Abstract
One-pot solvent free three components coupling of aryl aldehydes, β-dicarbonyl compounds, urea or thiourea was performed to afford corresponding 3,4-dihydropyrimidine-2-ones and their sulfur analogs 3,4-dihydro-pyrimidine-2-thiones. It is the first report of BF3.ACN catalyzed the solvent-free synthesis of pyrimidone analogs.
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APA
Kharpe, A. A., Choudhare, T. S., Mokale, S. N., & Netankar, P. D. (2019). One pot BF3.MeCN catalyzed solvent free synthesis of 3,4-dihydropyrimidine-2-one analogues. European Chemical Bulletin, 8(6), 176–179. https://doi.org/10.17628/ecb.2019.8.176-179
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