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dc.contributor.authorBalayiannis, G.en
dc.contributor.authorPapaioannou, D.en
dc.contributor.authorTroganis, A.en
dc.date.accessioned2015-11-24T16:32:41Z-
dc.date.available2015-11-24T16:32:41Z-
dc.identifier.issn0749-1581-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/7576-
dc.rightsDefault Licence-
dc.subjectnmren
dc.subjecthnmren
dc.subjectc-13 nmren
dc.subjectnucleoside analoguesen
dc.subjectconformationen
dc.subjectconfigurationen
dc.titleConfiguration and conformation of a novel uridine analogue: H-1 and C-13 NMR spectra of (5 ' S)-1-[2 '-(2-hydroxyethyl)tetrahydropyran-5 '-yl]-1H-pyrimidine-2,4-dioneen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDoi 10.1002/Mrc.1001-
heal.identifier.secondary<Go to ISI>://000174026600014-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/mrc.1001/asset/1001_ftp.pdf?v=1&t=h1q2bwq4&s=6b0c69f06a7fba609042d9bbb446e76dcf230ee6-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιώνel
heal.publicationDate2002-
heal.abstractA combination of homo- and heteronuclear 1D and 2D NMR techniques provided the assignment of the H-1 and C-13 resonances of the major component of a reaction product consisting of the two possible diastereomers of (5'S)-1-[2'-(2-hydroxyethyl)tetrahydropyran-5'-yl]-1H-pyrimidine-2,4-dione and showed that the tetrahydropyranyl ring in the major 5S,2'S-isomer adopts the twist conformation. Copyright (C) 2002 John Wiley Sons, Ltd.en
heal.journalNameMagnetic Resonance in Chemistryen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

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