Indexed keywords
ASYMMETRIC HYDROGENATION;
BISPHOSPHINE;
ELECTRON WITHDRAWING GROUP;
ELECTRON-DEFICIENT;
IRIDIUM COMPLEX;
QUINOLINES;
TURNOVER NUMBER;
CATALYST ACTIVITY;
CHELATION;
ENANTIOSELECTIVITY;
HYDROGENATION;
IRIDIUM;
IRIDIUM COMPOUNDS;
LIGANDS;
1,2,3,4 TETRAHYDRO 2 METHYLQUINOLINE;
2 (3' BENZYLOXY 4' METHOXYPHENETHYL) 1,2,3,4 TETRAHYDROQUINOLINE;
2 (3',4' DIMETHOXYPHENETHYL) 1,2,3,4 TETRAHYDROQUINOLINE;
2 BUTYL 1,2,3,4 TETRAHYDROQUINOLINE;
2 ETHYL 1,2,3,4 TETRAHYDROQUINOLINE;
2 METHYL 1 (1,2,3,4 TETRAHYDROQUINOLIN 2 YL)PROPAN 2 OL;
2 PENTYL 1,2,3,4 TETRAHYDROQUINOLINE;
2 PHENYL 1,2,3,4 TETRAHYDROQUINOLINE;
2 PROPYL 1,2,3,4 TETRAHYDROQUINOLINE;
2,6 DIMETHYL 1,2,3,4 TETRAHYDROQUINOLINE;
6 FLUORO 2 METHYL 1,2,3,4 TETRAHYDROQUINOLINE;
6,6' BIS(DIPHENYLPHOSPHINO) 1,1' BIPHENYL 2,2' DIYLBIS(2,3,4,5,6 PENTAFLUOROBENZENECARBOXYLATE);
6,6' BIS(DIPHENYLPHOSPHINO) 1,1' BIPHENYL 2,2' DIYLBIS(3,5 BISTRIFLUOROMETHYLBENZENECARBOXYLATE);
6,6' BIS(DIPHENYLPHOSPHINO) 1,1' BIPHENYL 2,2' DIYLBIS(4 METHOXYBENZENECARBOXYLATE);
6,6' BIS(DIPHENYLPHOSPHINO) 1,1' BIPHENYL 2,2' DIYLBIS(BENZENECARBOXYLATE);
6,6' BIS(DIPHENYLPHOSPHINO) 1,1' BIPHENYL 2,2' DIYLBIS(CYCOHEXANECARBOXYLATE);
6,6' BIS(DIPHENYLPHOSPHINO) 1,1' BIPHENYL 2,2' DIYLBIS(TRIFLUOROMETHYLSULFONATE);
BIPHOSPHINE DERIVATIVE;
PHOSPHINE DERIVATIVE;
QUINOLONE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CATALYST;
CHEMICAL REACTION;
COMPLEX FORMATION;
DRUG SYNTHESIS;
ENANTIOSELECTIVITY;
HYDROGENATION;
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
0142131269
For recent reviews on hydrogenation of heteroaromatic compounds, see:, Dyson P J., Dalton Trans. 2003 2964
(2003)
Dalton Trans.
, pp. 2964
Dyson, P.J.1
10
4444307960
For our groups work on the 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
13
33745576403
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
16
64549090253
[nl]
Wang D.-W, Wang X.-B, Wang D.-S, Lu [nl]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
17
76549121080
Wang D.-W, Wang D.-S, Chen Q.-A, Zhou Y.-G, Chem. Eur. J. 2010 16 1133
(2010)
Chem. Eur. J.
, vol.16
, pp. 1133
Wang, D.-W.1
Wang, D.-S.2
Chen, Q.-A.3
Zhou, Y.-G.4
19
10844284455
For other groups work on metal-catalyzed asymmetric hydrogenation of quinolines, see:, Fache F, Synlett 2004 2827
(2004)
Synlett
, pp. 2827
Fache, F.1
20
1642603931
Fujita K.-I, Kitatsuji C, Furukawa S, Yamaguchi R, Tetrahedron Lett. 2004 45 3215
(2004)
Tetrahedron Lett.
, vol.45
, pp. 3215
Fujita, K.-I.1
Kitatsuji, C.2
Furukawa, S.3
Yamaguchi, R.4
21
16644386624
Xu L.-J, Lam K.-H, Ji J.-X, Wu J, 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
Wu, J.4
Fan, Q.-H.5
Lo, W.-H.6
Chan, A.S.C.7
22
28244476491
[nl]
Lam [nl]K.-H, Xu L.-J, Feng L.-C, Fan Q.-H, Lam F.-L, Lo W.-H, Chan A S. C., Adv. Synth. Catal. 2005 347 1755
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1755
Lam, K.-H.1
Xu, L.-J.2
Feng, L.-C.3
Fan, Q.-H.4
Lam, F.-L.5
Lo, W.-H.6
Chan, A.S.C.7
25
33646677236
Qiu L, Kwong F Y., Wu J, Lam W H., Chan S, Yu W.-Y, Li Y.-M, Guo R, Zhou Z, Chan A S. C., J. Am. Chem. Soc. 2006 128 5955
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5955
Qiu, L.1
Kwong, F.Y.2
Wu, J.3
Lam, W.H.4
Chan, S.5
Yu, W.-Y.6
Li, Y.-M.7
Guo, R.8
Zhou, Z.9
Chan, A.S.C.10
26
33744501305
Yamagata T, Tadaoka H, Nagata M, Hirao T, Kataoka Y, Ratovelomanana-Vidal V, Genet J P., Mashima K, Organometallics 2006 25 2505
(2006)
Organometallics
, vol.25
, pp. 2505
Yamagata, T.1
Tadaoka, H.2
Nagata, M.3
Hirao, T.4
Kataoka, Y.5
Ratovelomanana-Vidal, V.6
Genet, J.P.7
Mashima, K.8
27
36448942937
Chan S.-H, Lam K.-H, Li Y.-M, Xu L.-J, Tang W.-J, Lam F.-L, Lo W.-H, Yu W.-Y, Fan Q.-H, Chan A S. C., Tetrahedron: Asymmetry 2007 18 2625
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2625
Chan, S.-H.1
Lam, K.-H.2
Li, Y.-M.3
Xu, L.-J.4
Tang, W.-J.5
Lam, F.-L.6
Lo, W.-H.7
Yu, W.-Y.8
Fan, Q.-H.9
Chan, A.S.C.10
28
35649004432
Deport C, Buchotte M, Abecassis K, Tadaoka H, Ayad T, Ohshima T, Genet J.-P, Mashima K, Ratovelomanana-Vidal V, Synlett 2007 2743
(2007)
Synlett
, pp. 2743
Deport, C.1
Buchotte, M.2
Abecassis, K.3
Tadaoka, H.4
Ayad, T.5
Ohshima, T.6
Genet, J.-P.7
Mashima, K.8
Ratovelomanana-Vidal, V.9
29
58149202442
[nl]
Li [nl]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
30
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
32
53949112678
Mri N, Lefort L, Boogers J A. F., Minnaard A J., Feringa B L., deVries 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
Devries, J.G.6
33
63349093184
Eggenstein M, Thomas A, Theuerkauf J, Franci G, Leitner W, Adv. Synth. Catal. 2009 351 725
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 725
Eggenstein, M.1
Thomas, A.2
Theuerkauf, J.3
Franci, G.4
Leitner, W.5
34
70349902205
Wang C, Li C.-Q, Wu X.-F, Pettman A, Xiao J.-L, Angew. Chem. Int. Ed. 2009 48 6524
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 6524
Wang, C.1
Li, C.-Q.2
Wu, X.-F.3
Pettman, A.4
Xiao, J.-L.5
35
70349653339
Tadaoka H, Cartigny D, Nagano T, Gosavi T, Ayad T, Genet 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
Genet, J.-P.6
Ohshima, T.7
Ratovelomanana-Vidal, V.8
Mashima, K.9
36
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
38
78349289940
Gou F.-R, Li W, Zhang X M., Liang Y.-M, Adv. Synth. Catal. 2010 352 2441
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 2441
Gou, F.-R.1
Li, W.2
Zhang, X.M.3
Liang, Y.-M.4
39
33746269442
For the work on organocatalytic asymmetric hydrogenation of quinolines, see:, Rueping M, Antonchick A P., Theissmann T, Angew. Chem. Int. Ed. 2006 45 3683
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 3683
Rueping, M.1
Antonchick, A.P.2
Theissmann, T.3
40
53249093355
Rueping M, Theissmann T, Raja S, Bats J W. P., Adv. Synth. Catal. 2008 350 1001
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 1001
Rueping, M.1
Theissmann, T.2
Raja, S.3
Bats, J.W.P.4
43
70549106501
Mri N, Jerphagnon T, Minnaard A J., Feringa B L., deVries 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
Devries, J.G.5
44
70449591239
Tang W.-J, Xu L.-J, Fan Q.-H, Wang J, Fan B.-M, Zhou Z.-Y, 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
Zhou, Z.-Y.6
Lam, K.-H.7
Chan, A.S.C.8
45
77956376839
Cartigny D, Nagano T, Ayad T, Genet J P., Ohshima T, Mashima K, Ratovelomanana-Vidal V, Adv. Synth. Catal. 2010 352 1886
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1886
Cartigny, D.1
Nagano, T.2
Ayad, T.3
Genet, J.P.4
Ohshima, T.5
Mashima, K.6
Ratovelomanana-Vidal, V.7
46
33751155033
Ohta T, Miyake T, Seido N, Kumobayashi H, Takaya H, J. Org. Chem. 1995 60 357
(1995)
J. Org. Chem.
, vol.60
, pp. 357
Ohta, T.1
Miyake, T.2
Seido, N.3
Kumobayashi, H.4
Takaya, H.5
48
33748929853
Feiertag P, Albert M, Nettekoven U, Spindler F, Org. Lett. 2006 8 4133
(2006)
Org. Lett.
, vol.8
, pp. 4133
Feiertag, P.1
Albert, M.2
Nettekoven, U.3
Spindler, F.4
49
0034619233
Raynor S A., Thomas J M., Raja R, Johnson B F. G., Belle R G., Mantle M D., Chem. Commun. 2000 1925
(2000)
Chem. Commun.
, pp. 1925
Raynor, S.A.1
Thomas, J.M.2
Raja, R.3
Johnson, B.F.G.4
Belle, R.G.5
Mantle, M.D.6
50
4344711567
Glorius F, Spielkamp N, Holle S, Goddard R, Lehmann C W., Angew. Chem. Int. Ed. 2004 43 2850
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 2850
Glorius, F.1
Spielkamp, N.2
Holle, S.3
Goddard, R.4
Lehmann, C.W.5
53
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
54
3142732882
Kuwano R, Kaneda K, Ito T, Sato K, Kurokawa T, Ito Y, Org. Lett. 2004 6 2213
(2004)
Org. Lett.
, vol.6
, pp. 2213
Kuwano, R.1
Kaneda, K.2
Ito, T.3
Sato, K.4
Kurokawa, T.5
Ito, Y.6
57
77954262931
Wang D.-S, Chen Q.-A, Li W, Yu C.-B, Zhou Y.-G, Zhang X M., 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.M.6
58
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
59
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
60
71649102649
[nl]
Wang D.-S, Zhou J, Wang D.-W, Guo Y.-L, Zhou [nl]Y.-G, Tetrahedron Lett. 2010 51 525
(2010)
Tetrahedron Lett.
, vol.51
, pp. 525
Wang, D.-S.1
Zhou, J.2
Wang, D.-W.3
Guo, Y.-L.4
Zhou, Y.-G.5
61
35348878469
Jahjah M, Alame M, Pellet-Rostaing S, Lemaire M, Tetrahedron: Asymmetry 2007 18 2305
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2305
Jahjah, M.1
Alame, M.2
Pellet-Rostaing, S.3
Lemaire, M.4
62
77951216702
Tang W.-J, Tan J, Xu L.-J, Lam K.-H, Fan Q.-H, Chan A S. C., Adv. Synth. Catal. 2010 352 1055
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1055
Tang, W.-J.1
Tan, J.2
Xu, L.-J.3
Lam, K.-H.4
Fan, Q.-H.5
Chan, A.S.C.6
63
77954674180
Tang W.-J, Sun Y.-W, Xu L.-J, Wang T.-L, Fan Q.-H, Lam K.-H, Chan A S. C., Org. Biomol. Chem. 2010 8 3464
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 3464
Tang, W.-J.1
Sun, Y.-W.2
Xu, L.-J.3
Wang, T.-L.4
Fan, Q.-H.5
Lam, K.-H.6
Chan, A.S.C.7
64
70449393264
Mamat C, Flemming A, Köckerling M, Steinbach J, Wuest F R., Synthesis 2009 3311
(2009)
Synthesis
, pp. 3311
Mamat, C.1
Flemming, A.2
Köckerling, M.3
Steinbach, J.4
Wuest, F.R.5