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dc.creatorMalinar, M.J.
dc.creatorMiodragović Đenana U.
dc.creatorMilosavljevic, S
dc.creatorCelap, MB
dc.creatorVucelic, D
dc.date.accessioned2018-11-22T00:02:25Z
dc.date.available2018-11-22T00:02:25Z
dc.date.issued1998
dc.identifier.issn1024-2430
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/402
dc.description.abstractFour out of six theoretically possible isomers of the (1,3-diaminopropane)bis(S-tyrosinato)cobalt(III) complex, having the cis(O) configuration, were isolated, and the trans(O) isomer was only defined in the eluate. The isomers were separated on an optically active Sephadex QAE column. Geometrical and absolute configurations of the isomers were determined by electronic absorption, circular dichroic and H-1 NMR spectra. The effect of the aromatic side group of the coordinated S-tyrosinato ligand on the stereoselective formation of the obtained isomers was examined.en
dc.publisherGordon Breach Sci Publ Ltd, Reading
dc.rightsrestrictedAccess
dc.sourceEnantiomer
dc.subjectCDen
dc.subjectcobalt(III) complexes,en
dc.subjectH-1 NMRen
dc.subjectstereoselectivityen
dc.subjectS-tyrosineen
dc.subjectsynthesisen
dc.titleMixed cobalt(III) complexes with S-tyrosine and 1,3-diaminopropaneen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractВуцелиц, Д; Милосављевиц, С; Малинар, МЈ; Целап, МБ; Миодраговиц, ДУ;
dc.citation.volume3
dc.citation.issue4-5
dc.citation.spage349
dc.citation.epage356
dc.identifier.wos000077531900008
dc.citation.other3(4-5): 349-356
dc.citation.rankM21
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-0032409344
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_cherry_402


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