Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/13861
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dc.contributor.authorLazar D.en_US
dc.contributor.authorStanković S.en_US
dc.contributor.authorPejanović V.en_US
dc.contributor.authorCourseille C.en_US
dc.date.accessioned2020-03-03T14:53:59Z-
dc.date.available2020-03-03T14:53:59Z-
dc.date.issued2002-01-01-
dc.identifier.issn01082701en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/13861-
dc.description.abstractThe 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.ispartofActa Crystallographica Section C: Crystal Structure Communicationsen
dc.titleD-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-nitrileen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1107/S0108270101018182-
dc.identifier.scopus2-s2.0-0036486980-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0036486980-
dc.description.versionUnknownen_US
dc.relation.lastpageo65en
dc.relation.firstpageo63en
dc.relation.issue2en
dc.relation.volume58en
item.fulltextNo Fulltext-
item.grantfulltextnone-
Appears in Collections:Naučne i umetničke publikacije
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