Приказ основних података о документу

dc.creatorLorenc, Ljubinka
dc.creatorDabović, Milan
dc.creatorJuranić, Ivan
dc.creatorMihailović, Milhailo Lj.
dc.creatorSnatzke, G
dc.creatorTóth, G
dc.date.accessioned2019-04-26T10:20:11Z
dc.date.available2019-04-26T10:20:11Z
dc.date.issued1982
dc.identifier.issn0040-4020
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/2696
dc.description.abstractCircular dichroism of the rearranged keto steroids 3 and 4, containing a condensed three and nine-membered ring system, shows that the conformation of the nine-membered ring is the same in solution as in the crystal; reduction of the kto group does not change this situation. CD also indicates that epimerization at C(5) in the pair 7 8 and the pair 11 12 leaves the cyclononanone ring conformation unchanged. © 1982.en
dc.publisherElsevier
dc.relationSerbian Research Fund
dc.relationSerbian Academy of Sciences and Arts
dc.relationDeutsche Furschungsgemeinschaft
dc.relationFunds der Chemischen Industrie
dc.relationAlexander von Humboldt Foundation (Germany)
dc.rightsrestrictedAccess
dc.sourceTetrahedron
dc.titleCircular dichroism of some cyclopropane ring containing 1,3-cyclo-5,10-seco-steroidal ketonesen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractМихаиловић, М. Љ.; Дабовић, М.; Јуранић, Иван; Тóтх, Г; Лоренц, Љубинка; Снатзке, Г;
dc.rights.holderElsevier
dc.citation.volume38
dc.citation.issue21
dc.citation.spage3163
dc.citation.epage3168
dc.identifier.doi10.1016/0040-4020(82)80053-7
dc.identifier.scopus2-s2.0-49049137738
dc.type.versionpublishedVersion


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Приказ основних података о документу