Enantioselective Synthesis of Amines: General, Efficient Iron‐Catalyzed Asymmetric Transfer Hydrogenation of Imines

In the iron age: A readily accessible, active iron catalyst serves in the straightforward, catalytic transfer hydrogenation of imines (see scheme). A series of imines are converted into chiral amines in high yields and very good enantioselectivities. This method should find broad application in the...

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Published in:Angewandte Chemie International Edition Vol. 49; no. 44; pp. 8121 - 8125
Main Authors: Zhou, Shaolin, Fleischer, Steffen, Junge, Kathrin, Das, Shoubhik, Addis, Daniele, Beller, Matthias
Format: Journal Article
Language:English
Published: Weinheim Wiley‐VCH Verlag 25.10.2010
WILEY-VCH Verlag
WILEY‐VCH Verlag
Wiley
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ISSN:1433-7851, 1521-3773, 1521-3773
Online Access:Get full text
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Summary:In the iron age: A readily accessible, active iron catalyst serves in the straightforward, catalytic transfer hydrogenation of imines (see scheme). A series of imines are converted into chiral amines in high yields and very good enantioselectivities. This method should find broad application in the search for bioactive chiral amines.
Bibliography:http://dx.doi.org/10.1002/anie.201002456
BMBF
istex:D3A21C3EB756CE6689B455AD84FC1DB22653C4C6
State of Mecklenburg-Western Pomerania
DFG
ark:/67375/WNG-1GS85CND-6
ArticleID:ANIE201002456
This work was funded by the State of Mecklenburg-Western Pomerania, the BMBF, and the DFG (Leibniz prize). We thank Dr. W. Baumann, Dr. C. Fischer, S. Buchholz, S. Schareina, and A. Kammer, A. Koch, S. Rossmeisl, and K. Mevius for their excellent technical and analytical support.
This work was funded by the State of Mecklenburg‐Western Pomerania, the BMBF, and the DFG (Leibniz prize). We thank Dr. W. Baumann, Dr. C. Fischer, S. Buchholz, S. Schareina, and A. Kammer, A. Koch, S. Rossmeisl, and K. Mevius for their excellent technical and analytical support.
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ISSN:1433-7851
1521-3773
1521-3773
DOI:10.1002/anie.201002456