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dc.creatorMarković, R.
dc.creatorVitnik, Ž.
dc.creatorBaranac-Stojanović, Marija
dc.creatorJuranić, Ivan O.
dc.date.accessioned2018-11-22T00:04:17Z
dc.date.available2018-11-22T00:04:17Z
dc.date.issued2002
dc.identifier.issn0308-2342
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/52
dc.description.abstractCalculations using the MNDO-PM3 method were performed to elucidate the mechanism of stereoselective base-catalyzed reaction affording exclusively (Z)-2-alkylidene-4-oxothiazolidine push-pull derivatives from the corresponding α-mercapto esters and activated β-oxonitriles in ethanol as a solvent.en
dc.rightsrestrictedAccess
dc.sourceJournal of Chemical Research. Synopses
dc.subjectMNDO-PM3en
dc.subjectZ-2-alkylidene-4-oxothiazolidineen
dc.titleMechanism of stereoselective synthesis of push-pull (Z)-4-oxothiazolidine derivatives containing an exocyclic double bond. A MNDO-PM3 Studyen
dc.typearticle
dc.rights.licenseARR
dc.citation.issue10
dc.citation.spage485
dc.citation.epage489
dc.citation.other(10): 485-489
dc.citation.rankM23
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-0036816392
dc.identifier.rcubKon_1076


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