Results 61 to 70 of about 3,167 (267)
Novel Dihydropyrimidinones: Molecular Docking, Synthesis and Anti-Neoplastic Activity
Recent years have showed great interest in the synthesis of pyrimidinone and its applications in medicinal chemistry. Chalcones were synthesized through the Claisen-Schmidt condensation reaction between substituted aldehydes and acetone in the presence ...
M. P. Toraskar, R. Chaure, S. Sontakke
semanticscholar +1 more source
Comparison of Catalytic Effect of Alkali and Alkaline Earth Metals Hydrogen Sulfate: As the Promoter for an Efficient Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones under Solvent-Free Conditions [PDF]
Alkali and alkaline earth metals hydrogen sulfate catalyzed the one-pot three component condensation reactions of aldehydes, 1,3-dicarbonyl compounds and urea or thiourea under solvent-free conditions leading to 3,4-dihydropyrimidin-2(1H)-ones in high ...
Ahmad Shaabani +4 more
doaj
The catalytic ability of ZrO2/SO42- to promote solventless three-componentcondensation reactions of a diversity of aromatic aldehydes, urea or thoiurea and ethylacetoacetate was studied.
Guillermo Negrón-Silva +4 more
doaj +1 more source
The synthesis of 3,4-dihydropyrimidine-2-ones has been the focus of much interest since they exhibited various biological activities with pharmacology potentials (antibacterial, antitumor, antiviral, and anti-inflammatory).
A. Fadlan +4 more
semanticscholar +1 more source
The most important heterocyclic complexes involved in the manufacture of DNA and RNA are dihydropyrimidines. Through multi-component synthetic procedures like the Biginelli reaction and the Hantzsch dihydropyridine reaction, they were created.
Saba Beigh +6 more
semanticscholar +1 more source
Biological Activity and Efficient Synthesis of 3, 4- Dihydropyrimidin-2-(1H)-one/thione Derivatives [PDF]
The present study aimed to use a method for the synthesis of some 3, 4- dihydropyrimidin-2-(1H) - ones/thiones. The study tried to answer the question whether this reaction can be performed without solvent and with new catalyst or not.
Hatamjafari, Farhad
core +1 more source
Synthesis and Antioxidant Activity of Novel Biginelli Adducts with Phenolic Fragments
In this work, eco-friendly ceric ammonium nitrate (CAN) and ferric chloride hexahydrate catalysts in ethanol/acetonitrile systems were used to efficiently synthesize novel dihydropyrimidinone (-thione) derivatives via the Biginelli reaction. The obtained
Olga V. Snastina +3 more
doaj +1 more source
A mild and efficient catalytic method for synthesis of 5-alkoxycarbonyl-4-aryl-3,4- dihydropyrimidin-2(1H)-ones using KSF montmorillonite as catalyst is described.
Ziyi Zhang +3 more
doaj +1 more source
Synthesis of pyrimidines, aromatic and heteroaromatic acids as Biginelli reaction catalysts [PDF]
Aromatic as well as heteroaromatic acids were found to beexcellent catalysts for the Biginelli three component synthesisof dihydropyrimidinones. Benzoic acid, substituted benzoic acids, five- and six- membered heterocyclic acids can be used for this ...
Adnan, Muhammad +9 more
core
EFFICIENT SODIUM SELENATE-CATALYZED SYNTHESIS OF 3,4-DIHYDRO-2(1H)-PYRIMIDINONES AND –THIONES UNDER SOLVENT-FREE CONDITIONS [PDF]
Sodium selenate efficiently catalyzes the three-component Biginelli reaction of an aldehyde, a,β-keto ester and urea or thiourea under solvent-free conditions to afford the corresponding 3,4-dihydropyrimidin-2(1H)-ones or –thiones in excellent ...
Baghernejad, Bita +3 more
core +2 more sources

