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dc.creatorMihailović, Mihailo
dc.creatorLorenc, Ljubinka
dc.creatorGašić, Miroslav J.
dc.creatorRogić, Milorad
dc.creatorMelera, A.
dc.creatorStefanović, Milutin
dc.date.accessioned2021-01-27T22:08:39Z
dc.date.available2021-01-27T22:08:39Z
dc.date.issued1966
dc.identifier.issn0040-4020
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4161
dc.description.abstractAssignment of configuration to the 1,10-double bond in the cis-trans isomeric 3β-acetoxy-5,10-seco-1,10-cholesten-5-ones has been achieved by means of NMR spectrometry. Some reactions of these new compounds have been studied and, as expected from conformational analysis, it was found that only the trans-isomer readily undergoes transannular cyclizationssr
dc.language.isoensr
dc.publisherElseviersr
dc.rightsrestrictedAccesssr
dc.sourceTetrahedronsr
dc.subjectcis-transsr
dc.subjectisomerisationsr
dc.subjectsteroidssr
dc.subjectconfigurationsr
dc.subjectNMR spectrometrysr
dc.subjectConformational Analysissr
dc.subjecttransannular cyclizationssr
dc.titleConfiguration and reactivity of ten-membered 5,10-seco-compounds obtained by fragmentation of 5-hydroxy-steroidssr
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractГашић, Мирослав; Лоренц, Љубинка; Стефановић, Милутин; Мелера, A.; Рогић, Милорад; Михаиловић, Михаило;
dc.citation.volume22
dc.citation.issue7
dc.citation.spage2345
dc.citation.epage2358
dc.identifier.doi10.1016/S0040-4020(01)82154-2
dc.identifier.scopus2-s2.0-0011723530
dc.type.versionpublishedVersionsr


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