Results 101 to 110 of about 611 (196)

Green and Efficient Synthesis of Dihydropyrimidinone Analogues via Hpa-Clay Catalyzed Biginelli Reaction

open access: yesChemistry Journal of Moldova: General, Industrial and Ecological Chemistry
This study introduces an environmentally sustainable approach for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones (DHPMs), via the Biginelli reaction. A heterogeneous catalyst, Heteropolyacid-Clay (HPA-Clay), is developed by immobilizing H5PV2W10O40 on ...
Nuzhat Rehman   +6 more
doaj   +1 more source

Exploring the binding dynamics of anticancer Dihydropyrimidinone derivatives with Serum Albumin: A multispectral approach

open access: yesChemical Physics Impact
In this work, we have investigated the synthesis and characterization of two novel anticancer agents, 5-acetyl-6-methyl-4-phenyl-3,4-dihydropyrimidin-2(1H)-one (L1) and 2-Acetyl-4-(3,4-dimethoxy-phenyl)-6-methyl-3,4-dihydro-1H-pyrimidin-2-one (L2 ...
Chandraprakash Gond   +5 more
doaj   +1 more source

Sustainable Biginelli chemistry: Indian contributions to green multicomponent synthesis

open access: yesDiscover Chemistry
The Biginelli Reaction is a one-pot acid-catalysed cyclo-condensation procedure that combines urea, β-ketoester, and aromatic aldehydes to create functionalised DHPMs. For more than a century, this three-component reaction has been recognised as a method
Rajni   +4 more
doaj   +1 more source

Synthesis of 3,4-Dihydropyrimidin-2(1H)-one-5-carboxamides [PDF]

open access: yes, 2010
The synthesis of various dihydropyrimidinone derivatives bearing carbamoyl moieties in 5-position under reflux conditions and microwave irradiation is described.
Mousa Soleymani, Hamid Reza Memarian
core  

Hybrid Dihydropyrimidinones Targeting AKT Signaling: Antitumor Activity in Hormone-Dependent 2D and 3D Cancer Models. [PDF]

open access: yesPharmaceutics
Tejada AH   +11 more
europepmc   +1 more source

Design, synthesis and evaluation of fluorescent dihydropyridine-dihydropyrimidinone hybrids as inducers of cell-cycle arrest in a prostate cancer cell line <i>via</i> Aurora kinase interactions. [PDF]

open access: yesRSC Med Chem
de Souza VP   +12 more
europepmc   +1 more source

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