A new hydroxydiphosphine as a ligand for Rh(I)-catalyzed enantioselective hydrogenation

Tetrahedron Asymmetry

Volumn 13, Issue 15, 2002, Pages 1615-1620

  Komarov, Igor V ^a   Monsees, Axel ^b   Kadyrov, Renat ^b   Fischer, Christine ^a   Schmidt, Ute ^a   Börner, Armin ^a  

^a UNIVERSITY OF ROSTOCK   (Germany)

^b EVONIK INDUSTRIES AG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AMINO ACID; BETA AMINO ACID; CAMPHOR DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; HYDROXYL GROUP; LIGAND; PHOSPHINE DERIVATIVE; RHODIUM COMPLEX;

ARTICLE; CATALYSIS; ENANTIOSELECTIVITY; HYDROGENATION; PRECURSOR; PRIORITY JOURNAL; SYNTHESIS;

EID: 0037077793     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(02)00372-5     Document Type: Article

References (23)

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19. For reports on the homogeneously catalyzed enantioselective hydrogenation of β-acylamido dehydroamido acids, see: (a) Achiwa, K.; Soga, T. Tetrahedron Lett. 1978, 1119-1120; (b) Lubell, W. D.; Kitamura, M.; Noyori, R. Tetrahedron: Assymmetry 1991, 2, 543-554; (c) Zhu, G.; Chen, Z.; Zhang, X. J. Org. Chem. 1999, 64, 6907-6910; (d) Heller, D.; Holz, J.; Drexler, H.-J.; Lang, J.; Krimmer, H.-P.; Drauz, K.; Börner, A. J. Org. Chem. 2001, 6816-6817; (e) Zhou, Y.-G.; Tang, W.; Wang, W.-B.; Li, W.; Zhang, X. J. Am. Chem. Soc. 2002, 124, 4952-4953.
20. For reports on the homogeneously catalyzed enantioselective hydrogenation of β-acylamido dehydroamido acids, see: (a) Achiwa, K.; Soga, T. Tetrahedron Lett. 1978, 1119-1120; (b) Lubell, W. D.; Kitamura, M.; Noyori, R. Tetrahedron: Assymmetry 1991, 2, 543-554; (c) Zhu, G.; Chen, Z.; Zhang, X. J. Org. Chem. 1999, 64, 6907-6910; (d) Heller, D.; Holz, J.; Drexler, H.-J.; Lang, J.; Krimmer, H.-P.; Drauz, K.; Börner, A. J. Org. Chem. 2001, 6816-6817; (e) Zhou, Y.-G.; Tang, W.; Wang, W.-B.; Li, W.; Zhang, X. J. Am. Chem. Soc. 2002, 124, 4952-4953.
21. For reports on the homogeneously catalyzed enantioselective hydrogenation of β-acylamido dehydroamido acids, see: (a) Achiwa, K.; Soga, T. Tetrahedron Lett. 1978, 1119-1120; (b) Lubell, W. D.; Kitamura, M.; Noyori, R. Tetrahedron: Assymmetry 1991, 2, 543-554; (c) Zhu, G.; Chen, Z.; Zhang, X. J. Org. Chem. 1999, 64, 6907-6910; (d) Heller, D.; Holz, J.; Drexler, H.-J.; Lang, J.; Krimmer, H.-P.; Drauz, K.; Börner, A. J. Org. Chem. 2001, 6816-6817; (e) Zhou, Y.-G.; Tang, W.; Wang, W.-B.; Li, W.; Zhang, X. J. Am. Chem. Soc. 2002, 124, 4952-4953.
22. For reports on the homogeneously catalyzed enantioselective hydrogenation of β-acylamido dehydroamido acids, see: (a) Achiwa, K.; Soga, T. Tetrahedron Lett. 1978, 1119-1120; (b) Lubell, W. D.; Kitamura, M.; Noyori, R. Tetrahedron: Assymmetry 1991, 2, 543-554; (c) Zhu, G.; Chen, Z.; Zhang, X. J. Org. Chem. 1999, 64, 6907-6910; (d) Heller, D.; Holz, J.; Drexler, H.-J.; Lang, J.; Krimmer, H.-P.; Drauz, K.; Börner, A. J. Org. Chem. 2001, 6816-6817; (e) Zhou, Y.-G.; Tang, W.; Wang, W.-B.; Li, W.; Zhang, X. J. Am. Chem. Soc. 2002, 124, 4952-4953.
23. For reports on the homogeneously catalyzed enantioselective hydrogenation of β-acylamido dehydroamido acids, see: (a) Achiwa, K.; Soga, T. Tetrahedron Lett. 1978, 1119-1120; (b) Lubell, W. D.; Kitamura, M.; Noyori, R. Tetrahedron: Assymmetry 1991, 2, 543-554; (c) Zhu, G.; Chen, Z.; Zhang, X. J. Org. Chem. 1999, 64, 6907-6910; (d) Heller, D.; Holz, J.; Drexler, H.-J.; Lang, J.; Krimmer, H.-P.; Drauz, K.; Börner, A. J. Org. Chem. 2001, 6816-6817; (e) Zhou, Y.-G.; Tang, W.; Wang, W.-B.; Li, W.; Zhang, X. J. Am. Chem. Soc. 2002, 124, 4952-4953.