Приказ основних података о документу

dc.creatorLorenc, Ljubinka
dc.creatorJuranić, Ivan
dc.creatorDabović, Milan
dc.creatorMihailović, Milhailo Lj.
dc.date.accessioned2019-04-26T11:16:42Z
dc.date.available2019-04-26T11:16:42Z
dc.date.issued1991
dc.identifier.issn0040-4020
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/2698
dc.description.abstractUV irradiation of the steroidal isoxazolidines 2a, 2b, and 2c in various solvents in the presence of molecular oxygen, results in oxidative cleavage of the epoxyimino bridge to give several products; the N-unsubstituted isoxazolidine 2a afforded the nitro products 3, 4, and 5 and the azoxy compounds 6 and 7, while the N-methyl and N-acetyl derivatives 2b and 2c produced only the nitro compounds 3 and 5 as sole identifiable material. An explanation of the observed photooxygenation processes involving exciplex formation followed by proton transfer from isaxazolidine to molecular oxygen is presented. © 1991.en
dc.publisherPergamon press
dc.relationSerbian Academy of Sciences and Arts
dc.relationSerbian Republic Research Fund
dc.rightsrestrictedAccess
dc.sourceTetrahedron
dc.subjectIsoxamlidines
dc.subjectTriplet Oxygen
dc.subjectPhotooxygenation
dc.subjectExciplex
dc.subjectSteroids
dc.titleNon-sensitized photooxygenation of some steroidal isoxazolidinesen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractДабовић, Милан; Михаиловић, М. Љ.; Лоренц, Љубинка; Јуранић, Иван;
dc.rights.holderElsevier
dc.citation.volume47
dc.citation.issue32
dc.citation.spage6389
dc.citation.epage6398
dc.identifier.doi10.1016/S0040-4020(01)86567-4
dc.identifier.scopus2-s2.0-0025850238
dc.type.versionpublishedVersion


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Приказ основних података о документу