메뉴 건너뛰기




Volumn 17, Issue 13, 2011, Pages 3593-3597

The catalytic ability of various transition metals in the direct functionalization of aromatic C-H bonds

Author keywords

aryl bromide; biaryls; C H activation; cross coupling; transition metal catalysis

Indexed keywords

ARYL BROMIDES; BIARYLS; C-H ACTIVATION; CROSS-COUPLINGS; TRANSITION-METAL CATALYSIS;

EID: 79952593096     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002309     Document Type: Article
Times cited : (78)

References (99)
  • 6
    • 33947493717 scopus 로고    scopus 로고
    • R. G. Bergman, Nature 2007, 446, 391-393
    • (2007) Nature , vol.446 , pp. 391-393
    • Bergman, R.G.1
  • 10
    • 67649488045 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 5094-5115
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5094-5115
  • 12
    • 72449170089 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9792-9826
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9792-9826
  • 18
    • 18844405201 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3125-3129
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 3125-3129
  • 24
    • 38849126856 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 1115-1118
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1115-1118
  • 30
    • 21244438753 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4046-4048
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4046-4048
  • 32
    • 35648969183 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 7996-8000
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 7996-8000
  • 35
    • 70349921519 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6713-6716.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6713-6716
  • 37
    • 70349783659 scopus 로고    scopus 로고
    • references therein.
    • Angew. Chem. Int. Ed. 2009, 48, 3999-4001, and references therein.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3999-4001
  • 39
    • 59849129287 scopus 로고    scopus 로고
    • references therein.
    • M. Li, R. Hua, Tetrahedron Lett. 2009, 50, 1478-1481, and references therein.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 1478-1481
    • Li, M.1    Hua, R.2
  • 45
    • 70349784952 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 3296-3300
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3296-3300
  • 48
    • 34250844398 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 3135-3138
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 3135-3138
  • 50
    • 70349779001 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6045-6048
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6045-6048
  • 52
    • 79952613904 scopus 로고    scopus 로고
    • For selected examples of cross-coupling reactions involving the functionalization of C-H bonds catalyzed by transition metals of the first row, see
    • For selected examples of cross-coupling reactions involving the functionalization of C-H bonds catalyzed by transition metals of the first row, see
  • 54
    • 33745694711 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 1276-1279
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1276-1279
  • 56
    • 54749149062 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 7497-7500
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 7497-7500
  • 64
    • 21244489719 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3913-3917
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 3913-3917
  • 66
    • 34548356423 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 6505-6507
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 6505-6507
  • 68
    • 36749002068 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 8862-8865
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 8862-8865
  • 71
    • 57349174599 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 8897-8900
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8897-8900
  • 74
    • 70349786341 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 3817-3820
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3817-3820
  • 77
    • 77949383639 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 2004-2008
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2004-2008
  • 80
    • 34548356420 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 6518-6520.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 6518-6520
  • 84
    • 47249136281 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 2089-2092
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 2089-2092
  • 88
    • 77949587544 scopus 로고    scopus 로고
    • references therein.
    • G. Cahiez, A. Moyeux, Chem. Rev. 2010, 110, 1435-1462, and references therein.
    • (2010) Chem. Rev. , vol.110 , pp. 1435-1462
    • Cahiez, G.1    Moyeux, A.2
  • 89
    • 79952608664 scopus 로고    scopus 로고
    • For the optimization tables, see the Supporting Information.
    • For the optimization tables, see the Supporting Information.
  • 90
    • 79952591174 scopus 로고    scopus 로고
    • The C-Cl bond could also be tolerated in the coupling of 1-bromo-4-chlorobenzene with benzene, but the yields were relatively lower: for niobium catalysis, 11 %; for molybdenum catalysis, 35 %; for cobalt catalysis, the reaction was complicated.
    • The C-Cl bond could also be tolerated in the coupling of 1-bromo-4-chlorobenzene with benzene, but the yields were relatively lower: for niobium catalysis, 11 %; for molybdenum catalysis, 35 %; for cobalt catalysis, the reaction was complicated.
  • 91
    • 79952580001 scopus 로고    scopus 로고
    • 19F NMR spectra of the mixture of isomeric products, see the Supporting Information.
    • 19F NMR spectra of the mixture of isomeric products, see the Supporting Information.
  • 93
    • 79952603092 scopus 로고    scopus 로고
    • Very recently, two similar works on the arylation of benzene with aryl halides in the presence of catalytic 1,10-phenanthroline derivatives have appeared. However, these reaction systems did not promote the coupling of aryl bromides with benzene at 80 °C. For details, see
    • Very recently, two similar works on the arylation of benzene with aryl halides in the presence of catalytic 1,10-phenanthroline derivatives have appeared. However, these reaction systems did not promote the coupling of aryl bromides with benzene at 80 °C. For details, see
  • 98
    • 70349783568 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 5586-5587.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5586-5587
  • 99
    • 79952609312 scopus 로고    scopus 로고
    • For details of ICP-AES and the results of the control experiment, see the Supporting Information.
    • For details of ICP-AES and the results of the control experiment, see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.