Search results for "4-Triazoles"

showing 3 items of 3 documents

Fluorinated Heterocyclic Compounds. A Photochemical Approach to a Synthesis of Polyfluoroaryl-1,2,4-triazoles.

2005

The reaction of some fluorinated 1,2,4-oxadiazoles in the presence of methylamine or propylamine has been investigated. The irradiation in methanol or acetonitrile leads with acceptable yields to the corresponding fluorinated 1- methyl- or 1-propyl-1,2,4-triazole.

PharmacologyFLUORO HETEROCYCLESMethylamineOrganic ChemistryQUINAZOLIN-4-ONES124-Triazole124-OXADIAZOLESPropylamineSettore CHIM/06 - Chimica OrganicaGeneral MedicineEXPEDIENT ROUTEPhotochemistryMedicinal chemistryAnalytical Chemistrychemistry.chemical_compound124-TRIAZOLESchemistryTriazole derivativesOrganic chemistry5-MEMBERED HETEROCYCLESIrradiationMethanolAcetonitrilePHOTOINDUCED MOLECULAR-REARRANGEMENTSChemInform
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Insight into non-nucleoside triazole-based systems as viral polymerases inhibitors

2023

Viruses have been recognized as the etiological agents responsible for many pathological conditions ranging from asymptomatic infections to serious diseases, even leading to death. For this reason, many efforts have been made to identify selective viral targets with the aim of developing efficient therapeutic strategies, devoid of drug-resistance issues. Considering their crucial role in the viral life cycle, polymerases are very attractive targets. Among the classes of compounds explored as viral polymerases inhibitors, here we present an overview of non-nucleoside triazole-based compounds identified in the last fifteen years. Furthermore, the structure-activity relationships (SAR) of the …

PharmacologyOrganic ChemistryDrug Discovery123-TriazolesNon-nucleosides antiviral agentsViral polymerasesGeneral MedicineAntiviral therapy124-TriazolesEuropean Journal of Medicinal Chemistry
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Oxidative cyclization of aldehyde thiosemicarbazones induced by potassium ferricyanide and by tris(p-bromophenyl)amino hexachloroantimoniate. A joint…

2005

The oxidative ring closure reaction of some aryl-substituted thiosemicarbazones induced by "bona fide" one-electron abstracting agents was investigated, by means of both experimental and computational techniques. The corresponding 1,2,4-triazole derivatives were the only cyclization products observed. The occurrence of two slightly different mechanistic pathways for the reaction is discussed.

chemistry.chemical_classificationTrisOxidative cyclizationOrganic ChemistryOxidative cyclization thiosemicarbazones 124-triazolesOxidative phosphorylationSettore CHIM/06 - Chimica OrganicaRing (chemistry)AldehydeMedicinal chemistrylcsh:QD241-441Potassium ferricyanidechemistry.chemical_compoundlcsh:Organic chemistrychemistryOrganic chemistry
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