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1
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0000172128
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Recent reviews: a, Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin
-
Recent reviews: a) T. Ohkuma, R. Noyori in Comprehensive Asymmetric Catalysis, Vol. 1 (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999, pp. 199-246;
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.1
, pp. 199-246
-
-
Ohkuma, T.1
Noyori, R.2
-
2
-
-
0003544583
-
-
2nd ed, Ed, I. Ojima, Wiley-VCH, New York
-
b) T. Ohkuma, M. Kitamura, R. Noyori in Catalytic Asymmetric Synthesis, 2nd ed. (Ed.: I. Ojima), Wiley-VCH, New York, 2000, pp. 1-110;
-
(2000)
Catalytic Asymmetric Synthesis
, pp. 1-110
-
-
Ohkuma, T.1
Kitamura, M.2
Noyori, R.3
-
3
-
-
33947121464
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-
2nd ed, Eds, M. Beller, C. Bolm, Wiley-VCH, Weinheim
-
c) T. Ohkuma, R. Noyori in Transition Metals for Organic Synthesis, Vol. 2, 2nd ed. (Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim, 2004, pp. 29-113;
-
(2004)
Transition Metals for Organic Synthesis
, vol.2
, pp. 29-113
-
-
Ohkuma, T.1
Noyori, R.2
-
4
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84891035198
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Eds, J. G. de Vries, C. J. Elsevier, Wiley-VCH, Weinheim
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d) T. Ohkuma, R. Noyori in The Handbook of Homogeneous Hydrogenation, Vol. 3 (Eds.: J. G. de Vries, C. J. Elsevier), Wiley-VCH, Weinheim, 2007, pp. 1105-1163.
-
(2007)
The Handbook of Homogeneous Hydrogenation
, vol.3
, pp. 1105-1163
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Ohkuma, T.1
Noyori, R.2
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5
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54749144045
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Xyl-binap=2,2′-bis(di-3,5-xylylphosphanyl)-1,1′-binaphthyl. Daipen=1,1-di(4-anisyl)-2-isopropyl-1,2-ethylenediamine. Tolbinap= 2,2′-bis(di-4-tolylphosphanyl)-1,1′-binaphthyl. Dmapen=2- dimethylamino-1-phenylethylamine. Dpen=1,2-diphenylethylenediamine.
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Xyl-binap=2,2′-bis(di-3,5-xylylphosphanyl)-1,1′-binaphthyl. Daipen=1,1-di(4-anisyl)-2-isopropyl-1,2-ethylenediamine. Tolbinap= 2,2′-bis(di-4-tolylphosphanyl)-1,1′-binaphthyl. Dmapen=2- dimethylamino-1-phenylethylamine. Dpen=1,2-diphenylethylenediamine.
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6
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0032583505
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T. Ohkuma, M. Koizumi, H. Doucet, T. Pham, M. Kozawa, K. Murata, E. Katayama, T. Yokozawa, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1998, 120, 13529-13530.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 13529-13530
-
-
Ohkuma, T.1
Koizumi, M.2
Doucet, H.3
Pham, T.4
Kozawa, M.5
Murata, K.6
Katayama, E.7
Yokozawa, T.8
Ikariya, T.9
Noyori, R.10
-
9
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20444437938
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a) T. Ohkuma, C. A. Sandoval, R. Srinivasan, Q. Lin, Y. Wei, K. Muñiz, R. Noyori, J. Am. Chem. Soc. 2005, 127, 8288-8289.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 8288-8289
-
-
Ohkuma, T.1
Sandoval, C.A.2
Srinivasan, R.3
Lin, Q.4
Wei, Y.5
Muñiz, K.6
Noyori, R.7
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10
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54749088784
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For hydrogenation of acyl silanes, see:b
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For hydrogenation of acyl silanes, see:b) N. Arai, K. Suzuki, S. Sugizaki, H. Sorimachi, T. Ohkuma, Angew. Chem. 2008, 120, 1794-1797;
-
(2008)
Angew. Chem
, vol.120
, pp. 1794-1797
-
-
Arai, N.1
Suzuki, K.2
Sugizaki, S.3
Sorimachi, H.4
Ohkuma, T.5
-
11
-
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53549133355
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-
Angew. Chem. Int. Ed. 2008, 47, 1770-1773.
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 1770-1773
-
-
-
12
-
-
0001286347
-
-
T. Ohkuma, M. Koizumi, H. Ikehira, T. Yokozawa, R. Noyori, Org. Lett. 2000, 2, 659-662.
-
(2000)
Org. Lett
, vol.2
, pp. 659-662
-
-
Ohkuma, T.1
Koizumi, M.2
Ikehira, H.3
Yokozawa, T.4
Noyori, R.5
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13
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0000471847
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Hydrogenation of 1a with a chiral iridium catalyst gave the allylic alcohol in 9% ee and 56% yield. See: C. Bianchini, E. Farnetti, L. Glendenning, M. Graziani, G. Nargin, M. Peruzzini, E. Rocchini, F. Zanobini, Organometallics 1995, 14, 1489-1502.
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Hydrogenation of 1a with a chiral iridium catalyst gave the allylic alcohol in 9% ee and 56% yield. See: C. Bianchini, E. Farnetti, L. Glendenning, M. Graziani, G. Nargin, M. Peruzzini, E. Rocchini, F. Zanobini, Organometallics 1995, 14, 1489-1502.
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16
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34547492829
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See also: c
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See also: c) N. Kawai, S. M. Hande, J. Uenishi, Tetrahedron 2007, 63, 9049-9056.
-
(2007)
Tetrahedron
, vol.63
, pp. 9049-9056
-
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Kawai, N.1
Hande, S.M.2
Uenishi, J.3
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17
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0001015795
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For asymmetric borane reduction catalyzed by chiral oxazaborolidines, see
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For asymmetric borane reduction catalyzed by chiral oxazaborolidines, see: E. J. Corey, C. J. Helal, Angew. Chem. 1998, 110, 2092-2118;
-
(1998)
Angew. Chem
, vol.110
, pp. 2092-2118
-
-
Corey, E.J.1
Helal, C.J.2
-
18
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0032541271
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-
Angew. Chem. Int. Ed. 1998, 37, 1986-2012.
-
(1998)
Angew. Chem. Int. Ed
, vol.37
, pp. 1986-2012
-
-
-
19
-
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54749083103
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-
S. Woodward, A. Ford (The University of Hull), UK-GB 2339780A, 1998.
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S. Woodward, A. Ford (The University of Hull), UK-GB 2339780A, 1998.
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21
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II complex. See: N. Arai, H. Ooka, K. Azuma, T. Yabuuchi, N. Kurono, T. Inoue, T. Ohkuma, Org. Lett. 2007, 9, 939-941.
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II complex. See: N. Arai, H. Ooka, K. Azuma, T. Yabuuchi, N. Kurono, T. Inoue, T. Ohkuma, Org. Lett. 2007, 9, 939-941.
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22
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0346836894
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Conjugate reduction of 1a by hydrogenation or transfer hydrogenation with metal complexes. See: a L. Dahlenburg, K. Herbst, A. Zahl, J. Organomet. Chem. 2000, 616, 19-28;
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Conjugate reduction of 1a by hydrogenation or transfer hydrogenation with metal complexes. See: a) L. Dahlenburg, K. Herbst, A. Zahl, J. Organomet. Chem. 2000, 616, 19-28;
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-
-
23
-
-
0036169287
-
-
b) J. Hannedouche, J. A. Kenny, T. Walsgrove, M. Wills, Synlett 2002, 263-266;
-
(2002)
Synlett
, pp. 263-266
-
-
Hannedouche, J.1
Kenny, J.A.2
Walsgrove, T.3
Wills, M.4
-
24
-
-
17744381791
-
-
D. Xue, Y.-C. Chen, X. Cui, Q.-W. Wang, J. Zhu, J.-G. Deng, J. Org. Chem. 2005, 70, 3584-3591. See also reference [7].
-
c) D. Xue, Y.-C. Chen, X. Cui, Q.-W. Wang, J. Zhu, J.-G. Deng, J. Org. Chem. 2005, 70, 3584-3591. See also reference [7].
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25
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Isolated 2h was readily decomposed at ambient temperature.
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Isolated 2h was readily decomposed at ambient temperature.
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26
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0242270864
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C. A. Sandoval, T. Ohkuma, K. Muñiz, R. Noyori, J. Am. Chem. Soc. 2003, 125, 13490-13503.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 13490-13503
-
-
Sandoval, C.A.1
Ohkuma, T.2
Muñiz, K.3
Noyori, R.4
-
27
-
-
0037132617
-
-
a) K. Abdur-Rashid, S. E. Clapham, A. Hadzovic, J. N. Harvey, A. J. Lough, R. H. Morris, J. Am. Chem. Soc. 2002, 124, 15104-15118;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 15104-15118
-
-
Abdur-Rashid, K.1
Clapham, S.E.2
Hadzovic, A.3
Harvey, J.N.4
Lough, A.J.5
Morris, R.H.6
-
29
-
-
34250025202
-
-
c) S. A. French, D. Di Tommaso, A. Zanotti-Gerosa, F. Hancock, C. R. A. Catlow, Chem. Commun. 2007, 2381-2388.
-
(2007)
Chem. Commun
, pp. 2381-2388
-
-
French, S.A.1
Di Tommaso, D.2
Zanotti-Gerosa, A.3
Hancock, F.4
Catlow, C.R.A.5
-
30
-
-
0000124143
-
-
a) F. Maseras, A. Lledós, E. Clot, O. Eisenstein, Chem. Rev. 2000, 100, 601-636;
-
(2000)
Chem. Rev
, vol.100
, pp. 601-636
-
-
Maseras, F.1
Lledós, A.2
Clot, E.3
Eisenstein, O.4
-
32
-
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Repulsive interaction between the filled p and d orbitals has also been postulated: K. G. Caulton, New J. Chem. 1994, 18, 25-41.
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Repulsive interaction between the filled p and d orbitals has also been postulated: K. G. Caulton, New J. Chem. 1994, 18, 25-41.
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33
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Si.
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Si.
-
-
-
-
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-
-
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-
-
H.-F. Duan, J.-H. Xie, W.-J. Shi, Q. Zhang, Q.-L. Zhou, Org. Lett. 2006, 8, 1479-1481.
-
(2006)
Org. Lett
, vol.8
, pp. 1479-1481
-
-
Duan, H.-F.1
Xie, J.-H.2
Shi, W.-J.3
Zhang, Q.4
Zhou, Q.-L.5
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