-
1
-
-
70349935878
-
-
For a general overview of the reduction of imines, see the following
-
For a general overview of the reduction of imines, see the following:
-
-
-
-
9
-
-
70349941951
-
-
For hydrosilylation, see, e.g
-
For hydrosilylation, see, e.g.:
-
-
-
-
17
-
-
70349935880
-
-
For transfer hydrogenation, see, e.g
-
For transfer hydrogenation, see, e.g.:
-
-
-
-
20
-
-
33749521436
-
-
Zhu S.-F., Xie J.-B., Zhang Y.-Z., Li S., and Zhou Q.-L. J. Am. Chem. Soc. 128 (2006) 12886
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(2006)
J. Am. Chem. Soc.
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Zhu, S.-F.1
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Zhang, Y.-Z.3
Li, S.4
Zhou, Q.-L.5
-
22
-
-
70349899693
-
-
For an overview, see
-
For an overview, see:
-
-
-
-
24
-
-
70349933728
-
-
For the kinetic resolution using transfer hydrogenation combined with an ezymatic reaction, see
-
For the kinetic resolution using transfer hydrogenation combined with an ezymatic reaction, see:
-
-
-
-
26
-
-
33750702516
-
-
Samec J.S.M., Éll A.H., Åberg J.B., Privalov T., Eriksson L., and Bäckvall J.-E. J. Am. Chem. Soc. 128 (2006) 14293
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Samec, J.S.M.1
Éll, A.H.2
Åberg, J.B.3
Privalov, T.4
Eriksson, L.5
Bäckvall, J.-E.6
-
29
-
-
70349905804
-
-
2H, Ru, see
-
2H, Ru), see:
-
-
-
-
31
-
-
0030944755
-
-
Schinder P., Kock G., Pretot R., Wang G., Bohnen F.,M., Kruger C., and Pfaltz A. Chem.-Eur. J. 3 (1997) 887
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Schinder, P.1
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Bohnen, F.,M.5
Kruger, C.6
Pfaltz, A.7
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32
-
-
70349930534
-
-
For recent reports on catalytic hydrogenation (with Ti, Ir, Rh, and Ru), see Refs. 1b-d and the following:
-
For recent reports on catalytic hydrogenation (with Ti, Ir, Rh, and Ru), see Refs. 1b-d and the following:
-
-
-
-
34
-
-
0041808241
-
-
Jiang X.B., Minnaard A.J., Hessen B., Feringa B.L., Duchateau A.L.L., Andrien J.G.O., Boogers J.A.F., and de Vries J.G. Org. Lett. 5 (2003) 1503
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Jiang, X.B.1
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Duchateau, A.L.L.5
Andrien, J.G.O.6
Boogers, J.A.F.7
de Vries, J.G.8
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38
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0242458417
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Cobbley C.J., Foucher E., Lecouve J.-P., Lennon I.C., Ramsden J.A., and Thominot G. Tetrahedron: Asymmetry 14 (2003) 3431
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(2003)
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Cobbley, C.J.1
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Lennon, I.C.4
Ramsden, J.A.5
Thominot, G.6
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43
-
-
70349924522
-
-
For Rh-catalyzed hydrogenation of enamides, see the following
-
For Rh-catalyzed hydrogenation of enamides, see the following:
-
-
-
-
45
-
-
70349149690
-
-
Yiang Q., Gao W., Deng J., and Zhang X. Angew. Chem., Int. Ed. 45 (2006) 2832
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(2006)
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Yiang, Q.1
Gao, W.2
Deng, J.3
Zhang, X.4
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47
-
-
70349919217
-
-
For the activation of trichlorosilyl reagents by Lewis bases, see the following
-
For the activation of trichlorosilyl reagents by Lewis bases, see the following:
-
-
-
-
48
-
-
84891036468
-
Chiral Lewis Bases as Catalysts
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Dalko P.I. (Ed), Wiley-VCH, Weinheim
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Kočovský P., and Malkov A.V. Chiral Lewis Bases as Catalysts. In: Dalko P.I. (Ed). Enantioselective Organocatalysis (2007), Wiley-VCH, Weinheim 255
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(2007)
Enantioselective Organocatalysis
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Kočovský, P.1
Malkov, A.V.2
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49
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84891014400
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Organocatalytic Enantioselective Reduction of Olefins, Ketones, and Imines
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Dalko P.I. (Ed), Wiley-VCH, Weinheim
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Kagan H. Organocatalytic Enantioselective Reduction of Olefins, Ketones, and Imines. In: Dalko P.I. (Ed). Enantioselective Organocatalysis (2007), Wiley-VCH, Weinheim 391
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(2007)
Enantioselective Organocatalysis
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Kagan, H.1
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52
-
-
70349908933
-
-
For a different approach, employing a chiral Brønsted acid as catalyst and Hantzsch dihydropyridine as a reducing agent, see the following
-
For a different approach, employing a chiral Brønsted acid as catalyst and Hantzsch dihydropyridine as a reducing agent, see the following:
-
-
-
-
54
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24044465512
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Rueping M., Sugiono E., Azap C., Theissmann T., and Bolte M. Org. Lett. 7 (2005) 3781
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Iwasaki F., Onomura O., Mishima K., Kanematsu T., Maki T., and Matsumura Y. Tetrahedron Lett. 42 (2001) 2525
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(2001)
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Wang Z., Cheng M., Wu P., Wei S., and Sun J. Org. Lett. 8 (2006) 3045
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(2006)
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Wang, Z.1
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(2006)
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Wu P., Wang Z., Cheng M., Zhou L., and Sun J. Tetrahedron 64 (2008) 11304
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(2008)
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Wu, P.1
Wang, Z.2
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Zhou, L.4
Sun, J.5
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71
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-
70349905803
-
-
For other amides, see
-
For other amides, see:
-
-
-
-
73
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55449085483
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Zheng H.-J., Chen W.B., Wu Z.-J., Deng J.-G., Lin W.-Q., Yuan W.-C., and Zhang X.-M. Chem.-Eur. J. 14 (2008) 9864
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(2008)
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Zheng, H.-J.1
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Lin, W.-Q.5
Yuan, W.-C.6
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Guizzetti S., Benaglia M., Cozzi F., Rossi S., and Celentano G. Chirality 21 (2009) 233
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(2009)
Chirality
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Benaglia, M.2
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Rossi, S.4
Celentano, G.5
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Malkov A.V., Stončius S., MacDougall K.N., Mariani A., McGeoch G.D., and Kočovský P. Tetrahedron 62 (2006) 264
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(2006)
Tetrahedron
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Malkov, A.V.1
Stončius, S.2
MacDougall, K.N.3
Mariani, A.4
McGeoch, G.D.5
Kočovský, P.6
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81
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53849083142
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Malkov A.V., Stončius S., Vranková K., Arndt M., and Kočovský P. Chem.-Eur. J. 14 (2008) 8082
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(2008)
Chem.-Eur. J.
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Malkov, A.V.1
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Arndt, M.4
Kočovský, P.5
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83
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70350721187
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doi:10.1002/chem.200901573;
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Malkov, A. V.; Figlus, M.; Prestly, M. R.; Rabani, G.; Cooke, G.; Kočovský, P. Chem.-Eur. J. 2009, 15, doi:10.1002/chem.200901573;
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Chem.-Eur. J
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Malkov, A.V.1
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Prestly, M.R.3
Rabani, G.4
Cooke, G.5
Kočovský, P.6
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84
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64649102928
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Malkov A.V., Figlus M., Cooke G., Caldwell S.T., Rabani G., Prestly M.R., and Kočovský P. Org. Biomol. Chem. (2009) 1878
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(2009)
Org. Biomol. Chem.
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Malkov, A.V.1
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Cooke, G.3
Caldwell, S.T.4
Rabani, G.5
Prestly, M.R.6
Kočovský, P.7
-
85
-
-
70349933729
-
-
in preparation
-
Cooke, G.; Figlus, M.; Caldwell, S. T.; Walas, D.; Sanyal, A.; Yesilbag, G.; Malkov, A. V.; Kočovský, P., in preparation.
-
-
-
Cooke, G.1
Figlus, M.2
Caldwell, S.T.3
Walas, D.4
Sanyal, A.5
Yesilbag, G.6
Malkov, A.V.7
Kočovský, P.8
-
86
-
-
70349922352
-
-
3SiH, catalyzed by metal-free Lewis bases, see:
-
3SiH, catalyzed by metal-free Lewis bases, see:
-
-
-
-
87
-
-
0033569979
-
-
Iwasaki F., Onomura O., Mishima K., Maki T., and Matsumura Y. Tetrahedron Lett. 40 (1999) 7507
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(1999)
Tetrahedron Lett.
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Iwasaki, F.1
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Mishima, K.3
Maki, T.4
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33748596087
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Matsumura Y., Ogura K., Kouchi Y., Iwasaki F., and Onomura O. Org. Lett. 8 (2006) 3789
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(2006)
Org. Lett.
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Matsumura, Y.1
Ogura, K.2
Kouchi, Y.3
Iwasaki, F.4
Onomura, O.5
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89
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33745661731
-
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Malkov A.V., Stewart Liddon A.J.P., Ramírez-López P., Bendová L., Haigh D., and Kočovský P. Angew. Chem., Int. Ed. 45 (2006) 1432
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Stewart Liddon, A.J.P.2
Ramírez-López, P.3
Bendová, L.4
Haigh, D.5
Kočovský, P.6
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92
-
-
70349919218
-
-
For the method, see, e.g., Refs. 11c,e and 13.
-
For the method, see, e.g., Refs. 11c,e and 13.
-
-
-
-
93
-
-
70349945075
-
-
note
-
13 However, in the coupling reaction, the dibromide should act as an electrophile, which is a role better suited to the electron-poor nitro derivative 6 than to its amino analogue.
-
-
-
-
94
-
-
70349901785
-
-
See Ref. 11b and the following:
-
See Ref. 11b and the following:
-
-
-
-
98
-
-
0028201818
-
-
Pitzele B.S., Hamilton R.W., Kudla K.D., Tsymbalov S., Stapelfeld A., Savage M.A., Clare M., Hammond D.L., and Hansen D.W. J. Med. Chem. 37 (1994) 888
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Kudla, K.D.3
Tsymbalov, S.4
Stapelfeld, A.5
Savage, M.A.6
Clare, M.7
Hammond, D.L.8
Hansen, D.W.9
-
101
-
-
70349903850
-
-
note
-
11f,g
-
-
-
|