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Volumn 6, Issue 1, 2015, Pages 288-293

Stoichiometric to catalytic reactivity of the aryl cycloaurated species with arylboronic acids: Insight into the mechanism of gold-catalyzed oxidative C(sp2)-H arylation

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION ANALYSIS; AROMATIC COMPOUNDS; CATALYSIS; CHEMICAL ACTIVATION; GOLD;

EID: 84918816343     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c4sc02070g     Document Type: Article
Times cited : (63)

References (92)
  • 23
    • 84878520754 scopus 로고    scopus 로고
    • For exceptionally fast aryl-aryl bond reductive elimination from oxidized gold center to form homocoupled products, see
    • M. Hofer C. Nevado Tetrahedron 2013 69 5751
    • (2013) Tetrahedron , vol.69 , pp. 5751
    • Hofer, M.1    Nevado, C.2
  • 39
    • 79957569118 scopus 로고    scopus 로고
    • For selected examples of stoichiometric intermolecular auration of (hetero)arenes with Au(iii) by C-H bond activation, see
    • T. C. Boorman I. Larrosa Chem. Soc. Rev. 2011 40 1910
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 1910
    • Boorman, T.C.1    Larrosa, I.2
  • 54
    • 84886793220 scopus 로고    scopus 로고
    • For selected examples on the palladium-catalyzed C-H bond arylation of arenes with directing groups, see
    • G. Rouquet N. Chatani Angew. Chem., Int. Ed. 2013 52 11726
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 11726
    • Rouquet, G.1    Chatani, N.2
  • 63
  • 92
    • 84902201841 scopus 로고    scopus 로고
    • For optimization of reaction conditions, see Table S1. The pyridyl group of 4ia could be removed to afford 9 in 77% yield. See: L. Ackermann, E. Diers and A. Manvar, Org. Lett., 2012, 14, 1154
    • M. D. Levin F. D. Toste Angew. Chem., Int. Ed. 2014 53 6211
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 6211
    • Levin, M.D.1    Toste, F.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.