev. 1998, 98, 2405
    • (1998) Chem. Rev. , vol.98 , pp. 2405
    • Pu, L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.