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The decarboxylative Blaise reaction. | LitMetric

The decarboxylative Blaise reaction.

J Org Chem

Chemical Development Division, LG Life Sciences, Ltd./R&D, 104-1 Moonji-dong, Yusong-gu, Daejeon 305-380, Korea.

Published: December 2007

Reaction of aryl nitriles with potassium ethyl malonate in the presence of zinc chloride and a catalytic amount of Hünig's base provided beta-amino acrylates in moderate to good yield. Compared to the classical Blaise reaction, this reaction is safer (endothermic), devoid of lacrimatory reagent, and is possible with 0.5-1.0 equiv of zinc chloride.

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Source
http://dx.doi.org/10.1021/jo701743mDOI Listing

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