dc.creator | Kalvoda, Jaroslav | |
dc.creator | Grob, Jüren | |
dc.creator | Bjelaković, Mira | |
dc.creator | Lorenc, Ljubinka | |
dc.creator | Mihailović, Milhailo Lj. | |
dc.date.accessioned | 2021-02-02T09:39:18Z | |
dc.date.available | 2021-02-02T09:39:18Z | |
dc.date.issued | 1997 | |
dc.identifier.issn | 0018-019X | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/4188 | |
dc.description.abstract | The 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.publisher | Wiley | en |
dc.relation | Serbian Academy of Sciences and Arts | |
dc.relation | Ministry of Sciences and Technology of Serbia | |
dc.rights | restrictedAccess | |
dc.source | Helvetica Chimica Acta | en |
dc.subject | Steroids | |
dc.subject | Photolysis | |
dc.subject | rearrangement | |
dc.title | Photolysis of Steroidal 20-Aryl-Substituted 11-Nitrites | en |
dc.type | article | en |
dc.rights.license | ARR | |
dcterms.abstract | Калвода, Јарослав; Михаиловић, Михаило Љ.; Бјелаковић, Мира; Лоренц, Љубинка; Гроб, Јüрен; | |
dc.citation.volume | 80 | |
dc.citation.issue | 4 | |
dc.citation.spage | 1221 | |
dc.citation.epage | 1228 | |
dc.identifier.doi | 10.1002/hlca.19970800419 | |
dc.identifier.scopus | 2-s2.0-0009548873 | |
dc.type.version | publishedVersion | |