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1
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0038260520
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Recent reviews: a
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Recent reviews: (a) Blaser, H.-U.; Malan, C.; Pugin, B.; Spindler, F.; Steiner, H.; Studer, M. Adv. Synth. Catal. 2003, 345, 103-151.
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(2003)
Adv. Synth. Catal
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Blaser, H.-U.1
Malan, C.2
Pugin, B.3
Spindler, F.4
Steiner, H.5
Studer, M.6
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6
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0000218673
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Bianchini, C.; Barbaro, P.; Scapacci, G.; Farnetti, E.; Graziani, M. Organometallics 1998, 17, 3308-3310.
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Organometallics
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Bianchini, C.1
Barbaro, P.2
Scapacci, G.3
Farnetti, E.4
Graziani, M.5
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7
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0034625892
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(a) Kuwano, R.; Sato, K.; Kurokawa, T.; Karube, D.; Ito, Y. J. Am. Chem. Soc. 2000, 122, 7614-7615.
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(2000)
J. Am. Chem. Soc
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Kuwano, R.1
Sato, K.2
Kurokawa, T.3
Karube, D.4
Ito, Y.5
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8
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33645913553
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(b) Kuwano, R.; Kashiwabara, M.; Sato, K.; Ito, T.; Kaneda, K.; Ito, Y. Tetrahedron: Asymmetry 2006, 17, 521-535.
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Tetrahedron: Asymmetry
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Kuwano, R.1
Kashiwabara, M.2
Sato, K.3
Ito, T.4
Kaneda, K.5
Ito, Y.6
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10
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0041825591
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Representative examples: (a) Wang, W.-B.; Lu, S.-M.; Yang, P.-Y.; Han, X.-W.; Zhou, Y.-G. J. Am. Chem. Soc. 2003, 125, 10536-10537.
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Representative examples: (a) Wang, W.-B.; Lu, S.-M.; Yang, P.-Y.; Han, X.-W.; Zhou, Y.-G. J. Am. Chem. Soc. 2003, 125, 10536-10537.
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11
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33745576403
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(b) Lu, S.-M.; Wang, Y.-Q.; Han, X.-W.; Zhou, Y.-G. Angew. Chem., Int. Ed. 2006, 45, 2260-2263.
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(2006)
Angew. Chem., Int. Ed
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Lu, S.-M.1
Wang, Y.-Q.2
Han, X.-W.3
Zhou, Y.-G.4
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13
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33846816454
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(d) 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, 613-615.
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(2007)
Chem. Commun
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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
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14
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33746269442
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High enantioselectivity was achieved in the reduction of quinolines with organocatalysis; see
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High enantioselectivity was achieved in the reduction of quinolines with organocatalysis; see: Rueping, M.; Antonchick, A. P.; Theissmann, T. Angew. Chem., Int. Ed. 2006, 45, 3683-3686.
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(2006)
Angew. Chem., Int. Ed
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Rueping, M.1
Antonchick, A.P.2
Theissmann, T.3
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16
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34250765230
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Very recently, high enantioselectivity has been reported in the organocatalytic transfer hydrogenation of pyridines; see
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Very recently, high enantioselectivity has been reported in the organocatalytic transfer hydrogenation of pyridines; see: Rueping, M.; Antonchick, A. P. Angew. Chem., Int. Ed. 2007, 46, 4562-4565.
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(2007)
Angew. Chem., Int. Ed
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, pp. 4562-4565
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Rueping, M.1
Antonchick, A.P.2
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17
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4344711567
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Highly stereoselective hydrogenation of pyridines modified with a chiral oxazolidinone with heterogeneous catalysis has been reported; see: Glorius, F, Spielkamp, N, Holle, S, Goddard, R, Lehmann, C. W. Angew. Chem, Int. Ed. 2004, 43, 2850-2852
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Highly stereoselective hydrogenation of pyridines modified with a chiral oxazolidinone with heterogeneous catalysis has been reported; see: Glorius, F.; Spielkamp, N.; Holle, S.; Goddard, R.; Lehmann, C. W. Angew. Chem., Int. Ed. 2004, 43, 2850-2852.
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18
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33747233073
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(a) Kaiser, S.; Smidt, S. P.; Pfaltz, A. Angew. Chem., Int. Ed. 2006, 45, 5194-5197.
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(2006)
Angew. Chem., Int. Ed
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Kaiser, S.1
Smidt, S.P.2
Pfaltz, A.3
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19
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33748929853
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(b) Feiertag, P.; Albert, M.; Nettekoven, U.; Spindler, F. Org. Lett. 2006, 8, 4133-4135.
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(2006)
Org. Lett
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Feiertag, P.1
Albert, M.2
Nettekoven, U.3
Spindler, F.4
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20
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0343289081
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Highly stereoselective hydrogenation of a pyrrole modified with chiral auxiliary had been reported; see: Hada, V, Tungler, A, Szepesy, L. Appl. Catal. A 2001, 210, 165-171
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Highly stereoselective hydrogenation of a pyrrole modified with chiral auxiliary had been reported; see: Hada, V.; Tungler, A.; Szepesy, L. Appl. Catal. A 2001, 210, 165-171.
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21
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0000920053
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(a) Sawamura, M.; Hamashima, H.; Sugawara, M.; Kuwano, R.; Ito, Y. Organometallics 1995, 14, 4549-4558.
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(1995)
Organometallics
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Sawamura, M.1
Hamashima, H.2
Sugawara, M.3
Kuwano, R.4
Ito, Y.5
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22
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38349134272
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Kuwano, R.; Sawamura, M. In Catalysts for Fine Chemical Synthesis, 5: Regio- and Stereo-Controlled Oxidations and Reductions; Roberts, S. M.; Whittall, J., Eds.; John Wiley & Sons: West Sussex, 2007; pp 73-86.
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(b) Kuwano, R.; Sawamura, M. In Catalysts for Fine Chemical Synthesis, Volume 5: Regio- and Stereo-Controlled Oxidations and Reductions; Roberts, S. M.; Whittall, J., Eds.; John Wiley & Sons: West Sussex, 2007; pp 73-86.
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23
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(a) Genêt, J. P.; Pinel, C.; Mallart, S.; Juge, S.; Thorimbert, S.; Laffitte, J. A. Tetrahedron: Asymmetry 1991, 2, 555-567.
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(1991)
Tetrahedron: Asymmetry
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Genêt, J.P.1
Pinel, C.2
Mallart, S.3
Juge, S.4
Thorimbert, S.5
Laffitte, J.A.6
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0028343856
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(b) Genêt, J. P.; Pinel, C.; Ratovelomanana-Vidal, V.; Mallart, S.; Pfister, X.; Andrade, M. C. C. D.; Laffitte, J. A. Tetrahedron: Asymmetry 1994, 5, 665-674.
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Tetrahedron: Asymmetry
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Genêt, J.P.1
Pinel, C.2
Ratovelomanana-Vidal, V.3
Mallart, S.4
Pfister, X.5
Andrade, M.C.C.D.6
Laffitte, J.A.7
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See Supporting Information for details
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See Supporting Information for details.
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38349136532
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1H NMR). No enamide 3a was detected. The observation suggests that the conversion of enamide 3a into 2a will be much faster than the first hydrogenation of 1a because 3a lacks aromaticity.
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1H NMR). No enamide 3a was detected. The observation suggests that the conversion of enamide 3a into 2a will be much faster than the first hydrogenation of 1a because 3a lacks aromaticity.
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