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dc.creatorMarkovic, R
dc.creatorVitnik, Z
dc.creatorBaranac-Stojanović, Marija
dc.creatorJuranić, Ivan O.
dc.date.accessioned2018-11-22T00:05:09Z
dc.date.available2018-11-22T00:05:09Z
dc.date.issued2002
dc.identifier.issn1747-5198
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/517
dc.description.abstractCalculations using the MNDO-PM3 method were performed to elucidate the mechanism of stereoselective base-catalyzed reaction affording exclusively (2)-2-alkylidene-4-oxothiazolidine push-pull derivatives from the corresponding a-mercapto esters and activated beta-oxonitriles in ethanol as a solvent.en
dc.publisherScience Reviews 2000 Ltd, St Albans
dc.rightsrestrictedAccess
dc.sourceJournal of Chemical Research
dc.subjectMNDO-PM3en
dc.subjectZ-2-alkylidene-4-oxothiazolidineen
dc.titleMechanism of stereoselective synthesis of push-pull (2)-4-oxothiazolidine derivatives containing an exocyclic double bond. A MNDO-PM3 Studyen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractБаранац-Стојановић, Марија; Јураниц, И; Марковиц, Р; Витник, З;
dc.citation.issue10
dc.citation.spage485
dc.citation.epage489
dc.identifier.wos000179687200008
dc.citation.other(10): 485-489
dc.identifier.rcubKon_1491


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