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dc.creatorDjurendic, E
dc.creatorVukojevic, N
dc.creatorDramićanin, Tatjana
dc.creatorCanadi, J
dc.creatorMiljkovic, D
dc.date.accessioned2018-03-01T18:37:20Z
dc.date.available2018-03-01T18:37:20Z
dc.date.issued1998
dc.identifier.issn0352-5139
dc.identifier.urihttp://vinar.vin.bg.ac.rs/handle/123456789/2190
dc.description.abstractThe aim of this work was to synthesize 2-deoxy-2-iodo-manno sugars and 2-deoxy-2-iodo manno esters of a satisfactory purity in the highest possible yield. For this put-pose, the iodination reaction of D-glucal triacetate (1), 3,4-di-O-acetyl-6-O-to-syl-D-glucal (2) and 3,4-di-O-acetyl-6-S-acetyl-6-thio-D-glucal (3) were investigated using a mixture of NaIO4-NaI at pH 6 (acetate buffer) and pH 7 (phosphate buffer) in a tert-butanol-water solvent system. Depending on the buffer system used, a mixture of the 2-deoxy-2-iodo-manno esters 4, 6 or 8 together with corresponding 2-deoxy-2-iodo sugars 5, 7, or 9 were obtained, or separately.en
dc.rightsopenAccessen
dc.sourceJournal of the Serbian Chemical Societyen
dc.subject2-deoxy-2-iodo-manno-sugarsen
dc.subjectiodination D-glucal derivativesen
dc.subjectmodified synthesisen
dc.titleAn improved synthesis for obtaining 2-deoxy-2-iodo-D-mannopyranose derivativesen
dc.typearticleen
dcterms.abstractДјурендиц, Е; Вукојевиц, Н; Цанади, Ј; Миљковиц, Д; Драмићанин Татјана;
dc.citation.volume63
dc.citation.issue9
dc.citation.spage685
dc.citation.epage688
dc.identifier.wos000075972600002


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