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dc.creatorMilosavljević, Milutin M.
dc.creatorSovrlić, Milica
dc.creatorMarinković, Aleksandar
dc.creatorMilenković, Dragan D.
dc.date.accessioned2021-03-10T11:20:28Z
dc.date.available2021-03-10T11:20:28Z
dc.date.issued2010
dc.identifier.issn0026-9247
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/1660
dc.description.abstractA novel synthesis of N-alkyl and N,N-dialkyl O-ethyl thiocarbamates from diethyl dixanthogenate and primary and secondary amines, using three oxidizing systems, has been developed on the laboratory scale, and the method using sodium hypochlorite has been applied on a semi-industrial scale. The effect of the oxidizing agents, sodium hypochlorite, in-situ-generated peracetic acid, and the manganese(II) acetate/oxygen system on product purity and yield was studied. The results obtained by use of these three methods were compared with those obtained by reaction of sodium ethyl xanthogenacetate and amines, and of sodium ethyl xanthate with amines in the presence of sulfated nickel zeolite catalyst. The reaction mechanism of sodium hypochlorite oxidation has been established on the basis of isolation of reaction intermediates and determination of their structure by use of Fourier-transform infrared, (1)H and (13)C NMR, and mass spectrometric methods. The suggested sodium hypochlorite and manganese(II) acetate/oxygen systems have many advantages in comparison with commercial and catalytically promoted synthetic methods, because they are new ecologically friendly syntheses.en
dc.publisherSpringer Wien, Wien
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142063/RS//
dc.rightsrestrictedAccess
dc.sourceMonatshefte Fur Chemie
dc.subjectDiethyl dixanthogenateen
dc.subjectThiocarbamatesen
dc.subjectSodium hypochloriteen
dc.subjectManganese(II) acetateen
dc.subjectPeracetic aciden
dc.subjectSulfated nickel zeolite catalysten
dc.titleA synthesis of N-alkyl and N,N-dialkyl O-ethyl thiocarbamates from diethyl dixanthogenate using different oxidantsen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage755
dc.citation.issue7
dc.citation.other141(7): 749-755
dc.citation.rankM22
dc.citation.spage749
dc.citation.volume141
dc.identifier.doi10.1007/s00706-010-0328-y
dc.identifier.scopus2-s2.0-78149413895
dc.identifier.wos000279698600005
dc.type.versionpublishedVersion


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