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dc.creatorGođevac, Dejan
dc.creatorMandić, Boris
dc.creatorVajs, Vlatka
dc.creatorMenkovic, N.
dc.creatorMacura, S.
dc.creatorMilosavljević, Slobodan M.
dc.date.accessioned2018-11-22T00:09:47Z
dc.date.available2018-11-22T00:09:47Z
dc.date.issued2006
dc.identifier.issn0749-1581
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/784
dc.description.abstractLeucanthoside A, a new allose-containing triterpenoid saponin (1), was isolated from the aerial parts of Cephalaria leucantha L. Its structure was determined by electrospray ionization mass spectrometry and NMR spectroscopy. Complete assignments of the H-1 and 1 C NMR chemical shifts were achieved by two-dimensional NMR experiments: DQF-COSY, NOESY, TOCSY, HSQC, DINE-HSQC, HMBC, C-13-H-1 2D-J-resolved spectroscopy, and 1,1-ADEQUATE. Copyright (c) 2006 John Wiley & Sons, Ltd.en
dc.publisherJohn Wiley & Sons Ltd, Chichester
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142053/RS//
dc.rightsrestrictedAccess
dc.sourceMagnetic Resonance in Chemistry
dc.subjectNMRen
dc.subjectH-1 NMRen
dc.subjectC-13 NMRen
dc.subject2D NMRen
dc.subjectCephalaria leucanthaen
dc.subjectsaponinen
dc.subjectleucanthoside Aen
dc.titleComplete assignments of H-1 and C-13 NMR spectra of leucanthoside A, a new triterpenoid saponin from Cephalaria leucantha L.en
dc.typearticle
dc.rights.licenseARR
dcterms.abstractМилосављевиц, С.; Мацура, С.; Вајс, В.; Менковиц, Н.; Мандић, Борис; Годевац, Д.;
dc.citation.volume44
dc.citation.issue7
dc.citation.spage731
dc.citation.epage735
dc.identifier.wos000238691300014
dc.identifier.doi10.1002/mrc.1834
dc.citation.other44(7): 731-735
dc.citation.rankM22
dc.identifier.pmid16645935
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-33745712031
dc.identifier.rcubKon_1737


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