메뉴 건너뛰기




Volumn , Issue 8, 2011, Pages 1467-1471

Room-temperature nickel-catalysed Suzuki-Miyaura reactions of aryl sulfonates/halides with arylboronic acids

Author keywords

Boron; Cross coupling; Halides; Nickel; Phosphane ligands

Indexed keywords


EID: 79952161680     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001519     Document Type: Article
Times cited : (65)

References (57)
  • 1
    • 79952178016 scopus 로고    scopus 로고
    • For selected reviews on Pd-catalysed Suzuki-Miyaura reactions, see
    • For selected reviews on Pd-catalysed Suzuki-Miyaura reactions, see
  • 10
    • 79952179949 scopus 로고    scopus 로고
    • For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of haloarenes using the chloride, see
    • For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of haloarenes using the chloride, see
  • 21
    • 79952148569 scopus 로고    scopus 로고
    • For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of aryl sulfonates (OTs, OBs, OMs), see
    • For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of aryl sulfonates (OTs, OBs, OMs), see
  • 26
    • 79952133125 scopus 로고    scopus 로고
    • For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of other electrophiles containing unusual leaving groups using aryl carboxylates, see
    • For Ni-catalysed Suzuki-Miyaura aryl-aryl coupling reactions of other electrophiles containing unusual leaving groups using aryl carboxylates, see
  • 33
    • 70349970582 scopus 로고    scopus 로고
    • using aryl methyl ether, see
    • Angew. Chem. Int. Ed. 2009, 48, 3569-3571, using aryl methyl ether, see
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3569-3571
  • 35
    • 50049090202 scopus 로고    scopus 로고
    • using aryl nitriles, see
    • Angew. Chem. Int. Ed. 2008, 47, 4866-4869, using aryl nitriles, see
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4866-4869
  • 40
    • 79952130054 scopus 로고    scopus 로고
    • For selected Ni heterogeneously catalysed Suzuki-Miyaura aryl-aryl coupling reactions, see
    • For selected Ni heterogeneously catalysed Suzuki-Miyaura aryl-aryl coupling reactions, see
  • 43
    • 79952136053 scopus 로고    scopus 로고
    • For room-temperature Suzuki-Miyaura aryl-aryl coupling reactions catalysed by nickel catalysts, see
    • For room-temperature Suzuki-Miyaura aryl-aryl coupling reactions catalysed by nickel catalysts, see
  • 49
    • 84858627234 scopus 로고
    • II-(σ-aryl) complexes as catalysts in the cyanation of bromothiophenes, see
    • II-(σ-aryl) complexes as catalysts in the cyanation of bromothiophenes, see:, J. V. Soolinger, H. D. Verkruijsse, M. A. Keegstra, L. Brandsma, Synth. Commun. 1990, 20, 3153-3156.
    • (1990) Synth. Commun. , vol.20 , pp. 3153-3156
    • Soolinger, J.V.1    Verkruijsse, H.D.2    Keegstra, M.A.3    Brandsma, L.4
  • 50
    • 79952132450 scopus 로고    scopus 로고
    • [3f,4d]
    • [3f,4d]
  • 54
    • 79952129719 scopus 로고    scopus 로고
    • For the preparation of trans-haloarylbis(triphenylphosphane)nickel(II), see
    • For the preparation of trans-haloarylbis(triphenylphosphane)nickel(II), see
  • 55
    • 0016359350 scopus 로고
    • in: (Eds.:, American Chemiscal Society, Washington, DC
    • L. Cassar, S. Ferrara, M. Foá, in: Advances in Chemistry (Eds.:, D. Forster, J. F. Roth), American Chemiscal Society, Washington, DC, 1974, vol. 132, p. 252.
    • (1974) Advances in Chemistry , vol.132 , pp. 252
    • Cassar, L.1    Ferrara, S.2    Foá, M.3    Forster, D.4
  • 57
    • 79952154528 scopus 로고    scopus 로고
    • 2Cl] would be completely converted
    • 2Cl] would be completely converted.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.