Results 101 to 110 of about 2,041,750 (198)
The results showed that the (NGAL) in female patients increased to (230.52 ± 42.25 pg/mL) compared to healthy patients, which was (188.01 ± 33.20 pg/mL), with a statistically significant difference at a probability level of P ≤ 0.05. A ROC curve analysis
Mohammed Mahal, Osama Ibrahim
doaj +1 more source
P(HEMA)-SO₃H catalyzed Biginelli reaction
Dihidropirimidinonlar (DHPM)'ler farmasötik ve medikal kimyada çok önemli bileşiklerdir. Dihidropirimidinonların sentezi için en yaygın kullanılan yöntem, Biginelli reaksiyonu olarak bilinen, etil asetoasetat, aril aldehit ve üre (veya tiyoüre)’ nin ...
Berthe, Mamadou Lamine
core
Several chiral phosphoric acids were evaluated as organocatalysts for the enantioselective Biginelli reaction of aliphatic aldehydes. With a chiral phosphoric acid derived from 3,3′-bis(3,5-di-tert-butyl-4-methoxyphenyl)-1,1′-binaphthalene-2,2′-diol, and
Zhenhua Gao +8 more
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The Biginelli reaction synthesizes dihydropyrimidones through a multi-component reaction. A β-ketoester, aldehyde, and urea or thiourea react in the presence of an acid catalyst to form these dihydropyrimidones.
Kumara Swamy Taviti +5 more
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An Environmentally Friendly Solvent-free Synthesis of 3,4-Dihydropyrimidinones using a p-Aminobenzene Sulfonic Acid Catalyzed Biginelli Reaction [PDF]
Anhydrous p-aminobenzene sulphonic acid mediated solvent-free protocol is described for the synthesis of dihydropyrimidinones by the cyclocondensation of aldehydes, β-ketoesters and urea/thiourea.
Wu, MS, Zhang, XZ, He, P
core
Biginelli reaction catalyzed by ‘Ionic liquid- ethylene glycol’ protected copper nanoparticles at room temperaturea.
Subho Mozumdar (141584) +4 more
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Synthesis Of Modified Biginelli Compounds
The Biginelli reaction has been a distinguished reaction for many years. Their products, the Dihydropyrimidones have been shown to contain a vast array of bioactivity especially when they contain other known bioactive functional groups.
Collins, Michelle Sarah
core
: The Biginelli reaction is a multicomponent chemical reaction that synthesises 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) from a β-keto ester, an aryl aldehyde, and urea, as described by Pietro Biginelli in 1891.
Priyanka Sharma, Sourav Handique
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Cobalt Ferrite Nanoparticles: Highly Efficient Catalysts for the Biginelli Reaction
This study introduces an efficient and sustainable catalytic system utilizing cobalt ferrite nanoparticles (CoFe2O4-NPs) for the synthesis of valuable 6-amino-2-oxo-4-phenyl (or 4-chlorophenyl)-1,2,3,4-tetrahydropyrimidine-5-carbonitrile derivatives ...
Emad M. El-Telbani +3 more
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Dihydropyrimidinones and dihydropyrimidine thiones are biologically active compounds that have been of interest in the medicinal field. The most common synthetic route to these molecules is the Biginelli reaction, which involves a multicomponent ...
Lyth, Kyle A., David, Rem Quintin V.
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