5-(1-(4-Hydroxy-6-methyl-2-oxo-2<i>H</i>-pyran-3-yl)-2-oxo-2-phenylethyl)-1,3-dimethylpyrimidine-2,4,6(1<i>H</i>,3<i>H</i>,5<i>H</i>)-trione

5-(1-(4-Hydroxy-6-methyl-2-oxo-2<i>H</i>-pyran-3-yl)-2-oxo-2-phenylethyl)-1,3-dimethylpyrimidine-2,4,6(1<i>H</i>,3<i>H</i>,5<i>H</i>)-trione

Multicomponent reactions have been demonstrated as a promising tool for the creation of diverse molecular structures with enhanced efficiency, reduced waste, and a high atom economy. Arylglyoxal monohydrates with two different carbonyl groups are well known as worthwhile synthons in organic synthesi...

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Bibliographic Details
Main Authors: Yuliya E. Ryzhkova, Varvara M. Kalashnikova, Fedor V. Ryzhkov, Michail N. Elinson
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Molbank
Subjects:
multicomponent reaction
tandem Knoevenagel–Michael process
phenylglyoxal hydrate
1,3-dimethylbarbituric acid
4-hydroxy-6-methyl-2<i>H</i>-pyran-2-one
((2<i>H</i>-pyran-3-yl)-2-oxo-2-phenylethyl)-1,3-dimethylpyrimidine
Online Access:https://www.mdpi.com/1422-8599/2023/2/M1640

Internet

https://www.mdpi.com/1422-8599/2023/2/M1640

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