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Synfacts 2006(10): 1034-1034
DOI: 10.1055/s-2006-949341
DOI: 10.1055/s-2006-949341
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York
Asymmetric Reductive Amination: Access to Chiral Primary Amines
T. C. Nugent*, A. K. Ghosh, V. N. Wakchaure, R. R. Mohanty
International University Bremen, Germany
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
21. September 2006 (online)
![](https://www.thieme-connect.de/media/synfacts/200610/lookinside/thumbnails/10.1055-s-2006-949341-1.jpg)
Significance
This is a very nice extension of the previous work by this group in elaborating the scope of ketones used in the reductive amination. The importance of the heterogeneous hydrogenation catalyst was also shown as well as the significance of solvent, temperature and molarity. Shown above is a very interesting finding about the heterogeneous catalyst conditions and the classification of suitable substrates for the three catalyst systems tested.