Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377721 | Bioorganic & Medicinal Chemistry Letters | 2006 | 4 Pages |
Abstract
A simple and efficient method for the synthesis of N3-substituted 3,4-dihydropyrimidinones by aza-Michael addition reactions of 3,4-dihydropyrimidinones to α,β-ethylenic compounds catalyzed by KF/Al2O3 is described. The advantage of this method is high regioselectivity, high purity, and the use of a cheaper, milder, and efficient catalyst for the hetero-Michael addition reaction.
Graphical abstractA simple and efficient method for the synthesis of N3-substituted 3,4-dihydropyrimidinones by aza-Michael addition reactions of 3,4-dihydropyrimidinones to α,β-ethylenic compounds catalyzed by KF/Al2O3 is described.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xicun Wang, Zhengjun Quan, Jun-Ke Wang, Zhang Zhang, Mangang Wang,