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dc.creatorNatić, Maja
dc.creatorMarkovic, Rade
dc.creatorMilojković-Opsenica, Dušanka
dc.creatorTešić, Živoslav Lj.
dc.date.accessioned2018-11-22T00:11:31Z
dc.date.available2018-11-22T00:11:31Z
dc.date.issued2007
dc.identifier.issn1615-9306
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/879
dc.description.abstractQuantitative structure-retention relationship (QSRR) was developed for a series of the (Z)- and (E)-2-allcylidene-4-oxothiazolidine derivatives by the multiple linear regression (MLR) analysis. Full geometry optimization based on Austin Model 1 (AM1) semiempirical molecular orbital method was carried out and a set of physicochemical molecular descriptors was calculated from the optimized structures. In order to obtain useful experimental parameters, the lipophilic character of analytes was measured by RP-TLC, and lipophilicity parameters were correlated with physicochemical structural descriptors. Statistically significant and physically meaningful structure-retention relationships were obtained.en
dc.publisherWiley-V C H Verlag Gmbh, Weinheim
dc.rightsrestrictedAccess
dc.sourceJournal of Separation Science
dc.subjectdiastereomersen
dc.subjectlipophilicityen
dc.subjectmultiple linear regressionen
dc.subjectquantitative structure retention relationshipen
dc.subjectRP-TLCen
dc.titleStructure-retention relationship study of diastereomeric (Z)- and (E)-2-alkylidene-4-oxothiazolidinesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractНатић, Маја; Тешић, Живослав Љ.; Марковиц, Раде; Милојковић-Опсеница, Душанка;
dc.citation.volume30
dc.citation.issue14
dc.citation.spage2241
dc.citation.epage2248
dc.identifier.wos000249800300010
dc.identifier.doi10.1002/jssc.200700152
dc.citation.other30(14): 2241-2248
dc.citation.rankM21
dc.identifier.pmid17685377
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-34848918147
dc.identifier.rcubKon_1832


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Приказ основних података о документу