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dc.creatorMihailović, Mihailo Lj.
dc.creatorLorenc, Ljubinka
dc.creatorDabović, Milan
dc.creatorJuranić, Ivan
dc.creatorWenkert, E.
dc.creatorBernassau, J.-M.
dc.creatorRaju, M S
dc.creatorMcPhail, A T
dc.creatorMiller, R W
dc.date.accessioned2019-04-26T14:01:06Z
dc.date.available2019-04-26T14:01:06Z
dc.date.issued1979
dc.identifier.issn0040-4039
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/2703
dc.description.abstractThe stereochemistries and conformations of the cyclopropane ring containing compounds derived from (E-3α- and (E)-3β-hydroxy-5,10-seco-1(10)-cholesten-5-one tosylates have been determined by X-ray methods and the results correlated with 13C nmr chemical shift data. © 1979.en
dc.publisherPergamon Press
dc.relationSerbian Academy of Sciences and Arts
dc.relationSerbian Research Fund
dc.rightsrestrictedAccess
dc.sourceTetrahedron Letters
dc.titleX-ray and carbon-13 nuclear magnetic resonance characterization of cyclopropane derivatives obtained by solvolysis of (E)-3α- and (E)-3β-hydroxy-5,10-seco-1(10)-cholesten-5-one tosylatesen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractМихаиловић, М. Љ.; Wенкерт, Е.; Бернассау, Ј.-М.; Миллер, Р W; Лоренц, Љубинка; Рају, М С; МцПхаил, A Т; Јуранић, Иван; Дабовић, М.;
dc.rights.holderElsevier B.V.
dc.citation.volume20
dc.citation.issue51
dc.citation.spage4917
dc.citation.epage4920
dc.identifier.doi10.1016/S0040-4039(01)86749-6
dc.identifier.scopus2-s2.0-49249150822
dc.type.versionpublishedVersion


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