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Volumn 17, Issue 46, 2011, Pages 12886-12890

Room-temperature synthesis of tetra-ortho-substituted biaryls by NHC-catalyzed Suzuki-Miyaura couplings

Author keywords

biaryls; cross coupling; N heterocyclic carbene ligand; palladium

Indexed keywords

ARYL BROMIDES; BIARYLS; CATALYTIC PERFORMANCE; CROSS-COUPLINGS; DFT CALCULATION; N-HETEROCYCLIC CARBENE LIGANDS; ROOM TEMPERATURE; ROOM TEMPERATURE SYNTHESIS; SIDE-CHAINS; SUZUKI-MIYAURA COUPLING;

EID: 80555144134     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201102442     Document Type: Article
Times cited : (86)

References (54)
  • 1
    • 20544450502 scopus 로고    scopus 로고
    • 2 nd ed. (Eds.: A. de Meijere, F. Diederich), Wiley-VCH, Weinheim.
    • See the Supporting Information for details.: Metal-Catalyzed Cross-Coupling Reactions, 2 nd ed., (Eds.: A. de Meijere, F. Diederich,), Wiley-VCH, Weinheim, 2004.
    • (2004) Metal-Catalyzed Cross-Coupling Reactions
  • 15
    • 84890973385 scopus 로고    scopus 로고
    • (Ed.: L. Ackermann), Wiley-VCH, Weinheim.
    • Modern Arylation Methods (Ed.:, L. Ackermann,), Wiley-VCH, Weinheim, 2009.
    • (2009) Modern Arylation Methods
  • 27
    • 11444254369 scopus 로고    scopus 로고
    • For two examples of Kumada couplings at elevated temperatures, see
    • For efficient tetra-ortho-substituted biaryl formation starting from aryl bromides with appropriate heating, see references [4a, d, e, h]. For two examples of Stille couplings at elevated temperatures, see: W. Su, S. Urgaonkar, P. A. McLaughlin, J. G. Verkade, J. Am. Chem. Soc. 2004, 126, 16433. For two examples of Kumada couplings at elevated temperatures, see
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 16433
    • Su, W.1    Urgaonkar, S.2    McLaughlin, P.A.3    Verkade, J.G.4
  • 28
    • 66149142155 scopus 로고    scopus 로고
    • For two examples of Negishi couplings at elevated temperature, see
    • C. E. Hartmann, S. P. Nolan, C. S. J. Cazin, Organometallics 2009, 28, 2915. For two examples of Negishi couplings at elevated temperature, see
    • (2009) Organometallics , vol.28 , pp. 2915
    • Hartmann, C.E.1    Nolan, S.P.2    Cazin, C.S.J.3
  • 29
    • 5644254180 scopus 로고    scopus 로고
    • For a series of examples of Negishi couplings that proceed at room temperature or slightly above, underlining the higher reactivity compared to Suzuki-Miyaura couplings, see
    • J. E. Milne, S. L. Buchwald, J. Am. Chem. Soc. 2004, 126, 13028. For a series of examples of Negishi couplings that proceed at room temperature or slightly above, underlining the higher reactivity compared to Suzuki-Miyaura couplings, see
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 13028
    • Milne, J.E.1    Buchwald, S.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.