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Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones
dc.creator | Popov-Pergal, Katarina M. | |
dc.creator | Poleti, Dejan | |
dc.creator | Rancic, Milica P. | |
dc.creator | Meden, Antun | |
dc.creator | Pergal, Marija | |
dc.date.accessioned | 2019-01-30T17:24:39Z | |
dc.date.accessioned | 2023-01-23T12:06:42Z | |
dc.date.available | 2019-01-30T17:24:39Z | |
dc.date.available | 2023-01-23T12:06:42Z | |
dc.date.issued | 2010 | |
dc.identifier.issn | 0022-152X | |
dc.identifier.uri | http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5616 | |
dc.description.abstract | The derivatives of 5-substituted-2,4-thiazolidinedione have a broad spectrum of biological activities. In this article, new 5-(arylidene)-3-(4-methylbenzoyl)thiayolidine-2,4-diones 3a-k, with arylidene groups such as 4-phenylbenzylidene 3a, 3,4-dimethoxybenzylidene 3b, 2-hydroxybenzylidene 3c, 4-ethoxybenzylidene 3d, 5-methyl-2-furfurylidene 3e, 4-dimethylaminobenzylidene 3f, 1-naphthylidene 3g, 3,4-methylenedioxybenzylidene 3h, 4-benzyloxybenzylidene 3i, benzylidene 3j, and 4-methoxybenzylidene 3k, were synthesized by direct acylation of alkali metal salts of 5-arylidene-2,4-thiazolidinediones with 4-methylbenzoylchloride. Their structures were confirmed by elemental analysis, IR, (1)H NMR and MS spectroscopy. In addition, crystal structure of the compound 3d was determined using single-crystal X-ray diffraction data. | en |
dc.publisher | Wiley-Blackwell Publishing, Inc, Malden | |
dc.relation | Ministry of Science and Technological Development of the Republic of Serbia - 1694 | |
dc.relation | info:eu-repo/grantAgreement/MESTD/MPN2006-2010/142030/RS// | |
dc.relation | info:eu-repo/grantAgreement/MESTD/MPN2006-2010/142023/RS// | |
dc.rights | restrictedAccess | |
dc.source | Journal of Heterocyclic Chemistry | |
dc.title | Synthesis and Structure of New 5-(Arylidene)-3-(4-methylbenzoyl)thiazolidine-2,4-diones | en |
dc.type | article | |
dc.rights.license | ARR | |
dc.citation.epage | 228 | |
dc.citation.issue | 1 | |
dc.citation.other | 47(1): 224-228 | |
dc.citation.rank | M23 | |
dc.citation.spage | 224 | |
dc.citation.volume | 47 | |
dc.identifier.doi | 10.1002/jhet.288 | |
dc.identifier.scopus | 2-s2.0-76149087496 | |
dc.identifier.wos | 000274490300037 | |
dc.type.version | publishedVersion |