Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/9794
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dc.contributor.authorTheodorou, V.en
dc.contributor.authorKarkatsoulis, A.en
dc.contributor.authorKinigopoulou, M.en
dc.contributor.authorRagoussis, V.en
dc.contributor.authorSkobridis, K.en
dc.date.accessioned2015-11-24T16:51:51Z-
dc.date.available2015-11-24T16:51:51Z-
dc.identifier.issn1424-6376-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9794-
dc.rightsDefault Licence-
dc.subjecttritylamineen
dc.subjecttritylamidesen
dc.subjectammonia synthetic equivalenten
dc.subjectsynthesis of primary amidesen
dc.subjectdetritylationen
dc.subjectpalladium-catalyzed carbonylationen
dc.subjectbase-induced rearrangementen
dc.subjectprotected amino-acidsen
dc.subjectpeptide-synthesisen
dc.subjectorganic-synthesisen
dc.subjectcarboxylic-acidsen
dc.subjectfacile synthesisen
dc.subjectaqueous-mediaen
dc.subjectestersen
dc.subjecttriphenylmethylamineen
dc.titleTritylamine as an ammonia synthetic equivalent: preparation of primary amidesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondary<Go to ISI>://000271148800025-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2009-
heal.abstractA new synthetic route to primary amides via N-tritylamides was developed. The initially formed N-tritylamides, derived from acylation of tritylamine by activated carboxylic acid derivatives, were deprotected with trifluoroacetic acid at room temperature to the desired primary amides in good yields.en
heal.journalNameArkivocen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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