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