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A novel procedure for the aromatization of ring a in 19-nortestosterone
dc.creator | Mihalilović, M.Lj. | |
dc.creator | Foršek, Jože | |
dc.creator | Lorenc, Ljubinka B. | |
dc.date.accessioned | 2021-05-10T15:20:29Z | |
dc.date.available | 2021-05-10T15:20:29Z | |
dc.date.issued | 1977 | |
dc.identifier.issn | 0040-4020 | |
dc.identifier.issn | 1464-5416 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/4581 | |
dc.description.abstract | A convenient, 40% overall yield synthesis of 2,3,17β-triacetoxy-1,3,5(10)-estratriene is described, which involves epoxidation of 19-nortestosterone and subsequent acetylation, lead tetra-acetate acetoxylation of the so-formed 17β-acetoxy-4β,5-epoxy-5β-estran-3-one, and aromatization of ring A, by means of acidic alumina, of the resulting 2α and 2β epimers of 2,17β-diacetoxy-4β,5-epoxy-5β-estran-3-one. | sr |
dc.language.iso | en | sr |
dc.publisher | Elsevier | sr |
dc.relation | The Research Fund of the Republic of Serbia | sr |
dc.relation | The Serbian Academy of Sciences and Arts | sr |
dc.rights | restrictedAccess | sr |
dc.source | Tetrahedron | sr |
dc.subject | aromatization of ring | sr |
dc.subject | acetylation | sr |
dc.subject | acidic alumina | sr |
dc.title | A novel procedure for the aromatization of ring a in 19-nortestosterone | sr |
dc.type | article | sr |
dc.rights.license | ARR | sr |
dcterms.abstract | Михалиловић, М.Љ.; Лоренц, Љубинка Б.; Форшек, Јоже; | |
dc.citation.volume | 33 | |
dc.citation.issue | 2 | |
dc.citation.spage | 235 | |
dc.citation.epage | 237 | |
dc.identifier.doi | 10.1016/0040-4020(77)80132-4 | |
dc.identifier.scopus | 2-s2.0-0344203618 | |
dc.type.version | publishedVersion | sr |