Abstract
Meldrum's acid catalyzed the reaction of tetracyanoethylene with aromatic, heteroaromatic, and conjugated aldehydes led to arylidenemalononitrile in water in good yields at 80° C. The work-up of reactions is very simple and the crude products are sufficiently pure to be used without further purification. The procedure provides an alternative method for the synthesis of arylidenemalononitrile. © 2008 Pharmaceutical Society of Japan.
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Shaabani, A., Rezayan, A. H., Heidary, M., & Sarvary, A. (2008). Meldrum’s acid catalyzed reaction of tetracyanoethylene and aldehydes in water: A novel approach to arylidenemalononitrile. Chemical and Pharmaceutical Bulletin, 56(10), 1480–1482. https://doi.org/10.1248/cpb.56.1480
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