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0001847287
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Tail-to-head: (a) Yagi, H.; Tanaka, E.; Ishiwatari, H.; Hidai, M.; Uchida, Y. Synthesis 1977, 9, 334-335.
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Yagi, H.1
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0002646787
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0002180731
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Tail-to-tail
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Dani, P.1
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0011650659
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0020805025
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(a) Keim, W.; Behr, A.; Rzehak, H. Tenside Deterg. 1979, 26, 113-116.
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0009235286
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(d) Petrushkina, E. A.; Gavrilenko, V. V.; Oprunenko, Y. F.; Akhmedov, N. G. Zh. Obshch. Khim. 1996, 66, 1864-1870.
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Petrushkina, E.A.1
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23
-
-
0343924072
-
-
See Experimental Section for details
-
See Experimental Section for details.
-
-
-
-
24
-
-
0343924073
-
-
3c,d
-
3c,d.
-
-
-
-
25
-
-
37049132741
-
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(a) Atkins, K. E.; Walker, W. E.; Manyik, R. M. J. Chem. Soc., Chem. Commun. 1971, 330.
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26
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0001551154
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(b) Kaneda, H.; Kurosaki, H.; Terasawa, M.; Imanaka, T.; Teranishi, S. J. Org. Chem. 1981, 46, 2356-2362.
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Teranishi, S.5
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27
-
-
8944246772
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(c) Bianchini, J. P.; Waegell, B.; Gaydou, E. M.; Rzehak, H.; Keim, W. J. Mol. Catal. 1981, 10, 247-252.
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Bianchini, J.P.1
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28
-
-
0022113838
-
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Röper, M.; He, R.; Schieren, M. J. Mol. Catal. 1985, 31, 335-343.
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Röper, M.1
He, R.2
Schieren, M.3
-
29
-
-
0343052412
-
-
In this case, as in all others examined, raising the temperature to 60 °C gave increasing amounts of other unidentified products, without substantial change in selectivity of the telomerization reaction
-
In this case, as in all others examined, raising the temperature to 60 °C gave increasing amounts of other unidentified products, without substantial change in selectivity of the telomerization reaction.
-
-
-
-
30
-
-
0033570981
-
-
Note that interesting tail-to-tail selectivity has been achieved in a multicomponent diene coupling process
-
Note that interesting tail-to-tail selectivity has been achieved in a multicomponent diene coupling process: Kimura, M.; Matsuo, S.; Shibata, K.; Tamara, Y. Angew. Chem., Int. Ed. 1999, 38, 3386-3388.
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(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 3386-3388
-
-
Kimura, M.1
Matsuo, S.2
Shibata, K.3
Tamara, Y.4
-
33
-
-
0342618169
-
-
The ligand is now commercially available
-
(c) The ligand is now commercially available.
-
-
-
-
34
-
-
0342618165
-
-
3 system is not completely homogeneous, requiring the use of the soluble cationic allylpalladium starting material for kinetics
-
3 system is not completely homogeneous, requiring the use of the soluble cationic allylpalladium starting material for kinetics.
-
-
-
-
35
-
-
0343924069
-
-
note
-
1H NMR spectroscopy. Graphs of the amount of isoprene remaining vs time provided straight lines through more than 50% completion, consistent with zero-order (saturated) kinetics, and the rates were calculated from the measured slopes of these lines.
-
-
-
-
36
-
-
0000709185
-
-
and references therein
-
(a) Benn, R.; Jolly, P. W.; Mynott, R.; Schenker, G.; Schick, K.-P.; Schroth, G. Organometallics 1985, 4, 1945-1953 and references therein.
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Schenker, G.4
Schick, K.-P.5
Schroth, G.6
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37
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(b) Jolly, P. W.; Mynott, R.; Raspel, B.; Schick, K.-P. Organometallics 1986, 5, 473-481.
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38
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Bianchini, J.P.1
Gaydou, E.M.2
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Keim, W.5
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43
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0002598511
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46
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Tani, K.1
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