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dc.contributor.authorElemes, Y.en
dc.contributor.authorRagnarsson, U.en
dc.date.accessioned2015-11-24T16:49:16Z-
dc.date.available2015-11-24T16:49:16Z-
dc.identifier.issn0300-922X-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9456-
dc.rightsDefault Licence-
dc.subjectasymmetric-synthesisen
dc.subjectderivativesen
dc.subjectenantiomersen
dc.subjectseparationen
dc.subjectalkylationen
dc.subjectchiralityen
dc.subjectcomplexesen
dc.subjectpeptidesen
dc.subjectphaseen
dc.subjectc-13en
dc.titleSynthesis of enantiopure alpha-deuteriated Boc-L-amino acidsen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1039/P19960000537-
heal.identifier.secondary<Go to ISI>://A1996UC26300010-
heal.identifier.secondaryhttp://pubs.rsc.org/en/Content/ArticleLanding/1996/P1/p19960000537-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate1996-
heal.abstractAn alternative scheme for the synthesis of enantiopure alpha-deuteriated amino acids from a common intermediate is presented. Methyl bis(methylsulfanyl)methylene [2,2-H-2(2)] glycinate was prepared in a mixture of MeOD and D2O with a catalytic amount of Na2CO3 and attached to (2R)-bornane-10,2-sultam. Alkylation of the corresponding enolate provided intermediates which after careful purification were first deprotected on nitrogen and then cleaved from the auxiliary to give deuteriated alpha-amino acids of very high purity (> 99% ee and > 98% D). These were directly converted into the corresponding Boc-L-[2-H-2]-Ala, -Leu,-Phe and -(O-Bzl)Tyr derivatives, suitable for application in peptide synthesis, Boc-[2,2-H-2(2)]Gly was also prepared.en
heal.journalNameJournal of the Chemical Society-Perkin Transactions 1en
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ

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