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Volumn 71, Issue 1, 1998, Pages 79-82

Efficient Dimerization of Propene by Nickel-Phosphine Catalysis in the Presence of Sulfonic Acids and/or Dialkyl Sulfates. Effects of Phosphine Ligands and Additives

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EID: 0005624826     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.71.79     Document Type: Article
Times cited : (9)

References (23)
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    • (1988) The Organometallic Chemistry of the Transition Metals
    • Crabtree, R.H.1
  • 2
    • 84926121843 scopus 로고
    • D. Reidel Publishing Co., Dortrecht
    • For example, a) R. H. Crabtree, "The Organometallic Chemistry of the Transition Metals," John Wiley & Sons, Inc., New York (1988); b) "Industrial Applications of Homogeneous Catalysis," ed by A. Mortreux and F. Petit, D. Reidel Publishing Co., Dortrecht (1988); c) L. S. Liebeskind, "Advances in Metal-Organic Chemistry," JAI Press Ltd., London (1989), Vol. 1; (1991), Vol. 2.
    • (1988) Industrial Applications of Homogeneous Catalysis
    • Mortreux, A.1    Petit, F.2
  • 3
    • 84926121843 scopus 로고
    • JAI Press Ltd., London
    • For example, a) R. H. Crabtree, "The Organometallic Chemistry of the Transition Metals," John Wiley & Sons, Inc., New York (1988); b) "Industrial Applications of Homogeneous Catalysis," ed by A. Mortreux and F. Petit, D. Reidel Publishing Co., Dortrecht (1988); c) L. S. Liebeskind, "Advances in Metal-Organic Chemistry," JAI Press Ltd., London (1989), Vol. 1; (1991), Vol. 2.
    • (1989) Advances in Metal-Organic Chemistry , vol.1-2
    • Liebeskind, L.S.1
  • 6
    • 0004029968 scopus 로고
    • Academic Press, London
    • For example, a) P. W. Jolly and G. Wilke, "The Organic Chemistry of Nickel," Academic Press, London (1974); b) S. M. Pillai, M. Ravindranathan, and S. Sivaram, Chem. Rev., 86, 353 (1986).
    • (1974) The Organic Chemistry of Nickel
    • Jolly, P.W.1    Wilke, G.2
  • 7
    • 0012989258 scopus 로고
    • For example, a) P. W. Jolly and G. Wilke, "The Organic Chemistry of Nickel," Academic Press, London (1974); b) S. M. Pillai, M. Ravindranathan, and S. Sivaram, Chem. Rev., 86, 353 (1986).
    • (1986) Chem. Rev. , vol.86 , pp. 353
    • Pillai, S.M.1    Ravindranathan, M.2    Sivaram, S.3
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    • DE 2027831 (1971); DE 2245930 (1973)
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    • Bullard, H.L.1
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    • 0011463123 scopus 로고
    • Previous works: a) H. Sato, T. Noguchi, and S. Yasui, Bull. Chem. Soc. Jpn., 66, 3069 (1993); b) H. Sato and H. Tojima, Bull. Chem. Soc. Jpn., 66, 3079 (1993).
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    • Sato, H.1    Noguchi, T.2    Yasui, S.3
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    • Previous works: a) H. Sato, T. Noguchi, and S. Yasui, Bull. Chem. Soc. Jpn., 66, 3069 (1993); b) H. Sato and H. Tojima, Bull. Chem. Soc. Jpn., 66, 3079 (1993).
    • (1993) Bull. Chem. Soc. Jpn. , vol.66 , pp. 3079
    • Sato, H.1    Tojima, H.2
  • 20
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    • As demonstrated previously, 2,3-dimethyl-2-butene with high purity (>99%) could be obtained by a fractional distillation from the reaction solution. 2,3-Dimethyl-1-butene with high purity could also be obtained in the same manner: H. Sato, M. Ohsu, and Y. Kumagai, J. Synth. Org. Chem. Jpn., 48, 806 (1990).
    • (1990) J. Synth. Org. Chem. Jpn. , vol.48 , pp. 806
    • Sato, H.1    Ohsu, M.2    Kumagai, Y.3
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    • note
    • 3 might be different. The accurate order based on the propene reacted might be thus difficult among these catalyst systems.


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