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Volumn 49, Issue , 2003, Pages 167-224

Structure-Reactivity Relationships in the Cyclo-Oligomerization of 1,3-Butadiene Catalyzed by Zerovalent Nickel Complexes

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EID: 0141860687     PISSN: 00653055     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0065-3055(03)49005-9     Document Type: Review
Times cited : (13)

References (102)
  • 1
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    • The oligomerization and co-oligomerization of butadiene and substituted 1,3-dienes
    • (a) P.W Jolly G Wilke The oligomerization and co-oligomerization of butadiene and substituted 1,3-dienes The Organic Chemistry of Nickel. Vol. 2, Organic Synthesis 1975
    • (1975)
    • Jolly, P.W1    Wilke, G2
  • 2
    • 85112876840 scopus 로고
    • Nickel-catalyzed oligomerization of 1,3-dienes related reactions
    • (b) P.W Jolly Nickel-catalyzed oligomerization of 1,3-dienes related reactions Comprehensive Organometallic Chemistry Vol 8 1982
    • (1982)
    • Jolly, P.W1
  • 8
    • 85112947218 scopus 로고    scopus 로고
    • Cyclooligomerizations and cyclo-co-oligomerizations of 1,3-dienes
    • (c) G Wilke A ; Eckerle Cyclooligomerizations and cyclo-co-oligomerizations of 1,3-dienes Applied Homogeneous Catalysis with Organometallic Complexes 1996
    • (1996)
    • Wilke, G1    Eckerle, A3
  • 13
    • 85112888995 scopus 로고    scopus 로고
    • (b) The catalytic cyclodimerization has been performed under the following reaction conditions: 80 °C, normal pressure, and nickel:ligand ratio 1:1
  • 14
    • 85112905207 scopus 로고    scopus 로고
    • (a) A fourth cyclodimer of butadiene, the 1-methylene-2-vinylcyclopentane (MVCP), is formed in the presence of secondary alcohols. The reaction channel that affords this product, however, is not investigated in the present study
  • 18
    • 85112898370 scopus 로고    scopus 로고
    • (c) Kluth J. Ph.D. Thesis, University of Essen-Gesamthochschule, 1980
  • 20
    • 85112941684 scopus 로고    scopus 로고
    • (b) The catalytic cyclotrimerization has been performed under the following conditions: 40–80 °C in liquid butadiene under pressure
  • 24
    • 85112891295 scopus 로고    scopus 로고
    • (c) Tobisch S. Chem. Eur. J. 2003 , 9 , accepted
  • 32
    • 85112927237 scopus 로고    scopus 로고
    • (d) Büssemeier B. Ph.D. Thesis, University of Bochum, 1973
  • 39
    • 85112872391 scopus 로고
    • P Heimbach R Traunmüller Chemie der Metall-Olefin-Komplexe, 1970 Verlag Chemie GmbH Weinheim
    • (1970)
    • Heimbach, P1    Traunmüller, R2
  • 59
    • 85112879579 scopus 로고    scopus 로고
    • 12-cyclo-oligomer reaction channels can be found elsewhere ( Reference 11 )
  • 60
    • 85112943935 scopus 로고    scopus 로고
    • (b) Detailed descriptions of the employed computational methodology are provided elsewhere ( Reference 11 )
  • 61
    • 85112917461 scopus 로고    scopus 로고
    • 3 ligands, the reader is referred to Reference 11b
  • 62
    • 85112875055 scopus 로고    scopus 로고
    • For an overview see the recent special issue Computational Transition Metal Chemistry. Chem. Rev. 2000 , 100 , 351–818
  • 76
    • 85112917421 scopus 로고    scopus 로고
    • (a) F Maseras Computational Organometallic Chemistry 2001
    • (2001)
    • Maseras, F1
  • 79
    • 85112906988 scopus 로고    scopus 로고
    • (a) Full MM3(96) parameter set including π-systems
  • 88
    • 0002610072 scopus 로고
    • Fluxional allyl complexes
    • (b) K Vrieze Fluxional allyl complexes Nuclear Magnetic Resonance Spectroscopy 1975 Academic Press New York
    • (1975)
    • Vrieze, K1
  • 92
    • 85112937296 scopus 로고    scopus 로고
    • (c) Tobisch S. To be submitted for publication
  • 99
    • 85112885581 scopus 로고
    • (a) Mechanisms in Inorganic Chemistry 1973
    • (1973)
  • 101
    • 85112932548 scopus 로고
    • (c) M.L Tobe Comprehensive Coordination Chemistry 1973
    • (1973)
    • Tobe, M.L1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.