Please use this identifier to cite or link to this item:
https://open.uns.ac.rs/handle/123456789/13861
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lazar D. | en_US |
dc.contributor.author | Stanković S. | en_US |
dc.contributor.author | Pejanović V. | en_US |
dc.contributor.author | Courseille C. | en_US |
dc.date.accessioned | 2020-03-03T14:53:59Z | - |
dc.date.available | 2020-03-03T14:53:59Z | - |
dc.date.issued | 2002-01-01 | - |
dc.identifier.issn | 01082701 | en_US |
dc.identifier.uri | https://open.uns.ac.rs/handle/123456789/13861 | - |
dc.description.abstract | The conformations of two secoestrone derivatives, C25H27NO2 and C25H29NO2 were determined. The compounds exhibited different conformations in the solid state, which was responsible for the difference in the biological activity of the compounds. The compounds were synthesized from natural oestrone and their x ray structures were described. | en |
dc.relation.ispartof | Acta Crystallographica Section C: Crystal Structure Communications | en |
dc.title | D-Secoestrone derivatives. V. 3-Methoxy-17-oxo-17-phenyl-16,17-secoestra-1,3,5(10)-triene-16-nitrile and 17-hydroxy-3-methoxy-17-phenyl-16,17-secoestra-1,3,5(10)-triene-16-nitrile | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.doi | 10.1107/S0108270101018182 | - |
dc.identifier.scopus | 2-s2.0-0036486980 | - |
dc.identifier.url | https://api.elsevier.com/content/abstract/scopus_id/0036486980 | - |
dc.description.version | Unknown | en_US |
dc.relation.lastpage | o65 | en |
dc.relation.firstpage | o63 | en |
dc.relation.issue | 2 | en |
dc.relation.volume | 58 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | Naučne i umetničke publikacije |
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