-
1
-
-
29144521717
-
-
For reviews, see: and references cited therein
-
For reviews, see:. Glorius F. Org. Biomol. Chem. 3 (2005) 4171 and references cited therein
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 4171
-
-
Glorius, F.1
-
3
-
-
0011592742
-
-
For asymmetric hydrogenation of 2-methylquinoxaline, see:
-
For asymmetric hydrogenation of 2-methylquinoxaline, see:. Bianchini C., Barbaro P., and Scapacci G. J. Organomet. Chem. 621 (2001) 26
-
(2001)
J. Organomet. Chem.
, vol.621
, pp. 26
-
-
Bianchini, C.1
Barbaro, P.2
Scapacci, G.3
-
4
-
-
0037806851
-
-
Henschke J.P., Burk M.J., Malan C.G., Herzberg D., Peterson J.A., Wildsmith A.J., Cobley C.J., and Casy G. Adv. Synth. Catal. 345 (2003) 300
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 300
-
-
Henschke, J.P.1
Burk, M.J.2
Malan, C.G.3
Herzberg, D.4
Peterson, J.A.5
Wildsmith, A.J.6
Cobley, C.J.7
Casy, G.8
-
5
-
-
0000218673
-
-
Bianchini C., Barbaro P., Scapacci G., Farnetti E., and Graziani M. Organometallics 17 (1998) 3308
-
(1998)
Organometallics
, vol.17
, pp. 3308
-
-
Bianchini, C.1
Barbaro, P.2
Scapacci, G.3
Farnetti, E.4
Graziani, M.5
-
7
-
-
0034625892
-
-
For asymmetric hydrogenation of indoles, see:
-
For asymmetric hydrogenation of indoles, see:. Kuwano R., Sato K., Kurokawa T., Karube D., and Ito Y. J. Am. Chem. Soc. 122 (2000) 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
-
8
-
-
3142732882
-
-
Kuwano R., Kaneda K., Ito T., Sato K., Kurokawa T., and Ito Y. Org. Lett. 6 (2004) 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
-
9
-
-
33645913553
-
-
Kuwano R., Kashiwabara M., Sato K., Ito T., Kaneda K., and Ito Y. Tetrahedron: Asymmetry 17 (2006) 521
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 521
-
-
Kuwano, R.1
Kashiwabara, M.2
Sato, K.3
Ito, T.4
Kaneda, K.5
Ito, Y.6
-
11
-
-
4344711567
-
-
For asymmetric hydrogenation of pyridines, see:
-
For asymmetric hydrogenation of pyridines, see:. Glorius F., Spielkamp N., Holle S., Goddard R., and Lehmann C.W. Angew. Chem. Int. Ed. 43 (2004) 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
-
14
-
-
0000093414
-
-
Trost B.M., and Fleming I. (Eds), Pergamon, Oxford
-
Keay J.D. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis vol. 8 (1991), Pergamon, Oxford 579
-
(1991)
Comprehensive Organic Synthesis
, vol.8
, pp. 579
-
-
Keay, J.D.1
-
16
-
-
34249294595
-
-
Barton D.H.R., Nakanishi K., and Meth-Cohn O. (Eds), Elsevier, Oxford
-
In: Barton D.H.R., Nakanishi K., and Meth-Cohn O. (Eds). Comprehensive Natural Products Chemistry (1999), Elsevier, Oxford 1-9
-
(1999)
Comprehensive Natural Products Chemistry
, pp. 1-9
-
-
-
17
-
-
0032777223
-
-
Jacquemond-Collet I., Hannedouche S., Fabre N., Fouraste I., and Moulis C. Phytochemistry 51 (1999) 1167
-
(1999)
Phytochemistry
, vol.51
, pp. 1167
-
-
Jacquemond-Collet, I.1
Hannedouche, S.2
Fabre, N.3
Fouraste, I.4
Moulis, C.5
-
18
-
-
33746347606
-
-
Rokotoson J.H., Fabre N., Jacquemond-Collet I., Hannedouche S., Fabre N., Fouraste I., and Moulis C. Planta Med. 64 (1998) 760
-
(1998)
Planta Med.
, vol.64
, pp. 760
-
-
Rokotoson, J.H.1
Fabre, N.2
Jacquemond-Collet, I.3
Hannedouche, S.4
Fabre, N.5
Fouraste, I.6
Moulis, C.7
-
20
-
-
0034833670
-
-
Jacquemond-Collet I., Bessiere J.M., Hannedouche S., Bertrand C., Fouraste I., and Moulis C. Phytochem. Anal. 12 (2001) 312
-
(2001)
Phytochem. Anal.
, vol.12
, pp. 312
-
-
Jacquemond-Collet, I.1
Bessiere, J.M.2
Hannedouche, S.3
Bertrand, C.4
Fouraste, I.5
Moulis, C.6
-
24
-
-
0001714846
-
-
Baralt E., Smith S.J., Hurwitz J., Horvath I.T., and Fish R.H. J. Am. Chem. Soc. 114 (1992) 5187
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 5187
-
-
Baralt, E.1
Smith, S.J.2
Hurwitz, J.3
Horvath, I.T.4
Fish, R.H.5
-
26
-
-
0021499845
-
-
Watanabe Y., Ohta T., Tsuji Y., Hiyoshi T., and Tsuji Y. Bull. Chem. Soc. Jpn. 57 (1984) 2440
-
(1984)
Bull. Chem. Soc. Jpn.
, vol.57
, pp. 2440
-
-
Watanabe, Y.1
Ohta, T.2
Tsuji, Y.3
Hiyoshi, T.4
Tsuji, Y.5
-
30
-
-
0041825591
-
-
For our own work, see:
-
For our own work, see:. Wang W.-B., Lu S.-M., Yang P.-Y., Han X.-W., and Zhou Y.-G. J. Am. Chem. Soc. 125 (2003) 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
-
33
-
-
16644386624
-
-
Other's work, see:
-
Other's work, see:. Xu L.-J., Lam K.H., Ji J.-X., Fan Q.-H., Lo W.-H., and 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
-
34
-
-
28244476491
-
-
Lam K.H., Xu L.-J., Feng L.-C., Fan Q.-H., Lam F.L., Lo W.-H., and Chan A.S.C. Adv. Synth. Catal. 347 (2005) 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
-
35
-
-
33646677236
-
-
Qiu L.-Q., Kwong F.Y., Wu J., Lam W.H., Chan C., Yu W.-Y., Li Y.-M., Guo R., Zhou Z.-Y., and Chan A.S.C. J. Am. Chem. Soc. 128 (2006) 5955
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5955
-
-
Qiu, L.-Q.1
Kwong, F.Y.2
Wu, J.3
Lam, W.H.4
Chan, C.5
Yu, W.-Y.6
Li, Y.-M.7
Guo, R.8
Zhou, Z.-Y.9
Chan, A.S.C.10
-
38
-
-
33846816454
-
-
Tang W.-J., Zhu S.-F., Xu L.-J., Zhou Q.-L., Fan Q.-H., Zhou H.-F., Lam K., and Chan A.S.C. Chem. Commun. (2007) 613-615
-
(2007)
Chem. Commun.
, pp. 613-615
-
-
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
-
39
-
-
34147102783
-
-
Wang Z.-J., Deng G.-J., Li Y., He Y.-M., Tang W.-J., and Fan Q.-H. Org. Lett. 9 (2007) 1243-1246
-
(2007)
Org. Lett.
, vol.9
, pp. 1243-1246
-
-
Wang, Z.-J.1
Deng, G.-J.2
Li, Y.3
He, Y.-M.4
Tang, W.-J.5
Fan, Q.-H.6
-
40
-
-
9644281424
-
-
For reviews see:
-
For reviews see:. Maitlis P.M., Haynes A., James B.R., Catellani M., and Chiusoli G.P. Dalton Trans. (2004) 3409
-
(2004)
Dalton Trans.
, pp. 3409
-
-
Maitlis, P.M.1
Haynes, A.2
James, B.R.3
Catellani, M.4
Chiusoli, G.P.5
-
44
-
-
34249282090
-
-
note
-
When the S/C is 1000/1, using KI and LiI as the additive, the conversions in THF are 37% and 34%, respectively.
-
-
-
-
45
-
-
34249294118
-
-
note
-
2 as the metal precursor with the following chiral ligands in THF in the presence of iodine: (R,R)-Me-DuPhos, (R)-MeO-BiPhep and (R)-BINAP. These reactions gave product 2a with good yields, but the enantioselectivities were very low (<2% ee).
-
-
-
|