Volume 49, Issue 44 p. 8048
Inside Cover
Free Access

Inside Cover: Enantioselective Synthesis of Amines: General, Efficient Iron-Catalyzed Asymmetric Transfer Hydrogenation of Imines (Angew. Chem. Int. Ed. 44/2010)

Shaolin Zhou

Shaolin Zhou

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock (Germany), Fax: (+49) 381-1281-51113 http://www.catalysis.de

Search for more papers by this author
Steffen Fleischer

Steffen Fleischer

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock (Germany), Fax: (+49) 381-1281-51113 http://www.catalysis.de

Search for more papers by this author
Dr. Kathrin Junge

Dr. Kathrin Junge

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock (Germany), Fax: (+49) 381-1281-51113 http://www.catalysis.de

Search for more papers by this author
Shoubhik Das

Shoubhik Das

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock (Germany), Fax: (+49) 381-1281-51113 http://www.catalysis.de

Search for more papers by this author
Daniele Addis

Daniele Addis

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock (Germany), Fax: (+49) 381-1281-51113 http://www.catalysis.de

Search for more papers by this author
Prof. Dr. Matthias Beller

Prof. Dr. Matthias Beller

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock (Germany), Fax: (+49) 381-1281-51113 http://www.catalysis.de

Search for more papers by this author
First published: 03 August 2010
Citations: 1

Graphical Abstract

Although iron is one of the most abundant metals, its application to catalysis is still in its infancy. In their Communication on page 8121 ff., M. Beller and co-workers present the first iron-catalyzed asymmetric transfer hydrogenation of imines. Iron carbonyl complexes in the presence of a tetradentate P2N2 ligand catalyze the reduction of N-diphenylphosphinylimines with high enantioselectivity (99 %) and good yields (98 %).

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.