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Hashiguchi, S.; Fujii, A.; Takehara, J.; Ikariya, T.; Noyori, R. J. Am. Chem. Soc. 1995, 117, 7562-7563.
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Hashiguchi, S.1
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2
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5844367837
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J. Chem. Soc., Chem. Commun., in Press
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Takehara, J.1
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Noyori, R.6
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3
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0001767033
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Evans, D.A.1
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6
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Zassinovich, G.1
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Gamez, P.1
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8
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37049067470
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Gamez, P.1
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De Graauw, C.F.1
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12
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0001736711
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(a) Wong, W.-K.; Gao, J.-X.; Zhou, Z.-Y.; Mak, T. C. W. Polyhedron 1993, 12, 1415-1417.
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Wong, W.-K.1
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13
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33847085550
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14
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0007751865
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(c) Wong, W.-K.; Lai, K.-K.; Tse, M.-S.; Tse, M.-C.; Gao, J.-X.; Wong, W.-T.; Chan, S. Polyhedron 1994, 13, 2751-2762.
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Wong, W.-K.1
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Tse, M.-C.4
Gao, J.-X.5
Wong, W.-T.6
Chan, S.7
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15
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5844416241
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note
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2Ru (833.91): C, 63.32; H, 5.28; N, 3.36. Found: C, 63.07; H, 5.45; N, 3.30.
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16
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5844381076
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note
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Actual crystallographic analysis was done for (R,R)-4 (Supporting Information). For convenience in the structural comparison, the geometry of the S,S isomer is given.
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17
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5844359796
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note
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w) = 0.033 (0.027) for 3419 observed reflections (I > 3.00σ-(I)).
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18
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5844400579
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note
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5
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19
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5844412449
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note
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The (S,S)-4-catalyzed reaction of 5a in a 1 M 2-propanol solution at 23 °C gave (R)-6a in 95% ee and in 87% yield after 24 h and in 95% ee and 93% yield after 44 h. The reaction of the p-chloro compound p-5b (0.1 M, 45 °C) afforded (R)-p-6b in 94% ee and in 95% yield after 5 h, and these values did not change even after 29 h.
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21
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0002680730
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(b) Gao, Y.-C.; Shi, Q.-Z.; Kershner, D. L.; Basolo, F. Inorg. Chem. 1988, 27, 188-191.
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(1988)
Inorg. Chem.
, vol.27
, pp. 188-191
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Gao, Y.-C.1
Shi, Q.-Z.2
Kershner, D.L.3
Basolo, F.4
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