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Synthesis 2012; 44(13): 1977-1982
DOI: 10.1055/s-0031-1291125
DOI: 10.1055/s-0031-1291125
paper
S-Benzyl Isothiouronium Chloride as a Recoverable Organocatalyst for the Direct Reductive Amination of Ketones with Hantzsch Ester
Further Information
Publication History
Received: 05 March 2012
Accepted after revision: 17 April 2012
Publication Date:
25 May 2012 (online)
Abstract
The direct reductive amination of ketones using the Hantzsch ester in the presence of S-benzyl isothiouronium chloride as a recoverable organocatalyst is reported. A wide range of ketones as well as amines were found to give the expected products in moderate to excellent yields.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
-
References
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For the reduction of ketimines, see:
For the direct reductive amination of ketones, see:
For studies on the hydrogen bond in isothiouronium compounds, see: