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  5. Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ
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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/9453
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dc.contributor.authorTheodorou, V.en
dc.contributor.authorGogou, M.en
dc.contributor.authorPhilippidou, M.en
dc.contributor.authorRagoussis, V.en
dc.contributor.authorParaskevopoulos, G.en
dc.contributor.authorSkobridis, K.en
dc.date.accessioned2015-11-24T16:49:15Z-
dc.date.available2015-11-24T16:49:15Z-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9453-
dc.rightsDefault Licence-
dc.subjectbeta,gamma-unsaturated n-tritylamidesen
dc.subjectbeta,gamma-unsaturated primary amidesen
dc.subject3-alkenamidesen
dc.subjectisomerizationen
dc.subjectdetritylationen
dc.subjectbase-induced rearrangementen
dc.subjectunsaturated amidesen
dc.subjectstereoselective synthesesen
dc.subjectdelta-lactamsen
dc.subjectgamma-lactamsen
dc.subjectpalladiumen
dc.subjectestersen
dc.subject3-alkenamidesen
dc.subjecttritylamineen
dc.subject4-alkenyl-2-azetidinonesen
dc.titleSynthesis of beta,gamma-unsaturated primary amides from alpha,beta-unsaturated acids and investigation of the mechanismen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1016/j.tet.2011.05.096-
heal.identifier.secondary<Go to ISI>://000293109400015-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0040402011007861/1-s2.0-S0040402011007861-main.pdf?_tid=c701e476-3a30-11e3-95c8-00000aacb35d&acdnat=1382346872_6eb56bad3417bf94a538dcadb85b8af6-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2011-
heal.abstractalpha,beta-Unsaturated acids, through their acid chlorides, react with tritylamine in the presence of triethylamine under mild conditions, to afford in high yield and high regioselectivity the corresponding beta,gamma-unsaturated tritylamides. Detritylation with TFA generates quantitatively beta,gamma-unsaturated primary amides. An investigation of this deconjugative isomerization was performed. (C) 2011 Elsevier Ltd. All rights reserved.en
heal.publisherElsevieren
heal.journalNameTetrahedronen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
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