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dc.creatorKalvoda, Jaroslav
dc.creatorGrob, Jüren
dc.creatorBjelaković, Mira
dc.creatorLorenc, Ljubinka
dc.creatorMihailović, Milhailo Lj.
dc.date.accessioned2021-02-02T09:39:18Z
dc.date.available2021-02-02T09:39:18Z
dc.date.issued1997
dc.identifier.issn0018-019X
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4188
dc.description.abstractThe two structurally similar 20‐phenyl‐ and 20‐(4‐methoxyphenyl)‐11‐(nitrosooxy)pregnan‐20‐ol derivatives 4 and 7 behave differently under photolytic conditions, the former nitrous acid ester affording, as a main product, the benzo‐fused hexacyclic compound 9, and the latter the 21‐nitro derivative 12. Mechanistic aspects of these transformations are discussed.
dc.publisherWileyen
dc.relationSerbian Academy of Sciences and Arts
dc.relationMinistry of Sciences and Technology of Serbia
dc.rightsrestrictedAccess
dc.sourceHelvetica Chimica Actaen
dc.subjectSteroids
dc.subjectPhotolysis
dc.subjectrearrangement
dc.titlePhotolysis of Steroidal 20-Aryl-Substituted 11-Nitritesen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractКалвода, Јарослав; Михаиловић, Михаило Љ.; Бјелаковић, Мира; Лоренц, Љубинка; Гроб, Јüрен;
dc.citation.volume80
dc.citation.issue4
dc.citation.spage1221
dc.citation.epage1228
dc.identifier.doi10.1002/hlca.19970800419
dc.identifier.scopus2-s2.0-0009548873
dc.type.versionpublishedVersion


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