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| SHORTPAPER | Synthesis 2006: 1937-1939 DOI: 10.1055/s-2006-942376 |
© Georg Thieme Verlag Stuttgart · New York
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Strecker Reaction of Aldimines Catalyzed by a Nucleophilic N-Heterocyclic Carbene
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| Yoshimasa Fukuda, Yuka Maeda, Kazuhiro Kondo*, Toyohiko Aoyama* |
Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya 467-8603, Japan Fax: +81(52)8363439; e-Mail: kazuk@phar.nagoya-cu.ac.jp; e-Mail: aoyama@phar.nagoya-cu.ac.jp;
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Received
15 December 2005 |
Abstract
The first method for Strecker reaction (cyanation of imines) of aldimines with TMSCN in the presence of N-heterocyclic carbene prepared from 1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride and t-BuOK, as a nucleophilic catalyst, is described. Key words
Strecker reaction - aldimine - N-heterocyclic carbene - imidazolium salt - cyanation
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