A convenient and improved procedure for the cyanation of enamines and 1,3-dicarboxyl compounds

Article abstract of DOI:10.1080/00397919408010246

The direct cyanation of enamines 2a-f using acylsubstituted cyanatobenzenes 1a-c and cyanatoanthraquinone 1d furnishes β-cyanoenamines 3a-f which upon hydrolysis afford the cyanoketones 4a,b. 2-Cyano-1,3-diketones 6a-c are obtained starting from compounds

Full text of DOI:10.1080/00397919408010246

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Synthetic Communications: An
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Organic Chemistry
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A Convenient and Improved
Procedure for the Cyanation of
Enamines and 1,3-Dicarbonyl
Compounds
K. Buttke a & H.-J. Niclas a
a Institute for Applied Chemistry Berlin-Adlershof ,
Rudower Chaussee 5, 12484, Berlin, Germany
Published online: 23 Sep 2006.
To cite this article: K. Buttke & H.-J. Niclas (1994) A Convenient and Improved
Procedure for the Cyanation of Enamines and 1,3-Dicarbonyl Compounds, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 24:22, 3241-3248, DOI: 10.1080/00397919408010246
To link to this article: http://dx.doi.org/10.1080/00397919408010246
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