Thiourea-Catalyzed Direct Reductive Amination of Aldehydes
Dirk Menche*, Fatih Arikan
*Gesellschaft für Biotechnologische Forschung mbH, Medzinische Chemie, Mascheroder Weg 1, D-38124 Braunschweig, Germany, Email: dme05gbf.de
D. Menche, F. Arikan, Synlett, 2006, 841-844.
DOI: 10.1055/s-2006-939052
Abstract
A hydrogen-bond-catalyzed, acid- and metal-free direct reductive amination of aldehydes uses thiourea as organocatalyst and the Hantzsch ester for transfer-hydrogenation. This methods allows for the high-yielding synthesis of diverse amines.
see article for more examples
While ads financed 62% of the published abstracts in 2024, donations allowed us to publish additional 12%. 26% of the abstracts have been published voluntarly. If you kindly donate, we can publish more freely accessible information and help the chemical community even more:
If you don't like pawalls or a flood of more and more advertising, then you can send a clear signal here!
Hydrogen Bond Catalyzed Direct Reductive Amination of Ketones
D. Menche, J. Hassfeld, J. Li, G. Menche, A. Ritter, S. Rudolph, Org. Lett., 2006, 8, 741-744.
Key Words
amines, reductive amination, organocatalysis, hydrogen bonds, Hantzsch ester
ID: J60-Y2006-4340