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DC Field | Value | Language |
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dc.contributor.author | OUAHRANI MOHAMMED RIDHA | - |
dc.contributor.author | SEGNI LADJEL | - |
dc.contributor.author | DENDOUGUI HOUCINE | - |
dc.date.accessioned | 2006 | - |
dc.date.available | 2006 | - |
dc.date.issued | 2006 | - |
dc.identifier.issn | 2170-0672 | - |
dc.identifier.uri | http://dspace.univ-ouargla.dz/jspui/handle/123456789/6521 | - |
dc.description | AST Annales des Sciences et Technologie | en_US |
dc.description.abstract | The 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.iso | en | en_US |
dc.relation.ispartofseries | volume 1 numéro 1 AST 2006; | - |
dc.subject | Cyclization | en_US |
dc.subject | indolenine | en_US |
dc.subject | macidic mediu | en_US |
dc.subject | methylketone oxindoles | en_US |
dc.title | STUDY OF THE MECHANISM OF CYCLIZATION AND DECOMPOSITION OF METHYLKETONES OXINDOLES IN ACIDIC MEDIUM | en_US |
dc.type | Article | en_US |
Appears in Collections: | volume 1 numéro 1 AST 2006 |
Files in This Item:
File | Description | Size | Format | |
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A010109.pdf | 265,02 kB | Adobe PDF | View/Open |
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