Please use this identifier to cite or link to this item:
https://olympias.lib.uoi.gr/jspui/handle/123456789/8237
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DC Field | Value | Language |
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dc.contributor.author | V. Theodorou, | en |
dc.contributor.author | M. Gogou, | en |
dc.contributor.author | A. Giannousi, | en |
dc.contributor.author | K. Skobridis | en |
dc.date.accessioned | 2015-11-24T16:40:09Z | - |
dc.date.available | 2015-11-24T16:40:09Z | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/8237 | - |
dc.rights | Default Licence | - |
dc.subject | N,N-Diacylation, N-monoacylation, 2-aminopyrimidine, aminopyrazine, deactivated anilines, Imatinib analogues | en |
dc.title | Insights into the N,N-diacylation reaction of 2-aminopyrimidines and deactivated anilines: an alternative N-monoacylation reaction | en |
heal.type | journalArticle | - |
heal.type.en | Journal article | en |
heal.type.el | Άρθρο Περιοδικού | el |
heal.identifier.secondary | http://quod.lib.umich.edu/a/ark/5550190.p008.209/1 | - |
heal.language | en | - |
heal.access | campus | - |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
heal.publicationDate | 2013 | - |
heal.abstract | During 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.journalName | Arkivoc (Archive for Organic Chemistry) | en |
heal.journalType | peer reviewed | - |
heal.fullTextAvailability | TRUE | - |
Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ |
Files in This Item:
File | Description | Size | Format | |
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Skobridis-2013-Insights into the.pdf | 361.77 kB | Adobe PDF | View/Open |
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