Приказ основних података о документу

dc.creatorRajković, Milica M.
dc.creatorLorenc, Ljubinka
dc.creatorPetrović, Ivanka
dc.creatorMilovanović, Aleksandar Ž.
dc.creatorMihailović, Milhailo Lj.
dc.date.accessioned2021-03-16T11:38:42Z
dc.date.available2021-03-16T11:38:42Z
dc.date.issued1991
dc.identifier.issn0040-4039
dc.identifier.issn1873-3581
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4362
dc.description.abstractTreatment of steroidal isoxazolidines 3a, 3b and 5b with N-methylhydroxylamine hydrochloride in boiling ethanol-pyridine (1:1) solution results in elimination of the CH3NH2fragment, affording products of oxidative hydrolysis 4a, 4b, and 6b, while acid-catalyzed reaction of isoxazolidines 2a, 3a and 5b leads to rearrangement involving the N-CH3 group with formation of the perhydro-3,1-oxazine derivatives 8a, 9a and 10b.sr
dc.language.isoensr
dc.publisherElseviersr
dc.rightsrestrictedAccesssr
dc.sourceTetrahedron Letterssr
dc.subject1-oxazinessr
dc.subjectacid-catalyzed rearrangementsr
dc.subjectoxidative hydrolysissr
dc.subjectstereoidal perhydro-3sr
dc.subjectsteroidal isoxazolidinessr
dc.titleOxidative hydrolysis and acid-catalyzed rearrangement of steroidal isoxazolidinessr
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractПетровић, Иванка; Рајковић, Милица М.; Лоренћ, Љубинка Б.; Михаиловíћ, Милхаило Љ.; Миловановић, Aлександар Ж.;
dc.citation.volume32
dc.citation.issue51
dc.citation.spage7605
dc.citation.epage7608
dc.identifier.doi10.1016/0040-4039(91)80546-I
dc.identifier.scopus2-s2.0-0026335197
dc.type.versionpublishedVersionsr


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Приказ основних података о документу