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American Chemical Society, Organic Letters, 4(8), p. 741-744, 2006

DOI: 10.1021/ol053001a

Wiley-VCH Verlag, ChemInform, 26(37), 2006

DOI: 10.1002/chin.200626069

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Hydrogen Bond Catalyzed Direct Reductive Amination of Ketones

Journal article published in 2006 by Dirk Menche, Jorma Hassfeld, Jun Li, Gerd Menche, Antje Ritter, Sven Rudolph
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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Abstract

[reaction: see text] A novel, biomimetic concept for the direct reductive amination of ketones is described that relies on selective imine activation by hydrogen bond formation. The mild, acid- and metal-free process requires only catalytic amounts of thiourea as hydrogen bond donor and utilizes the Hantzsch ester for transfer hydrogenation. The method allows the efficient synthesis of structurally diverse amines.