O-17 NMR studies of electronic and steric interactions of substituted quinoxaline-2(1H),3(4H)-diones

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dc.contributor.authorGerothanassis, I. P.en
dc.contributor.authorVarvounis, G.en
dc.date.accessioned2015-11-24T16:43:02Z
dc.date.available2015-11-24T16:43:02Z
dc.identifier.issn0022-152X-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8636
dc.rightsDefault Licence-
dc.subjectreceptor antagonistsen
dc.subjectspectroscopyen
dc.subjectpeptidesen
dc.subjectamidesen
dc.subjectDNAen
dc.titleO-17 NMR studies of electronic and steric interactions of substituted quinoxaline-2(1H),3(4H)-dionesen
heal.abstractO-17 nmr studies, at natural abundance, of substituted quinoxarine-2(1H),3(4H)-diones demonstrate that the O-17 chemical shift data can provide new insights into steric and electronic interactions due to long range substituent effects on the aromatic ring. The role of considerable ''keto'' character and torsion angle deformation of the diamide group in solution is emphasized.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondary<Go to ISI>://A1996VC21600021-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/jhet.5570330320/asset/5570330320_ftp.pdf?v=1&t=hmrgg3yc&s=68cded4411bdc134d513e8982bf53ee4d762a39a-
heal.journalNameJournal of Heterocyclic Chemistryen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate1996-
heal.publisherWiley-Blackwellen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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