-
1
-
-
0003905731
-
-
Academic, New York
-
For a general overview of the reduction of imines, see the following: (a) J. D. Morrison, Asymmetric Synthesis, Academic, New York, 1983, vol.2;
-
(1983)
Asymmetric Synthesis
, vol.2
-
-
Morrison, J.D.1
-
3
-
-
84891580093
-
-
J. Wiley, and Sons, New York, 2nd edn
-
(c) I. Ojima, Catalytic Asymmetric Synthesis, J. Wiley, and Sons, New York, 2nd edn, 2000;
-
(2000)
Catalytic Asymmetric Synthesis
-
-
Ojima, I.1
-
6
-
-
33745592483
-
-
(f) B. T. Cho, Tetrahedron, 2006, 62, 7621;
-
(2006)
Tetrahedron
, vol.62
, pp. 7621
-
-
Cho, B.T.1
-
7
-
-
0003445429
-
-
Springer, Berlin
-
(g) E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Comprehensive Asymmetric Catalysis, Springer, Berlin, 1999, vol.I-III.
-
(1999)
Comprehensive Asymmetric Catalysis
, vol.1-3
-
-
Jacobsen, E.N.1
Pfaltz, A.2
Yamamoto, H.3
-
8
-
-
0035903688
-
-
For recent reports on catalytic hydrogenation (with Ti, Ir, Rh and Ru), see ref. 1b-d and the following: (a) D. Xiao and X. Zhang, Angew. Chem., Int. Ed, 2001, 40, 3425;
-
(2001)
Angew. Chem., Int. Ed
, vol.40
, pp. 3425
-
-
Xiao, D.1
Zhang, X.2
-
9
-
-
0041808241
-
-
(b) X. B. Jiang, A. J. Minnaard, B. Hessen, B. L. Feringa, A. L. L. Duchateau, J. G. O. Andrien, J. A. F. Boogers and J. G. de Vries, Org. Lett., 2003, 5, 1503;
-
(2003)
Org. Lett.
, vol.5
, pp. 1503
-
-
Jiang, X.B.1
Minnaard, A.J.2
Hessen, B.3
Feringa, B.L.4
Duchateau, A.L.L.5
Andrien, J.G.O.6
Boogers, J.A.F.7
De Vries, J.G.8
-
11
-
-
0034733071
-
-
(d) J.Okuda, S. Verch, R. Stürmer and T. S. Spaniol, J. Organomet. Chem., 2000, 605, 55;
-
(2000)
J. Organomet. Chem.
, vol.605
, pp. 55
-
-
Okuda, J.1
Verch, S.2
Stürmer, R.3
Spaniol, T.S.4
-
12
-
-
0242439584
-
-
(e) E. Guiu, B. Muñoz, S. Castillón and C. Claver, Adv. Synth. Catal, 2003, 345, 169;
-
(2003)
Adv. Synth. Catal
, vol.345
, pp. 169
-
-
Guiu, E.1
Muñoz, B.2
Castillón, S.3
Claver, C.4
-
13
-
-
0242458417
-
-
(f) C. J. Cobley, E. Foucher, J.-P. Lecouve, I. C. Lennon, J. A. Ramsden and G. Thominot, Tetrahedron: Asymmetry, 2003, 14, 3431;
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 3431
-
-
Cobley, C.J.1
Foucher, E.2
Lecouve, J.-P.3
Lennon, I.C.4
Ramsden, J.A.5
Thominot, G.6
-
14
-
-
0038626742
-
-
(g) Y. Chi, Y. G. Zhou and X. Zhang, J. Org. Chem., 2003, 68, 4120;
-
(2003)
J. Org. Chem.
, vol.68
, pp. 4120
-
-
Chi, Y.1
Zhou, Y.G.2
Zhang, X.3
-
15
-
-
0345306324
-
-
(h) A. A. Boezio, J. Pytkowicz, A. Côté and A. B. Charette, J. Am. Chem. Soc., 2003, 125, 14260;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 14260
-
-
Boezio, A.A.1
Pytkowicz, J.2
Côté, A.3
Charette, A.B.4
-
16
-
-
7044229833
-
-
(i) A. Trifonova, J. S. Diesen, C. J. Chapman and P. G. Andersson, Org. Lett, 2004, 6, 3825;
-
(2004)
Org. Lett
, vol.6
, pp. 3825
-
-
Trifonova, A.1
Diesen, J.S.2
Chapman, C.J.3
Andersson, P.G.4
-
17
-
-
33749521436
-
-
(j) S.-F. Zhu, J.-B. Xie, Y.-Z. Zhang, S. Li and Q.-L. Zhou, J. Am. Chem. Soc., 2006, 128, 12886;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 12886
-
-
Zhu, S.-F.1
Xie, J.-B.2
Zhang, Y.-Z.3
Li, S.4
Zhou, Q.-L.5
-
18
-
-
33644749156
-
-
(k) A. Trifonova, J. S. Diesen and P. G. Andersson, Chem.-Eur. J., 2006, 12, 2318.
-
(2006)
Chem.-Eur. J.
, vol.12
, pp. 2318
-
-
Trifonova, A.1
Diesen, J.S.2
Andersson, P.G.3
-
19
-
-
6444241533
-
-
For Rh-catalysed hydrogenation of enamides, see the following: X.-P. Hu and Z. Zheng, Org. Lett., 2004, 6, 3585.
-
(2004)
Org. Lett.
, vol.6
, pp. 3585
-
-
Hu, X.-P.1
Zheng, Z.2
-
21
-
-
0345276532
-
-
(b) R. Kadyrov and T. H. Riermeier, Angew. Chem., Int. Ed, 2003, 42, 5472;
-
(2003)
Angew. Chem., Int. Ed
, vol.42
, pp. 5472
-
-
Kadyrov, R.1
Riermeier, T.H.2
-
22
-
-
33749521436
-
-
(c) S.-F. Zhu, J.-B. Xie, Y.-Z. Zhang, S. Li and Q.-L. Zhou, J. Am. Chem. Soc., 2006, 128, 12886;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 12886
-
-
Zhu, S.-F.1
Xie, J.-B.2
Zhang, Y.-Z.3
Li, S.4
Zhou, Q.-L.5
-
23
-
-
33745493944
-
-
For an overview, see
-
(d) J. B. Åberg, J. S. M. Samec and J.-E. Bäckvall, Chem. Commun., 2006, 2771. For an overview, see:
-
(2006)
Chem. Commun.
, pp. 2771
-
-
Åberg, J.B.1
Samec, J.S.M.2
Bäckvall, J.-E.3
-
24
-
-
33644660116
-
-
For the kinetic resolution using transfer hydrogénation combined with an enzymatic reaction, see
-
(e) J. S. M. Samec, J.-E. Bäckvall, P. G. Andersson and P. Brandt, Chem. Soc. Rev., 2006, 35, 237. For the kinetic resolution using transfer hydrogénation combined with an enzymatic reaction, see:
-
(2006)
Chem. Soc. Rev.
, vol.35
, pp. 237
-
-
Samec, J.S.M.1
Bäckvall, J.-E.2
Andersson, P.G.3
Brandt, P.4
-
26
-
-
33750702516
-
-
(g) J. S. M. Samec, A. H. Éll, J. B. Åberg, T. Privalov, L. Eriksson and J.-E. Bäckvall, J Am. Chem. Soc., 2006, 128, 14293;
-
(2006)
J Am. Chem. Soc.
, vol.128
, pp. 14293
-
-
Samec, J.S.M.1
Éll, A.H.2
Åberg, J.B.3
Privalov, T.4
Eriksson, L.5
Bäckvall, J.-E.6
-
27
-
-
34249938172
-
-
(h) T. Privalov, J. S. M. Samec and J.-E. Bäckvall, Organometallics, 2007, 26, 2840;
-
(2007)
Organometallics
, vol.26
, pp. 2840
-
-
Privalov, T.1
Samec, J.S.M.2
Bäckvall, J.-E.3
-
28
-
-
37849035610
-
-
(i) C. E. Hoben, L. Kanupp and J.-E. Bäckvall, Tetrahedron Lett., 2008, 49, 977.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 977
-
-
Hoben, C.E.1
Kanupp, L.2
Bäckvall, J.-E.3
-
30
-
-
0032482056
-
-
(b) X. Verdaguer, U. E. W. Lange and S. L. Buchwald, Angew. Chem., Int. Ed, 1998, 37, 1103;
-
(1998)
Angew. Chem., Int. Ed
, vol.37
, pp. 1103
-
-
Verdaguer, X.1
Lange, U.E.W.2
Buchwald, S.L.3
-
32
-
-
0032885955
-
-
(d) E. Vedejs, P. Trapencieris and E. Suna, J. Org. Chem., 1999, 64, 6724;
-
(1999)
J. Org. Chem.
, vol.64
, pp. 6724
-
-
Vedejs, E.1
Trapencieris, P.2
Suna, E.3
-
34
-
-
0035956540
-
-
(f) B. H. Lipshutz, K. Noson and W. Chrisman, J Am. Chem. Soc.,2001, 123, 12917;
-
(2001)
J Am. Chem. Soc.
, vol.123
, pp. 12917
-
-
Lipshutz, B.H.1
Noson, K.2
Chrisman, W.3
-
35
-
-
3142710052
-
-
(g) B.H. Lipshutz and H. Shimizu, Angew. Chem., Int. Ed., 2004, 43, 2228.
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 2228
-
-
Lipshutz, B.H.1
Shimizu, H.2
-
36
-
-
0037008967
-
-
For enzymatic approaches, including reduction, see, e.g.: (a) M. Alexeeva, A. Enright, M. J. Dawson, M. Mahmoidian and N. J. Turner, Angew. Chem., Int. Ed, 2002, 41, 3177;
-
(2002)
Angew. Chem., Int. Ed
, vol.41
, pp. 3177
-
-
Alexeeva, M.1
Enright, A.2
Dawson, M.J.3
Mahmoidian, M.4
Turner, N.J.5
-
37
-
-
21044439352
-
-
(b) R. Carr, M. Alexeeva, M. J. Dawson, V. Gotor-Fernández, C. E. Huphrey and N. J. Turner, ChemBioChem, 2005, 6, 637;
-
(2005)
ChemBioChem
, vol.6
, pp. 637
-
-
Carr, R.1
Alexeeva, M.2
Dawson, M.J.3
Gotor-Fernández, V.4
Huphrey, C.E.5
Turner, N.J.6
-
38
-
-
33644523056
-
-
For a brief overview, see
-
(c) C. J. Dunsmore, R. Carr, T. Fleming and N. J. Turner, J. Am. Chem. Soc., 2006, 128, 2224. For a brief overview, see:
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 2224
-
-
Dunsmore, C.J.1
Carr, R.2
Fleming, T.3
Turner, N.J.4
-
39
-
-
0346780250
-
-
(d) M. Alexeeva, R. Carr and N. J. Turner, Org. Biomol. Chem., 2003, 1, 4133.
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 4133
-
-
Alexeeva, M.1
Carr, R.2
Turner, N.J.3
-
40
-
-
30744457769
-
-
(a) S. Singh and U. K. Batra, Indian J. Chem, Sect. B, 1989, 28, 1;
-
(1989)
Indian J. Chem, Sect. B
, vol.28
, pp. 1
-
-
Singh, S.1
Batra, U.K.2
-
41
-
-
24044465512
-
-
(b) M. Rueping, E. Sugiono, C. Azap, T. Theissmann and M. Bolte, Org. Lett., 2005, 7, 3781;
-
(2005)
Org. Lett.
, vol.7
, pp. 3781
-
-
Rueping, M.1
Sugiono, E.2
Azap, C.3
Theissmann, T.4
Bolte, M.5
-
42
-
-
33746269442
-
-
(c) M. Rueping, A. P. Antonchick and T. Theissmann, 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
-
43
-
-
33750148995
-
-
(d) M. Rueping, A. P. Antonchik and T. Theissmann, Angew. Chem., Int. Ed., 2006, 45, 6751;
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 6751
-
-
Rueping, M.1
Antonchik, A.P.2
Theissmann, T.3
-
44
-
-
28044438742
-
-
(e) S. Hoffmann, A. M. Seayad and B. List, Angew. Chem., Int. Ed, 2005, 44, 7424;
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 7424
-
-
Hoffmann, S.1
Seayad, A.M.2
List, B.3
-
45
-
-
33749534513
-
-
(f) S. Hoffmann, M. Nicoletti and B. List, J. Am. Chem. Soc., 2006, 128, 13074;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13074
-
-
Hoffmann, S.1
Nicoletti, M.2
List, B.3
-
47
-
-
30744477746
-
-
(h) R. I. Storer, D. E. Carrera, Y. Ni and D. W. C. MacMillan, J. Am. Chem. Soc., 2006, 128, 84;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 84
-
-
Storer, R.I.1
Carrera, D.E.2
Ni, Y.3
MacMillan, D.W.C.4
-
48
-
-
38049089797
-
-
(i) S. G. Ouellet, A. M. Walji and D. W. C. MacMillan, Acc. Chem. Res., 2007, 40, 1327.
-
(2007)
Acc. Chem. Res.
, vol.40
, pp. 1327
-
-
Ouellet, S.G.1
Walji, A.M.2
MacMillan, D.W.C.3
-
49
-
-
3142759422
-
-
(a) A. V. Malkov, A. Mariani, K. N. MacDougall and P. Kočovský, Org. Lett., 2004, 6, 2253;
-
(2004)
Org. Lett.
, vol.6
, pp. 2253
-
-
Malkov, V.1
Mariani, A.2
MacDougall, K.N.3
Kočovský, P.4
-
50
-
-
28944440055
-
-
(b) A. V. Malkov, S. Stončius, K. N. MacDougall, A. Mariani, G. D. McGeoch and P. Kočovský, Tetrahedron, 2006, 62, 264;
-
(2006)
Tetrahedron
, vol.62
, pp. 264
-
-
Malkov, A.V.1
Stončius, S.2
MacDougall, K.N.3
Mariani, A.4
McGeoch, G.D.5
Kočovský, P.6
-
51
-
-
33847051249
-
-
(c) A. V. Malkov, M. Figlus, S. Stončius and P. Kočovský, J. Org. Chem., 2007, 72, 1315;
-
(2007)
J. Org. Chem.
, vol.72
, pp. 1315
-
-
Malkov, A.V.1
Figlus, M.2
Stončius, S.3
Kočovský, P.4
-
52
-
-
34250807821
-
-
(d) A. V. Malkov, S. Stončius and P. Kočovský, Angew. Chem., Int. Ed, 2001, 46, 3722;
-
(2001)
Angew. Chem., Int. Ed
, vol.46
, pp. 3722
-
-
Malkov, V.1
Stončius, S.2
Kočovský, P.3
-
53
-
-
44949212976
-
-
(e) A. V. Malkov, M. Figlus and P. Kočovský, J. Org. Chem., 2008, 73, 3985;
-
(2008)
J. Org. Chem.
, vol.73
, pp. 3985
-
-
Malkov, A.V.1
Figlus, M.2
Kočovský, P.3
-
54
-
-
53849083142
-
-
(f) A.V. Malkov, S. Stončius, K. Vranková, M. Arndt and P. Kočovský, Chem.-Eur. J., 2008, 14, 8082;
-
(2008)
Chem.-Eur. J.
, vol.14
, pp. 8082
-
-
Malkov, A.V.1
Stončius, S.2
Vranková, K.3
Arndt, M.4
Kočovský, P.5
-
55
-
-
70349091866
-
-
(g) A. V. Malkov, K. Vranková, S. Stončius and P. Kočovský, J. Org. Chem., 2009, 74, 5839;
-
(2009)
J. Org. Chem.
, vol.74
, pp. 5839
-
-
Malkov, A.V.1
Vranková, K.2
Stončius, S.3
Kočovský, P.4
-
56
-
-
70349971153
-
-
(h) A. V. Malkov, K. Vranková, R. Sigerson, S. Stončius and P. Kočovský, Tetrahedron, 2009, 65, 9481;
-
(2009)
Tetrahedron
, vol.65
, pp. 9481
-
-
Malkov, A.V.1
Vranková, K.2
Sigerson, R.3
Stončius, S.4
Kočovský, P.5
-
57
-
-
64649102928
-
-
(i) A. V. Malkov, M. Figlus, G. Cooke, S. T. Caldwell, G. Rabani, M. R. Prestly and P. Kočovský, Org. Biomol. Chem., 2009, 7, 1878;
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 1878
-
-
Malkov, A.V.1
Figlus, M.2
Cooke, G.3
Caldwell, S.T.4
Rabani, G.5
Prestly, M.R.6
Kočovský, P.7
-
58
-
-
70350721187
-
-
(j) A. V. Malkov, M. Figlus, M. R. Prestly, G. Rabani, G. Cooke and P. Kočovský, Chem.Eur. J., 2009, 15, 9651.
-
(2009)
Chem.Eur. J.
, vol.15
, pp. 9651
-
-
Malkov, A.V.1
Figlus, M.2
Prestly, M.R.3
Rabani, G.4
Cooke, G.5
Kočovský, P.6
-
59
-
-
0035953044
-
-
For other Lewis-basic organocatalysts promoting imine reduction, see: (a) F. Iwasaki, O. Onomura, K. Mishima, T. Kanematsu, T. Maki and Y. Matsumura, Tetrahedron Lett., 2001, 42, 2525;
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 2525
-
-
Iwasaki, F.1
Onomura, O.2
Mishima, K.3
Kanematsu, T.4
Maki, T.5
Matsumura, Y.6
-
60
-
-
33646079612
-
-
(b) O. Onomura, Y. Kouchi, F. Iwasaki and Y. Matsumura, Tetrahedron Lett., 2006, 47, 3751;
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 3751
-
-
Onomura, O.1
Kouchi, Y.2
Iwasaki, F.3
Matsumura, Y.4
-
61
-
-
33644935536
-
-
(c) Z. Wang, X. Ye, S. Wei, P. Wu, A. Zhang and J. Sun, Org Lett., 2006, 8, 999;
-
(2006)
, vol.8
, pp. 999
-
-
Wang, Z.1
Ye, X.2
Wei, S.3
Wu, P.4
Zhang, A.5
Sun, J.6
Lett, O.7
-
62
-
-
33746638360
-
-
Z. Wang, M. Cheng, P. Wu, S. Wei and J. Sun, Org Lett., 2006, 8, 3045;
-
(2006)
Org Lett.
, vol.8
, pp. 3045
-
-
Wang, Z.1
Cheng, M.2
Wu, P.3
Wei, S.4
Sun, J.5
-
63
-
-
34247138259
-
-
(d) Z. Wang, S. Wei, C. Wang and J. Sun, Tetrahedron: Asymmetry, 2007, 18, 705;
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 705
-
-
Wang, Z.1
Wei, S.2
Wang, C.3
Sun, J.4
-
64
-
-
33846289229
-
-
(e) D. Pei, Z. Wang, S. Wei, Y. Zhang and J. Sun, Org Lett., 2006, 8, 5913;
-
(2006)
Org Lett.
, vol.8
, pp. 5913
-
-
Pei, D.1
Wang, Z.2
Wei, S.3
Zhang, Y.4
Sun, J.5
-
65
-
-
34447331272
-
-
(f) L. Zhou, Z. Wang, S. We and J. Sun, Chem. Commun., 2007, 2977;
-
(2007)
Chem. Commun.
, vol.2977
-
-
Zhou, L.1
Wang, Z.2
We, S.3
Sun, J.4
-
66
-
-
55049095134
-
-
(g) C. Wang, X. Wu, L. Zhou and J. Sun, Chem.-Eur. J, 2008, 14, 8789;
-
(2008)
Chem.-Eur. J
, vol.14
, pp. 8789
-
-
Wu, W.X.1
Zhou, L.2
Sun, J.3
-
67
-
-
54549102004
-
-
(h) P. Wu, Z. Wang, M. Cheng, L. Zhou and J. Sun, Tetrahedron, 2008, 64, 11304;
-
(2008)
Tetrahedron
, vol.64
, pp. 11304
-
-
Wu, P.1
Wang, Z.2
Cheng, M.3
Zhou, L.4
Sun, J.5
-
68
-
-
35148865184
-
-
(i) H. Zheng, J. Deng, W. Lin and X. Zhang, Tetrahedron Lett., 2007, 48, 7934;
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 7934
-
-
Zheng, H.1
Deng, J.2
Lin, W.3
Zhang, X.4
-
69
-
-
55449085483
-
-
(j) H.-J. Zheng, W. B. Chen, Z.-J. Wu, J.-G Deng, W.-Q. Lin, W.-C. Yuan and X.-M. Zhang, Chem.-Eur. J., 2008, 14, 9864;
-
(2008)
Chem.-Eur. J.
, vol.14
, pp. 9864
-
-
Zheng, H.-J.1
Chen, W.B.2
Wu, Z.-J.3
Deng, J.-G.4
Lin, W.-Q.5
Yuan, W.-C.6
Zhang, X.-M.7
-
70
-
-
59849094066
-
-
(k) S. Guizzetti, M. Benaglia, F. Cozzi, S. Rossi and G. Celentano, Chirality, 2009, 21, 233;
-
(2009)
Chirality
, vol.21
, pp. 233
-
-
Guizzetti, S.1
Benaglia, M.2
Cozzi, F.3
Rossi, S.4
Celentano, G.5
-
71
-
-
58049149158
-
-
(l) F. M. Gautier, S. Jones and S. J. Martin, Org. Biomol. Chem., 2009, 7, 229;
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 229
-
-
Gautier, F.M.1
Jones, S.2
Martin, S.J.3
-
73
-
-
0033569979
-
-
3SiH, catalysed by metalfree Lewis bases, see: (a) F. Iwasaki, O. Onomura, K. Mishima, T. Maki and Y. Matsumura, Tetrahedron Lett., 1999, 40, 7507;
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 7507
-
-
Iwasaki, F.1
Onomura, O.2
Mishima, K.3
Maki, T.4
Matsumura, Y.5
-
74
-
-
33748596087
-
-
(b) Y. Matsumura, K. Ogura, Y. Kouchi, F. Iwasaki and O. Onomura, Org. Lett., 2006, 8, 3789;
-
(2006)
Org. Lett.
, vol.8
, pp. 3789
-
-
Matsumura, Y.1
Ogura, K.2
Kouchi, Y.3
Iwasaki, F.4
Onomura, O.5
-
75
-
-
33745661731
-
-
(c) A. V. Malkov, A. Stewart, J. P. Liddon, P. Ramirez-Lopez, L. Bendová, D. Haigh and P. Kočovský, Angew. Chem., Int. Ed., 2006, 45, 1432.
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 1432
-
-
Malkov, A.V.1
Stewart, A.2
Liddon, J.P.3
Ramirez-Lopez, P.4
Bendová, L.5
Haigh, D.6
Kočovský, P.7
-
76
-
-
38149130635
-
-
For representative recent reviews focusing upon dendrimer/dendronbased catalysts, see, e.g.: (a) A.-M. Caminade, P. Servin, R. Laurent and J.-P. Majorai, Chem. Soc. Rev., 2008, 37, 56;
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 56
-
-
Caminade, A.-M.1
Servin, P.2
Laurent, R.3
Majorai, J.-P.4
-
77
-
-
34447127092
-
-
(b) R. Andres, E. de Jesús and J. C. Flores, New J. Chem., 2007, 31, 1161;
-
(2007)
New J. Chem.
, vol.31
, pp. 1161
-
-
Andres, R.1
De Jesús, E.2
Flores, J.C.3
-
79
-
-
33845453364
-
-
(d) A. Berger, R. J. M. Klein Gebbink and G. van Koten, Top. Organomet. Chem., 2006, 20, 1;
-
(2006)
Top. Organomet. Chem.
, vol.20
, pp. 1
-
-
Berger, A.1
Klein Gebbink, R.J.M.2
Van Koten, G.3
-
82
-
-
33746772178
-
-
For a review of the dendrimer effect in homogenous catalysis, see: B. Helms and J. M. J. Fréchet, Adv. Synth. Catal, 2006, 348, 1125.
-
(2006)
Adv. Synth. Catal
, vol.348
, pp. 1125
-
-
Helms, B.1
Fréchet, J.M.J.2
-
83
-
-
25844483744
-
-
For representative recent examples of dendrimer/dendron-based enantioselective catalysts, see the following: (a) E. Bellis and G. Kokotos, J. Mol. Catal. A: Chem., 2005, 241, 166;
-
(2005)
J. Mol. Catal. A: Chem.
, vol.241
, pp. 166
-
-
Bellis, E.1
Kokotos, G.2
-
84
-
-
13244255392
-
-
(b) Y.-C. Chen, T.-F. Wu, L. Jiang, J.-G. Deng, H. Liu, J. Zhu and Y.-Z. Jiang, J. Org. Chem., 2005, 70, 1006;
-
(2005)
J. Org. Chem.
, vol.70
, pp. 1006
-
-
Chen, Y.-C.1
Wu, T.-F.2
Jiang, L.3
Deng, J.-G.4
Liu, H.5
Zhu, J.6
Jiang, Y.-Z.7
-
85
-
-
33747002158
-
-
(c) Y. Li, X.-Y. Liu and G. Zhao, Tetrahedron: Asymmetry, 2006, 17, 2034;
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 2034
-
-
Li, Y.1
Liu, X.-Y.2
Zhao, G.3
-
86
-
-
34447092113
-
-
(d) L. Yin, R. Li, F. Wang, H. Wang, Y. Zheng, C. Wang and J. Ma, Tetrahedron: Asymmetry, 2007, 18, 1383;
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 1383
-
-
Yin, L.1
Li, R.2
Wang, F.3
Wang, H.4
Zheng, Y.5
Wang, C.6
Ma, J.7
-
87
-
-
34147102783
-
-
(e) Z.-J. Wang, G-J. Deng, Y. Li, Y.-M. He, W.-J. Tang and Q.-H. Fan, 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
-
89
-
-
34248993554
-
-
(g) R. Breslow, S. Wei and C. Kenesky, Tetrahedron, 2007, 63, 6317;
-
(2007)
Tetrahedron
, vol.63
, pp. 6317
-
-
Breslow, R.1
Wei, S.2
Kenesky, C.3
-
90
-
-
33846369772
-
-
(h) L. Routaboul, S. Vincendeau, C.-O. Turrin, A.-M. Caminade, J.-P. Majorai, J.-C. Daran and E. Manoury, J. Organomet. Chem., 2001, 692, 1064;
-
(2001)
J. Organomet. Chem.
, vol.692
, pp. 1064
-
-
Routaboul, L.1
Vincendeau, S.2
Turrin, C.-O.3
Caminade, A.-M.4
Majorai, J.-P.5
Daran, J.-C.6
Manoury, E.7
-
91
-
-
43149091436
-
-
(i) Y.-N. Niu, Z.-Y. Yan, G.-Q. Li, H.-L. Wei, G.-L. Gao, L.-Y. Wu and Y.-M. Liang, Tetrahedron: Asymmetry, 2008, 19, 912;
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 912
-
-
Niu, Y.-N.1
Yan, Z.-Y.2
Li, G.-Q.3
Wei, H.-L.4
Gao, G.-L.5
Wu, L.-Y.6
Liang, Y.-M.7
-
93
-
-
41749101491
-
-
(k) L.-I. Rodriguez, O. Rossell, M. Seco and Gk Müller, Organometallics, 2008, 27, 1328;
-
(2008)
Organometallics
, vol.27
, pp. 1328
-
-
Rodriguez, L.-I.1
Rossell, O.2
Seco, M.3
Müller, G.4
-
94
-
-
45749105171
-
-
(l) J. Yu, T. V. RajanBabu and J. R. Parquette, J. Am. Chem. Soc., 2008, 130, 7845;
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7845
-
-
Yu, J.1
Rajanbabu, T.V.2
Parquette, J.R.3
-
95
-
-
56749161385
-
-
(m) F. Zhang, Y. Li, Z.-W. Li, Y.-M. He, S.-F. Zhu, Q.-H. Fan and Q.-L. Zhou, Chem. Commun., 2008, 6048.
-
(2008)
Chem. Commun.
, pp. 6048
-
-
Zhang, F.1
Li, Y.2
Li, Z.-W.3
He, Y.-M.4
Zhu, S.-F.5
Fan, Q.-H.6
Zhou, Q.-L.7
-
97
-
-
76849094565
-
-
7/8.
-
7/8.
-
-
-
-
98
-
-
76849110879
-
-
At 5 mol% catalyst loading, the product after centrifugation is contaminated by less than 0.5% of the catalyst and can be further purified by chromatography or crystallization.
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At 5 mol% catalyst loading, the product after centrifugation is contaminated by less than 0.5% of the catalyst and can be further purified by chromatography or crystallization.
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