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10
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0000269153
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-
(a)
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(a) S. Nakanishi, Y. Sawai, T. Yamamoto, T. Takata, Organometallics 15 (1996) 5432.
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(1996)
Organometallics
, vol.15
, pp. 5432
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Nakanishi, S.1
Sawai, Y.2
Yamamoto, T.3
Takata, T.4
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27
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85033876399
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note
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3); δ 7.02 (dd, J=15.3, 7.9 Hz, 1H), 5.93 (dd, J=15.3, 1.2 Hz, 1H), 4.73-4.65 (m, 1H), 4.22 (q, J=7.3 Hz, 2H), 1.83 (d, J=6.7 Hz, 3H), 1.30 (t, J=7.3 Hz, 3H).
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29
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85033878172
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3); δ 217.0, 216.8, 172.39, 97.3, 77.9, 60.9, 56.0, 19.6, 14.2
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3); δ 217.0, 216.8, 172.39, 97.3, 77.9, 60.9, 56.0, 19.6, 14.2.
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30
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85033903169
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1H-NMR sample. Thus signals (5.05 ppm) of the allylic protons were shifted to lower field (0.5 ppm) and were separated enough to determine the ratio of the enantiomers
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1H-NMR sample. Thus signals (5.05 ppm) of the allylic protons were shifted to lower field (0.5 ppm) and were separated enough to determine the ratio of the enantiomers.
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31
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0026782148
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For examples, Pd: (a)
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For examples, Pd: (a) I. Stary, J. Zajicek, P. Kocovsky, Tetrahedron, 48 (1992) 7229.
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(1992)
Tetrahedron
, vol.48
, pp. 7229
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Stary, I.1
Zajicek, J.2
Kocovsky, P.3
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32
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0001611087
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(b)
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(b) T. Hayashi, T. Hagihara, M. Konishi, M. Kumada, J. Am. Chem. Soc. 105 (1983) 7767.
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(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 7767
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Hayashi, T.1
Hagihara, T.2
Konishi, M.3
Kumada, M.4
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33
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0000596906
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Mo: (a)
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Mo: (a) Y.D. Ward, L.A. Villanueva, G.D. Allred, L.S. Liebeskind, J. Am. Chem. Soc. 118 (1996) 897.
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(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 897
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Ward, Y.D.1
Villanueva, L.A.2
Allred, G.D.3
Liebeskind, L.S.4
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38
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0003487210
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Mill Valley, CA: University Science
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Collman J.P., Hegedus L.S., Norton J.R., Finke R.G. Principles and Applications of Organo-transition Metal Chemistry. 1987;University Science, Mill Valley, CA.
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(1987)
Principles and Applications of Organo-transition Metal Chemistry
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Collman, J.P.1
Hegedus, L.S.2
Norton, J.R.3
Finke, R.G.4
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39
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85033896100
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1H-NMR (270 MHz, CDCl3) δ 7.80 (d, J=1.8 Hz, 2H), 7.33 (d, J=7.9 Hz, 2H), 6.67 (dd, J=15.9, 5.5 Hz, 1H), 5.87 (d, J=15.9, 1.8 Hz, 1H), 5.25-5.10 (m, 1H), 4.75-4.65 (m, 1H), 2.44 (s, 3H), 1.41 (d, J=6.7 Hz, 3H), 2.10-1.00 (m, 9H), 0.91 (d, J=6.7 Hz, 3H), 0.89 (d, J=7.3 Hz, 3H), 0.74 (d, J=7.3 Hz, 3H)
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1H-NMR (270 MHz, CDCl3) δ 7.80 (d, J=1.8 Hz, 2H), 7.33 (d, J=7.9 Hz, 2H), 6.67 (dd, J=15.9, 5.5 Hz, 1H), 5.87 (d, J=15.9, 1.8 Hz, 1H), 5.25-5.10 (m, 1H), 4.75-4.65 (m, 1H), 2.44 (s, 3H), 1.41 (d, J=6.7 Hz, 3H), 2.10-1.00 (m, 9H), 0.91 (d, J=6.7 Hz, 3H), 0.89 (d, J=7.3 Hz, 3H), 0.74 (d, J=7.3 Hz, 3H).
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-
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40
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85033878561
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3) δ 216.21, 215.91, 172.39, 96.80, 75.13, 61.16, 55.22, 47.03, 40.65, 34.26, 31.61, 26.30, 23.47, 22.07, 20.80, 16.37
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3) δ 216.21, 215.91, 172.39, 96.80, 75.13, 61.16, 55.22, 47.03, 40.65, 34.26, 31.61, 26.30, 23.47, 22.07, 20.80, 16.37.
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