An efficient and practical method is developed for the diversity-oriented synthesis of β-enaminones via three-component reaction between substituted β-nitrostyrenes, β-dicarbonyl compounds and amines for the generation of a wide range of structurally interesting and pharmacologically significant compounds under mild conditions.
W. Ye, Y. Li, L. Zhou, J. Liu and C. Wang, Green Chem., 2015, 17, 188 DOI: 10.1039/C4GC01234H
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