Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/9154
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dc.contributor.authorStathopoulos, P.en
dc.contributor.authorPapas, S.en
dc.contributor.authorPappas, C.en
dc.contributor.authorMousis, V.en
dc.contributor.authorSayyad, N.en
dc.contributor.authorTheodorou, V.en
dc.contributor.authorTzakos, A. G.en
dc.contributor.authorTsikaris, V.en
dc.date.accessioned2015-11-24T16:47:14Z-
dc.date.available2015-11-24T16:47:14Z-
dc.identifier.issn1438-2199-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9154-
dc.rightsDefault Licence-
dc.subjectAlkylationen
dc.subjectAmino Acid Sequenceen
dc.subjectAmino Acids/chemistryen
dc.subjectChromatography, High Pressure Liquiden
dc.subjectCysteine/*chemistryen
dc.subjectFluorenes/chemistryen
dc.subjectMolecular Structureen
dc.subjectOligopeptides/*chemical synthesis/chemistry/isolation & purificationen
dc.subjectSolid-Phase Synthesis Techniquesen
dc.subjectSpectrometry, Mass, Electrospray Ionizationen
dc.titleSide reactions in the SPPS of Cys-containing peptidesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1007/s00726-013-1471-7-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/23459989-
heal.identifier.secondaryhttp://download.springer.com/static/pdf/450/art%253A10.1007%252Fs00726-013-1471-7.pdf?auth66=1383208755_e3e97b30f7effffdf03851390978701e&ext=.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2013-
heal.abstractAlkylation of sensitive amino acids during synthesis of biologically important peptides is a common and well-documented problem in Fmoc-based strategy. Herein, we probed for the first time an unexpected S-alkylation of Cys-containing peptides that occur during the final TFA cleavage of peptides from the Wang solid support. Through a battery of approaches (NMR, UV and LC-MS) the formed by-product was assigned as the alkylation of the cysteine sulfydryl group by the p-hydroxyl benzyl group derived from the acidic Wang linker decomposition. Factors affecting this side reaction were monitored and a protocol that minimizes the presence of the by-product is reported.en
heal.publisherSpringer-Verlagen
heal.journalNameAmino Acidsen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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