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dc.contributor.authorOUAHRANI MOHAMMED RIDHA-
dc.contributor.authorSEGNI LADJEL-
dc.contributor.authorDENDOUGUI HOUCINE-
dc.date.accessioned2006-
dc.date.available2006-
dc.date.issued2006-
dc.identifier.issn2170-0672-
dc.identifier.urihttp://dspace.univ-ouargla.dz/jspui/handle/123456789/6521-
dc.descriptionAST Annales des Sciences et Technologieen_US
dc.description.abstractThe stechiometry of the paratoluene sulphonic acid is a determining factor of the reaction of cyclization of the oxindolic methylketone 1. Indeed, the oxindolic methylketone 1 is cyclized in pentacyclic compound 2 in the presence of an adequate quantity of paratoluene sulphonic acid in good yield. Obtaining the tow epimeric indolenines 3a and 3b enabled us to explain the mechanism of this reaction.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesvolume 1 numéro 1 AST 2006;-
dc.subjectCyclizationen_US
dc.subjectindolenineen_US
dc.subjectmacidic mediuen_US
dc.subjectmethylketone oxindolesen_US
dc.titleSTUDY OF THE MECHANISM OF CYCLIZATION AND DECOMPOSITION OF METHYLKETONES OXINDOLES IN ACIDIC MEDIUMen_US
dc.typeArticleen_US
Appears in Collections:volume 1 numéro 1 AST 2006

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