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1
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85112942897
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The oligomerization and co-oligomerization of butadiene and substituted 1,3-dienes
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(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
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(1975)
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Jolly, P.W1
Wilke, G2
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2
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85112876840
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Nickel-catalyzed oligomerization of 1,3-dienes related reactions
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(b) P.W Jolly Nickel-catalyzed oligomerization of 1,3-dienes related reactions Comprehensive Organometallic Chemistry Vol 8 1982
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(1982)
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Jolly, P.W1
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8
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85112947218
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Cyclooligomerizations and cyclo-co-oligomerizations of 1,3-dienes
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(c) G Wilke A ; Eckerle Cyclooligomerizations and cyclo-co-oligomerizations of 1,3-dienes Applied Homogeneous Catalysis with Organometallic Complexes 1996
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(1996)
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Wilke, G1
Eckerle, A3
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13
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85112888995
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(b) The catalytic cyclodimerization has been performed under the following reaction conditions: 80 °C, normal pressure, and nickel:ligand ratio 1:1
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14
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85112905207
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(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
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18
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85112898370
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(c) Kluth J. Ph.D. Thesis, University of Essen-Gesamthochschule, 1980
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20
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85112941684
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(b) The catalytic cyclotrimerization has been performed under the following conditions: 40–80 °C in liquid butadiene under pressure
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24
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85112891295
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(c) Tobisch S. Chem. Eur. J. 2003 , 9 , accepted
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32
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85112927237
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(d) Büssemeier B. Ph.D. Thesis, University of Bochum, 1973
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39
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85112872391
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P Heimbach R Traunmüller Chemie der Metall-Olefin-Komplexe, 1970 Verlag Chemie GmbH Weinheim
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(1970)
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Heimbach, P1
Traunmüller, R2
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42
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0001289535
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B Henc P.W Jolly R Salz G Wilke R Benn E.G Hoffmann R Mynott G Schroth K Seevogel J.C Sekutowski C Krüger J. Organomet. Chem. 191 1980 425
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(1980)
J. Organomet. Chem.
, vol.191
, pp. 425
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Henc, B1
Jolly, P.W2
Salz, R3
Wilke, G4
Benn, R5
Hoffmann, E.G6
Mynott, R7
Schroth, G8
Seevogel, K9
Sekutowski, J.C10
Krüger, C11
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43
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0000978596
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B Henc P.W Jolly R Salz S Stobbe G Wilke R Benn R Mynott K Seevogel R Goddard C Krüger J. Organomet. Chem. 191 1980 449
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(1980)
J. Organomet. Chem.
, vol.191
, pp. 449
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Henc, B1
Jolly, P.W2
Salz, R3
Stobbe, S4
Wilke, G5
Benn, R6
Mynott, R7
Seevogel, K8
Goddard, R9
Krüger, C10
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59
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85112879579
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12-cyclo-oligomer reaction channels can be found elsewhere ( Reference 11 )
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60
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85112943935
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(b) Detailed descriptions of the employed computational methodology are provided elsewhere ( Reference 11 )
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61
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85112917461
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3 ligands, the reader is referred to Reference 11b
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62
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85112875055
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For an overview see the recent special issue Computational Transition Metal Chemistry. Chem. Rev. 2000 , 100 , 351–818
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76
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85112917421
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(a) F Maseras Computational Organometallic Chemistry 2001
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(2001)
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Maseras, F1
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79
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85112906988
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(a) Full MM3(96) parameter set including π-systems
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88
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0002610072
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Fluxional allyl complexes
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(b) K Vrieze Fluxional allyl complexes Nuclear Magnetic Resonance Spectroscopy 1975 Academic Press New York
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(1975)
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Vrieze, K1
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92
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85112937296
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(c) Tobisch S. To be submitted for publication
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99
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85112885581
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(a) Mechanisms in Inorganic Chemistry 1973
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(1973)
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101
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85112932548
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(c) M.L Tobe Comprehensive Coordination Chemistry 1973
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(1973)
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Tobe, M.L1
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