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Volumn 133, Issue 28, 2011, Pages 10716-10719

Direct arylation of polycyclic aromatic hydrocarbons through palladium catalysis

Author keywords

[No Author keywords available]

Indexed keywords

ARYLATIONS; C-H BOND; CYCLODEHYDROGENATION; PALLADIUM CATALYSIS;

EID: 79960237702     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja202975w     Document Type: Article
Times cited : (130)

References (44)
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    • Geim, A. K. Science 2009, 324, 1530
    • (2009) Science , vol.324 , pp. 1530
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  • 8
    • 77956505377 scopus 로고    scopus 로고
    • Amplification growth strategy for carbon nanotubes
    • Amplification growth strategy for carbon nanotubes: Fort, E. H.; Scott, L. T. Angew. Chem., Int. Ed. 2010, 49, 6626
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 6626
    • Fort, E.H.1    Scott, L.T.2
  • 15
  • 24
    • 40549087300 scopus 로고    scopus 로고
    • A sole example of C-H bond arylation of PAHs (phenanthrene and fluoranthene)
    • A sole example of C-H bond arylation of PAHs (phenanthrene and fluoranthene): Kawai, H.; Kobayashi, Y.; Oi, S.; Inoue, Y. Chem. Commun. 2008, 1464
    • (2008) Chem. Commun. , pp. 1464
    • Kawai, H.1    Kobayashi, Y.2    Oi, S.3    Inoue, Y.4
  • 25
  • 31
    • 84977699543 scopus 로고
    • EAr reactions) such as bromination are known to occur preferentially at the C1 position of pyrene ring
    • EAr reactions) such as bromination are known to occur preferentially at the C1 position of pyrene ring: Vollmann, H.; Becker, H.; Corell, M.; Streeck, H.; Langbein, G. Liebigs Ann. Chem. 1937, 531, 1
    • (1937) Liebigs Ann. Chem. , vol.531 , pp. 1
    • Vollmann, H.1    Becker, H.2    Corell, M.3    Streeck, H.4    Langbein, G.5
  • 33
    • 0343580709 scopus 로고
    • Oxidation is known to occur at the C4-C5 bond of pyrene ring
    • Oxidation is known to occur at the C4-C5 bond of pyrene ring: Moriarty, R. M.; Dansette, P.; Jerina, D. M. Tetrahedron Lett. 1975, 16, 2557
    • (1975) Tetrahedron Lett. , vol.16 , pp. 2557
    • Moriarty, R.M.1    Dansette, P.2    Jerina, D.M.3
  • 40
    • 79960281319 scopus 로고    scopus 로고
    • The K-region is defined as an exposed outer π-bond of PAHs. In fully benzenoid PAHs where benzene rings are annulated with each other in a "bay region", the added two π-electrons cannot be included in sextet. In fact, these outer π-bonds (K-regions) are less stabilized and possess partial olefinic character, albeit still being aromatic.
    • The K-region is defined as an exposed outer π-bond of PAHs. In fully benzenoid PAHs where benzene rings are annulated with each other in a "bay region", the added two π-electrons cannot be included in sextet. In fact, these outer π-bonds (K-regions) are less stabilized and possess partial olefinic character, albeit still being aromatic.
  • 43
    • 53549128588 scopus 로고    scopus 로고
    • For biphenylative annulation of 1,2-dihalobenzenes through Pd-catalyzed cross-coupling reactions, see: Xue, X.; Scott, L. T. Org. Lett. 2007, 9, 3937
    • (2007) Org. Lett. , vol.9 , pp. 3937
    • Xue, X.1    Scott, L.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.