Search results for "oxidative cyclization"

showing 3 items of 13 documents

ChemInform Abstract: Oxidative Cyclization of Some Aldehyde Semicarbazones Induced by Metallic Salts.

2010

The oxidative cyclization of some aldehyde semicarbazones 10 with four different oxidizing agents has been effected. The structure of the semicarbazones and the nature of cyclizing agent affected the rate and yield of cyclization but they did not show any influence on the regiochemistry of reaction. In fact, 1,2,4-triazoline 20 was the only heterocyclic ring obtained by the cyclization reaction.

chemistry.chemical_classificationOxidative cyclizationRegioselectivityGeneral MedicineRing (chemistry)AldehydeMetalchemistryvisual_artYield (chemistry)Polymer chemistryOxidizing agentTriazole derivativesvisual_art.visual_art_mediumOrganic chemistryChemInform
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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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A competitive reactivity study on the oxidative cyclization of thiosemicarbazones into 1,3,4-thiadiazoles

2022

Abstract In order to obtain useful insights on the mechanism of formation of 2(3H)-imino-1,3,4-thiadiazoles by oxidative cyclization of aldehyde thiosemicarbazones with Cu(II) or Fe(III) salts, a competitive reactivity study was performed on a suitable set of diversely substituted substrates, by means of HPLC techniques. This approach enabled to exploit Hammett’s equation without performing otherwise difficult-to-run kinetic experiments. The results presented herein support the hypothesis that the formation of the thiadiazole ring is induced by the attack of the oxidizing Lewis acid metal cation onto the imine-like nitrogen atom of the thiosemicarbazone substrate. Beyond mechanistic interpr…

thiosemicarbazonesOrganic ChemistrySettore CHIM/06 - Chimica OrganicaCopper(II) chlorideoxidative cyclization134-thiadiazoleArkivoc
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