Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/8237
Full metadata record
DC FieldValueLanguage
dc.contributor.authorV. Theodorou,en
dc.contributor.authorM. Gogou,en
dc.contributor.authorA. Giannousi,en
dc.contributor.authorK. Skobridisen
dc.date.accessioned2015-11-24T16:40:09Z-
dc.date.available2015-11-24T16:40:09Z-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8237-
dc.rightsDefault Licence-
dc.subjectN,N-Diacylation, N-monoacylation, 2-aminopyrimidine, aminopyrazine, deactivated anilines, Imatinib analoguesen
dc.titleInsights into the N,N-diacylation reaction of 2-aminopyrimidines and deactivated anilines: an alternative N-monoacylation reactionen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://quod.lib.umich.edu/a/ark/5550190.p008.209/1-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2013-
heal.abstractDuring the N-benzoylation reaction for the synthesis of N-substituted aminopyrimidines, an undesired N,N-diacylation reaction took place. The extension of this N-acylation reaction to a series of several 2-aminopyrimidines, aminopyrazines and highly deactivated anilines produced analogous results. The possible mechanism responsible for that behavior is investigated and an advantageous alternative procedure for the clean formation of the desired amides is suggested.en
heal.journalNameArkivoc (Archive for Organic Chemistry)en
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

Files in This Item:
File Description SizeFormat 
Skobridis-2013-Insights into the.pdf361.77 kBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons