-
1
-
-
29144521717
-
-
For recent reviews, see
-
For recent reviews, see:, Glorius F, Org. Biomol. Chem. 2005 3 4171
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 4171
-
-
Glorius, F.1
-
4
-
-
0041825591
-
-
Wang W.-B, Lu S.-M, Yang P.-Y, Han X.-W, Zhou Y.-G, J. Am. Chem. Soc. 2003 125 10536
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 10536
-
-
Wang, W.-B.1
Lu, S.-M.2
Yang, P.-Y.3
Han, X.-W.4
Zhou, Y.-G.5
-
5
-
-
4444307960
-
-
For selected recent examples of asymmetric hydrogenation of quinolines, see
-
For selected recent examples of asymmetric hydrogenation of quinolines, see:, Lu S.-M, Han X.-W, Zhou Y.-G, Adv. Synth. Catal. 2004 346 909
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 909
-
-
Lu, S.-M.1
Han, X.-W.2
Zhou, Y.-G.3
-
6
-
-
64549090253
-
-
Wang D.-W, Wang X.-B, Wang D.-S, Lu S.-M, Zhou Y.-G, Li Y.-X, J. Org. Chem. 2009 74 2780
-
(2009)
J. Org. Chem.
, vol.74
, pp. 2780
-
-
Wang, D.-W.1
Wang, X.-B.2
Wang, D.-S.3
Lu, S.-M.4
Zhou, Y.-G.5
Li, Y.-X.6
-
8
-
-
16644386624
-
-
Xu L.-J, Lam K H., Ji J X., Fan Q.-H, Lo W.-H, Chan A S. C., Chem. Commun. 2005 1390
-
(2005)
Chem. Commun.
, pp. 1390
-
-
Xu, L.-J.1
Lam, K.H.2
Ji, J.X.3
Fan, Q.-H.4
Lo, W.-H.5
Chan, A.S.C.6
-
9
-
-
33846816454
-
-
Tang W.-J, Zhu S.-F, Xu L.-J, Zhou Q.-L, Fan Q.-H, Zhou H.-F, Lam K, Chan A S. C., Chem. Commun. 2007 613
-
(2007)
Chem. Commun.
, pp. 613
-
-
Tang, W.-J.1
Zhu, S.-F.2
Xu, L.-J.3
Zhou, Q.-L.4
Fan, Q.-H.5
Zhou, H.-F.6
Lam, K.7
Chan, A.S.C.8
-
10
-
-
34147102783
-
-
Wang Z J., Deng G J., Li Y, He Y M., Tang W J., Fan Q H., Org. Lett. 2007 9 1243
-
(2007)
Org. Lett.
, vol.9
, pp. 1243
-
-
Wang, Z.J.1
Deng, G.J.2
Li, Y.3
He, Y.M.4
Tang, W.J.5
Fan, Q.H.6
-
12
-
-
53949112678
-
-
Mri N, Lefort L, Boogers J A. F., Minnaard A J., Feringa B L., de Vries J G., Adv. Synth. Catal. 2008 350 1081
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1081
-
-
Mri, N.1
Lefort, L.2
Boogers, J.A.F.3
Minnaard, A.J.4
Feringa, B.L.5
De Vries, J.G.6
-
13
-
-
70349653339
-
-
Tadaoka H, Cartigny D, Nagano T, Gosavi T, Ayad T, Genêt J P., Ohshima T, Ratovelomanana-Vidal V, Mashima K, Chem. Eur. J. 2009 15 9990
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 9990
-
-
Tadaoka, H.1
Cartigny, D.2
Nagano, T.3
Gosavi, T.4
Ayad, T.5
Genêt, J.P.6
Ohshima, T.7
Ratovelomanana-Vidal, V.8
Mashima, K.9
-
14
-
-
54249139518
-
-
Zhou H F., Li Z W., Wang Z J., Wang T L., Xu L J., He Y M., Fan Q.-H, Pan J, Gu L Q., Chan A S. C., Angew. Chem. Int. Ed. 2008 47 8464
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 8464
-
-
Zhou, H.F.1
Li, Z.W.2
Wang, Z.J.3
Wang, T.L.4
Xu, L.J.5
He, Y.M.6
Fan, Q.-H.7
Pan, J.8
Gu, L.Q.9
Chan, A.S.C.10
-
15
-
-
67649132809
-
-
Wang Z.-J, Zhou H.-F, Wang T.-L, He Y.-M, Fan Q.-H, Green Chem. 2009 11 767
-
(2009)
Green Chem.
, vol.11
, pp. 767
-
-
Wang, Z.-J.1
Zhou, H.-F.2
Wang, T.-L.3
He, Y.-M.4
Fan, Q.-H.5
-
16
-
-
58149202442
-
-
Li Z.-W, Wang T.-L, He Y.-M, Wang Z.-J, Fan Q.-H, Pan J, Xu L.-J, Org. Lett. 2008 10 5265
-
(2008)
Org. Lett.
, vol.10
, pp. 5265
-
-
Li, Z.-W.1
Wang, T.-L.2
He, Y.-M.3
Wang, Z.-J.4
Fan, Q.-H.5
Pan, J.6
Xu, L.-J.7
-
17
-
-
79954608119
-
-
For selected examples of asymmetric hydrogenation of other heteroaromatic compounds, see: For indoles and pyrroles
-
For selected examples of asymmetric hydrogenation of other heteroaromatic compounds, see: For indoles and pyrroles
-
-
-
-
18
-
-
0034625892
-
-
Kuwano R, Sato K, Kurokawa T, Karube D, Ito Y, J. Am. Chem. Soc. 2000 122 7614
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 7614
-
-
Kuwano, R.1
Sato, K.2
Kurokawa, T.3
Karube, D.4
Ito, Y.5
-
19
-
-
77954262931
-
-
Wang D.-S, Chen Q.-A, Li W, Yu C.-B, Zhou Y.-G, Zhang X, J. Am. Chem. Soc. 2010 132 8909
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 8909
-
-
Wang, D.-S.1
Chen, Q.-A.2
Li, W.3
Yu, C.-B.4
Zhou, Y.-G.5
Zhang, X.6
-
20
-
-
38349135761
-
-
Kuwano R, Kashiwabara M, Ohsumi M, Kusano H, J. Am. Chem. Soc. 2008 130 808
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 808
-
-
Kuwano, R.1
Kashiwabara, M.2
Ohsumi, M.3
Kusano, H.4
-
21
-
-
33747233073
-
-
For furans, see
-
For furans, see:, Kaiser S, Smidt S P., Pfaltz A, Angew. Chem. Int. Ed. 2006 45 5194
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 5194
-
-
Kaiser, S.1
Smidt, S.P.2
Pfaltz, A.3
-
23
-
-
33745576403
-
-
For isoquinolines, see
-
For isoquinolines, see:, Lu S M., Wang Y Q., Han X W., Zhou Y.-G, Angew. Chem. Int. Ed. 2006 45 2260
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 2260
-
-
Lu, S.M.1
Wang, Y.Q.2
Han, X.W.3
Zhou, Y.-G.4
-
24
-
-
70449591239
-
-
Tang W.-J, Xu L.-J, Fan Q.-H, Wang J, Fan B.-M, Lam K.-H, Chan A S. C., Angew. Chem. Int. Ed. 2009 48 9135
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 9135
-
-
Tang, W.-J.1
Xu, L.-J.2
Fan, Q.-H.3
Wang, J.4
Fan, B.-M.5
Lam, K.-H.6
Chan, A.S.C.7
-
25
-
-
70549106501
-
-
Mri N, Jerphagnon T, Minnaard A J., Feringa B L., de Vries J G., Adv. Synth. Catal. 2009 351 2549
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 2549
-
-
Mri, N.1
Jerphagnon, T.2
Minnaard, A.J.3
Feringa, B.L.4
De Vries, J.G.5
-
26
-
-
37049097270
-
-
Carey A R. E., Fukata G, O'Ferrall R A. M., Murphy M G., J. Chem. Soc., Perkin Trans. 2 1985 1711
-
(1985)
J. Chem. Soc., Perkin Trans. 2
, pp. 1711
-
-
Carey, A.R.E.1
Fukata, G.2
O'Ferrall, R.A.M.3
Murphy, M.G.4
-
27
-
-
0035809278
-
-
For metal complexes containing diamine ligands for asymmetric hydrogenation, see
-
For metal complexes containing diamine ligands for asymmetric hydrogenation, see:, Ito M, Hirakawa M, Murata K, Ikariya T, Organometallics 2001 20 379
-
(2001)
Organometallics
, vol.20
, pp. 379
-
-
Ito, M.1
Hirakawa, M.2
Murata, K.3
Ikariya, T.4
-
28
-
-
33745933460
-
-
Ohkuma T, Utsumi N, Tsutsumi K, Murata K, Sandoval C A., Noyori R, J. Am. Chem. Soc. 2006 128 8724
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 8724
-
-
Ohkuma, T.1
Utsumi, N.2
Tsutsumi, K.3
Murata, K.4
Sandoval, C.A.5
Noyori, R.6
-
29
-
-
33846628216
-
-
Ohkuma T, Tsutsumi K, Utsumi N, Arai N, Noyori R, Murata K, Org. Lett. 2007 9 255
-
(2007)
Org. Lett.
, vol.9
, pp. 255
-
-
Ohkuma, T.1
Tsutsumi, K.2
Utsumi, N.3
Arai, N.4
Noyori, R.5
Murata, K.6
-
31
-
-
78751606820
-
-
Chen f, Wang T.-L, He Y.-M, Ding Z.-Y, Li Z.-W, Xu L.-J, Fan Q.-H, Chem. Eur. J. 2011 17 1109
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 1109
-
-
Chen, F.1
Wang, T.-L.2
He, Y.-M.3
Ding, Z.-Y.4
Li, Z.-W.5
Xu, L.-J.6
Fan, Q.-H.7
-
32
-
-
65549144060
-
-
Wang X.-B, Wang D.-W, Lu S.-M, Yu C.-B, Zhou Y.-G, Tetrahedron: Asymmetry 2009 20 1040
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1040
-
-
Wang, X.-B.1
Wang, D.-W.2
Lu, S.-M.3
Yu, C.-B.4
Zhou, Y.-G.5
-
34
-
-
0001040853
-
-
Hashiguchi S, Fujii A, Takehara J, Ikariya T, Noyori R, J. Am. Chem. Soc. 1995 117 7562
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 7562
-
-
Hashiguchi, S.1
Fujii, A.2
Takehara, J.3
Ikariya, T.4
Noyori, R.5
-
35
-
-
0031035167
-
-
Sidler D R., Sager J W., Bergan J J., Wells K M., Bhupathy M, Volante R P., Tetrahedron: Asymmetry 1997 8 161
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 161
-
-
Sidler, D.R.1
Sager, J.W.2
Bergan, J.J.3
Wells, K.M.4
Bhupathy, M.5
Volante, R.P.6
-
36
-
-
70349902205
-
-
For transition-metal-catalyzed asymmetric transfer hydrogenation of quinolines in acidic aqueous buffer solution, see
-
For transition-metal-catalyzed asymmetric transfer hydrogenation of quinolines in acidic aqueous buffer solution, see:, Wang C, Li C, Wu X, Pettman A, Xiao J, Angew. Chem. Int. Ed. 2009 48 6524
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 6524
-
-
Wang, C.1
Li, C.2
Wu, X.3
Pettman, A.4
Xiao, J.5
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