Results 81 to 90 of about 2,914 (164)

Synthesis and biological evaluation of 2-methoxy- and 2-Methylthio-6-[(2′-alkylamino)ethyl]-4(3H)-pyrimidinones with anti-rubella virus activity

open access: yes, 1999
The synthesis of a new family of antiviral compounds, 2-methoxy-, and 2-methylthio-6-[(2'-alkylamino)ethyl]-4(3H)-pyrimidinones, has been accomplished.
CONTI CINZIA   +6 more
core   +1 more source

Solvent-free and green synthesis of fused pyrimidine derivatives catalyzed by pillar[5]arene-based Lewis acid ionic liquid

open access: yesScientific Reports
This study presents a solvent-free and green approach for the synthesis of novel 7,9-diaryl-6H,7H-chromeno[4,3-d]thiazolo[3,2-a]pyrimidin-6-one (DCTP) derivatives using a newly developed pillar[5] arene-based Lewis acid ionic liquid (P5/Py[CuBr2]Br) as ...
Soheila Rastegar   +5 more
doaj   +1 more source

Pentafluorophenylammonium triflate (PFPAT) catalyzed facile construction of substituted chromeno[2,3-d]pyrimidinone derivatives and their antimicrobial activity

open access: yesJournal of Advanced Research, 2014
A new, simple thermally efficient and solvent-free condensation of 2-amino-3-cyano-6-methyl-4-phenyl-4H-pyran-5-ethylcarboxylate derivatives with coumarin-3-carboxylic acid employing pentafluorophenylammonium triflate (PFPAT) as an inexpensive ...
Majid Ghashang   +2 more
doaj   +1 more source

Introduction of Poly(4-Vinylpyridine) as an Efficient Promotor for the Synthesis of Pyrano[2,3-d]Pyrimidinones and Pyrido[2,3-d]Pyrimidines

open access: yes, 2018
This article describes an efficient method for the synthesis of pyrano[2,3-d]pyrimidinones and pyrido[2,3-d]pyrimidines via promotion of the condensation of aromatic aldehydes, malononitrile and barbituric acid and/or 6-amino-1,3-dimethyluracil in the ...
Farhad Shirini (703231)   +3 more
core   +1 more source

Identification of kinase inhibitors as potential host-directed therapies for intracellular bacteria

open access: yesScientific Reports
The emergence of antimicrobial resistance has created an urgent need for alternative treatments against bacterial pathogens. Here, we investigated kinase inhibitors as potential host-directed therapies (HDTs) against intracellular bacteria, specifically ...
Robin H. G. A. van den Biggelaar   +9 more
doaj   +1 more source

Design and Synthesis of Bicyclic Pyrimidinones as Potent and Orally Bioavailable HIV-1 Integrase Inhibitors

open access: yes, 2016
HIV integrase is one of the three enzymes encoded by HIV genome and is essential for viral replication, but integrase inhibitors as marketed drugs have just very recently started to emerge.
Annalise Di Marco (2338006)   +17 more
core   +1 more source

Design, Synthesis, Antimicrobial Activity, and Molecular Docking of Novel Thiazoles, Pyrazoles, 1,3-Thiazepinones, and 1,2,4-Triazolopyrimidines Derived from Quinoline-Pyrido[2,3-d] Pyrimidinones

open access: yesPharmaceuticals
Background: Recently, pyrido[2,3-d] pyrimidine, triazolopyrimidine, thiazolopyrimidine, quinoline, and pyrazole derivatives have gained attention due to their diverse biological activities, including antimicrobial, antioxidant, antitubercular, antitumor,
Ameen Ali Abu-Hashem, Sami A. Al-Hussain
doaj   +1 more source

‐quinazolin‐4‐ones via Diels–Alder Adducts of Phenyl Vinyl Sulfone to Cyclobutene‐Annelated Pyrimidinones

open access: yes, 2006
Under basic conditions (Et3N, dioxane), the aromatic amidines 4 and also S-methylisothiourea 4g cleanly undergo Michael addition to methyl 2-chloro-2-cyclopropylideneacelate (5), followed by intramolecular nucleophilic substitution, cyclopropyl to ...
Nizamov, Shamil   +11 more
core   +1 more source

Dérivés de 2(1H)-pyrimidinones et d'isatogènes : synthèse, application de la chimie clic et activités biologiques [PDF]

open access: yes, 2011
La synthèse de 1,2,3-triazoles disubstitués originaux via la cycloaddition 1,3-dipolaire catalysée par le cuivre(I) entre un alcyne et un azoture (CuAAC), en utilisant les dérivés éthynyles de la 2(1H)-pyrimidinone, les dérivés azides de la 2(1H ...
Najahi, Ennaji
core  

Asymmetric Carbon−Carbon Bond Formations in Conjugate Additions of Lithiated N-Boc Allylic and Benzylic Amines to Nitroalkenes:  Enantioselective Synthesis of Substituted Piperidines, Pyrrolidines, and Pyrimidinones

open access: yes, 2016
(−)-Sparteine mediated lithiations of N-Boc-allylic and benzylic amines provide configurationally stable intermediates which on conjugate additions to nitroalkenes provide highly enantioenriched enecarbamate products in good yields, and with high ...
Timothy A. Johnson (2384710)   +4 more
core   +1 more source

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