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dc.creatorVajs, Vlatka
dc.creatorJeremić, Dragoslav
dc.creatorMilosavljević, Slobodan
dc.creatorMacura, Slobodan
dc.date.accessioned2019-04-30T13:11:15Z
dc.date.available2019-04-30T13:11:15Z
dc.date.issued1987
dc.identifier.issn0749-1581
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/2784
dc.description.abstractThe application of two‐dimensional NOE NMR spectroscopy (NOESY) for the stereochemical assignment of isomeric 14‐acetoxy‐13‐hydroxy‐ and 13‐acetoxy‐14‐hydroxy‐5,6‐caryophyllen‐7‐ones, and their acetylation products, is reported. Copyright © 1987 John Wiley & Sons Ltd.en
dc.publisherJohn Wiley & Sons Ltd.
dc.relationSerbian Republic Research Fund
dc.rightsrestrictedAccess
dc.sourceMagnetic Resonance in Chemistry
dc.subjectNOESY
dc.subject2D NMR
dc.subject14-acetoxy-l3-hydroxy-5,6-caryophyllen-7-ones
dc.subject13-acetoxy-14-hydroxy-5,6-caryophyllen-7-ones
dc.subjectsesquiterpenes
dc.titleTwo‐dimensional NMR spectra of sesquiterpenes. I—NOESY study of caryophyllenes from Inula spiraeifoliaen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractМилосављевић, Слободан; Вајс, Влатка; Мацура, Слободан; Јеремић, Драгослав;
dc.rights.holderJohn Wiley & Sons Ltd.
dc.citation.volume25
dc.citation.issue10
dc.citation.spage889
dc.citation.epage891
dc.identifier.doi10.1002/mrc.1260251012
dc.identifier.scopus2-s2.0-84989640924
dc.type.versionpublishedVersion


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Приказ основних података о документу