Please use this identifier to cite or link to this item:
https://open.uns.ac.rs/handle/123456789/9894
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Miljković D. | en |
dc.contributor.author | Petrović J. | en |
dc.contributor.author | Hadžić P. | en |
dc.date.accessioned | 2020-03-03T14:35:45Z | - |
dc.date.available | 2020-03-03T14:35:45Z | - |
dc.date.issued | 1978-01-01 | en |
dc.identifier.issn | 00404020 | en |
dc.identifier.uri | https://open.uns.ac.rs/handle/123456789/9894 | - |
dc.description.abstract | The Beckmann fragmentation product, 3-methoxy-17-oxo-16,17-secoestra-1,3,5(10)-trien-16-nitrile (2) has been reduced by LAH giving the expected 3-methoxy-17-hydroxy-16,17-secoestra-1,3,5(10-trien-16-amine hydrochloride (3) and 3-methoxy-17-oxa-D-homoestra-1,3,5(10)-trien-16-ol (4), by a presumed neighbouring group participation of 17-OH group in the intermediary formed 16-imino derivative (A). The structure of 4 has been proved by an alternative synthetic route by reducing 3-methoxy-17-oxa-D-homoestra-1,3,5(10)-trien-16-one (7) with di-iso-butylaluminium hydride. © 1978. | en |
dc.relation.ispartof | Tetrahedron | en |
dc.title | Some new ring-D seco steroids | en |
dc.type | Journal/Magazine Article | en |
dc.identifier.doi | 10.1016/0040-4020(78)88434-8 | en |
dc.identifier.scopus | 2-s2.0-0018216932 | en |
dc.identifier.url | https://api.elsevier.com/content/abstract/scopus_id/0018216932 | en |
dc.relation.lastpage | 3577 | en |
dc.relation.firstpage | 3575 | en |
dc.relation.issue | 24 | en |
dc.relation.volume | 34 | en |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
Appears in Collections: | Naučne i umetničke publikacije |
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