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Martin, V. S.; Woodard, S. S.; Katsuki, T.; Yamada, Y.; Ikeda, M.; Sharpless, K. B. J. Am. Chem. Soc. 1981, 103, 6237.
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7
-
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0030984556
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For Noyori's highly enantioselective example of kinetic resolution with ArRuClTsdpen, see: (a) Hashiguchi, S.; Fujii, A.; Haack, K.-J.; Matsumura, K.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. Engl. 1997, 36, 288.
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Hashiguchi, S.1
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Matsumura, K.4
Ikariya, T.5
Noyori, R.6
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8
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0000898101
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For other selected kinetic resolution examples, see: (b) Nishibayashi, Y.; Takei, I.; Uemura, S.; Hidai, M. Organometallics 1999, 18, 2291.
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Nishibayashi, Y.1
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Hidai, M.4
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0033518869
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(c) Persson, B. A.; Larsson, A. L. E.; Le Ray, M.; Backvall, J.-E. J. Am. Chem. Soc. 1999, 121, 1645.
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Persson, B.A.1
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0001773245
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(d) Kitamura, M.; Ohkuma, T.; Tokunaga, M.; Noyori, R. Tetrahedron: Asymmetry 1990, 1, 1.
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Kitamura, M.1
Ohkuma, T.2
Tokunaga, M.3
Noyori, R.4
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12
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-
0033558168
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-
For selected examples of highly enantioselective and catalytic ketone hydrogenation, see: (a) Mikami, K.; Korenaga, T.; Terada, M.; Ohkuma, T.; Pham, T.; Noyori, R. Angew. Chem., Int Ed. 1999, 38, 495.
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Mikami, K.1
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Terada, M.3
Ohkuma, T.4
Pham, T.5
Noyori, R.6
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13
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0032479254
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(c) Doucet, H.; Ohkuma, T.; Murata, K.; Yokozawa, T.; Kozawa, M.; Katayama, E.; England, A. F.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. 1998, 37, 1703.
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Doucet, H.1
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Murata, K.3
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Kozawa, M.5
Katayama, E.6
England, A.F.7
Ikariya, T.8
Noyori, R.9
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14
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0032719707
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(e) Petra, D. G. I.; Kamer, P. C. J.; van Leeuwen, P. W. N. M.; Goubitz, K.; Van Loon, A. M.; de Vries, J. G.; Schoemaker, H. E. Eur. J. Inorg. Chem. 1999, 2335.
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Petra, D.G.I.1
Kamer, P.C.J.2
Van Leeuwen, P.W.N.M.3
Goubitz, K.4
Van Loon, A.M.5
De Vries, J.G.6
Schoemaker, H.E.7
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16
-
-
0043227817
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-
note
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2 and enantiopure cis-1-amino-2-indanol.
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-
-
-
17
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0042440143
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-
3, +0.54. McDaniel, D. H.; Brown, H. C., J. Org. Chem. 1958, 23, 420.
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(1958)
J. Org. Chem.
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McDaniel, D.H.1
Brown, H.C.2
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18
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0042225613
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-
See Supporting Information
-
See Supporting Information.
-
-
-
-
19
-
-
0041725298
-
-
note
-
Conversion = 15%, ee = 14% (R) at 3 days. Conversion = 25%, ee = 33% (A) at 20 days.
-
-
-
-
20
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0030984352
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(a) Haack, K.-J.; Hashiguchi, S.; Fujii, A.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. Engl. 1997, 36, 285.
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, pp. 285
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Haack, K.-J.1
Hashiguchi, S.2
Fujii, A.3
Ikariya, T.4
Noyori, R.5
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21
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0034614401
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(b) Kenny, J. A.; Versluis, K.; Heck, A. J. R.; Walsgrove, T.; Wills, M. Chem. Commun. 2000, 99-100.
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Kenny, J.A.1
Versluis, K.2
Heck, A.J.R.3
Walsgrove, T.4
Wills, M.5
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