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dc.creatorBaranac-Stojanović, Marija
dc.creatorTatar, Jovana
dc.creatorKleinpeter, Erich
dc.creatorMarković, Rade
dc.date.accessioned2019-01-30T17:18:39Z
dc.date.available2019-01-30T17:18:39Z
dc.date.issued2008
dc.identifier.issn0039-7881
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/457
dc.description.abstractA new series of unsubstituted and substituted pyridinium salts bearing a 4-oxothiazolidinyl moiety has been prepared by an efficient rearrangement of 2-(l-bromoalkylidene)thiazolidin-4-ones. The process is based on three steps, namely carbon - bromine cleavage, bromine transfer, and substitution, each induced by pyridine or its derivatives, acting as base and reactant.en
dc.publisherGeorg Thieme Verlag Kg, Stuttgart
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142007/RS//
dc.rightsrestrictedAccess
dc.sourceSynthesis
dc.subject4-oxothiazolidineen
dc.subjectBromine transferen
dc.subjectCarbon-bromine cleavageen
dc.subjectNucleophilic substitutionen
dc.subjectPyridinium saltsen
dc.subjectRearrangementen
dc.titleHigh-yield synthesis of substituted and unsubstituted pyridinium salts containing a 4-oxothiazolidine moietyen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractТатар, Јована; Баранац-Стојановић, М.; Клеинпетер, Е.; Марковић, Р.;
dc.citation.issue13
dc.citation.spage2117
dc.citation.epage2121
dc.citation.other(13): 2117-2121
dc.citation.rankM22
dc.identifier.doi10.1055/s-2008-1067113
dc.identifier.rcubConv_4162
dc.identifier.scopus2-s2.0-47349129385
dc.identifier.wos000257710900021
dc.type.versionpublishedVersion


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