O-17 and N-14 NMR studies of quinoxaline-2(1H),3(4H)-diones and N,N'-substituted oxamides: The first experimental evidence of torsion angle deformation resulting from an unprecedented through six-bond substituent effect on the diamide group of quinoxaline-2(1H),3(4H)-diones

dc.contributor.authorGerothanassis, I. P.en
dc.contributor.authorCobb, J.en
dc.contributor.authorKimbaris, A.en
dc.contributor.authorSmith, J. A. S.en
dc.contributor.authorVarvounis, G.en
dc.date.accessioned2015-11-24T16:43:00Z
dc.date.available2015-11-24T16:43:00Z
dc.identifier.issn0040-4039-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8633
dc.rightsDefault Licence-
dc.subjectreceptor antagonistsen
dc.subjectspectroscopyen
dc.subjectDNAen
dc.titleO-17 and N-14 NMR studies of quinoxaline-2(1H),3(4H)-diones and N,N'-substituted oxamides: The first experimental evidence of torsion angle deformation resulting from an unprecedented through six-bond substituent effect on the diamide group of quinoxaline-2(1H),3(4H)-dionesen
heal.abstractO-17 and N-14 NMR studies of quinoxaline-2(1H),3(4H)-diones demonstrate a significant torsion angle deformation of the diamide group in solution due to an unprecedented through six bond substituent effect. Copyright (C) 1996 Elsevier Science Ltden
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1016/0040-4039(96)00492-3-
heal.identifier.secondary<Go to ISI>://A1996UH38100031-
heal.identifier.secondaryhttp://ac.els-cdn.com/0040403996004923/1-s2.0-0040403996004923-main.pdf?_tid=ae577dac-34ac-11e3-8c43-00000aacb362&acdnat=1381740381_deb11ad70cbc13593e7100ae1117015c-
heal.journalNameTetrahedron Letten
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate1996-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

Αρχεία

Φάκελος/Πακέτο αδειών

Προβολή: 1 - 1 of 1
Φόρτωση...
Μικρογραφία εικόνας
Ονομα:
license.txt
Μέγεθος:
1.74 KB
Μορφότυπο:
Item-specific license agreed upon to submission
Περιγραφή: