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dc.creatorNatić, Maja
dc.creatorMarkovic, R
dc.creatorAnđelković, Katarina K.
dc.creatorMilojković-Opsenica, Dušanka
dc.creatorTešić, Živoslav Lj.
dc.date.accessioned2018-11-22T00:07:34Z
dc.date.available2018-11-22T00:07:34Z
dc.date.issued2004
dc.identifier.issn0933-4173
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/673
dc.description.abstractExperimental R, values for a series of functionalized 2-alkylidene-4-oxothiazolidines and 1,2-dithioles have been determined by reversed-phase TLC on RP-18 silica plates. Binary mixtures of methanol and water, tetrahydrofuran and water, and acetone and water were used as mobile phases. R-M(0) values were determined for these mobile phase mixtures by linear extrapolation to 0% (v/v) organic modifier. The lipophilicity, C-0, was calculated as the ratio of the intercept and slope values. Chromatographically obtained lipophilicity data correlated well with calculated log P values.en
dc.publisherResearch Inst Medicinal Plants, Budakalasz
dc.rightsrestrictedAccess
dc.sourceJournal of Planar Chromatography: Modern TLC / Thin Layer Chromatography
dc.subject2-alkylidene-4-oxothiazolidinesen
dc.subject1,2-dithiolesen
dc.subjectreversed-phase TLCen
dc.subjectlipophilicityen
dc.titleReversed-phase thin-layer chromatography of stereodefined 2-alkylidene-4-oxothiazolidines and 1,2-dithiolesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractAнђелковић, Катарина; Марковиц, Р; Натић, Маја; Тешић, Живослав Љ.; Милојковић-Опсеница, Душанка;
dc.citation.volume17
dc.citation.issue5
dc.citation.spage323
dc.citation.epage327
dc.identifier.wos000225586900001
dc.identifier.doi10.1556/JPC.17.2004.5.1
dc.citation.other17(5): 323-327
dc.citation.rankM23
dc.identifier.scopus2-s2.0-9744220434
dc.identifier.rcubKon_1625


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