Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/10353
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dc.contributor.authorIllyés T.en
dc.contributor.authorMolnár-Gábor D.en
dc.contributor.authorSzilágyi L.en
dc.date.accessioned2020-03-03T14:39:01Z-
dc.date.available2020-03-03T14:39:01Z-
dc.date.issued2004-06-01en
dc.identifier.issn00086215en
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/10353-
dc.description.abstractBis(tetra-O-acetyl-β-D-glucopyranosyl)disulfide reacts, under silver ion activation, with primary and secondary aliphatic as well as aromatic amines to furnish the title compounds in moderate to good yields. The same derivatives could also be obtained from (tetra-O-acetyl)-β-D-glucopyranosyl methanethiolsulfonate 1 by nucleophilic substitution with amines. It was shown that the polarization of the S-S-bond in 1 is enhanced by Ag+ so as to allow reaction with sterically hindered amines as well. © 2004 Elsevier Ltd. All rights reserved.en
dc.relation.ispartofCarbohydrate Researchen
dc.titleNovel approaches to the syntheses of N-substituted S-glycosyl-sulfenamidesen
dc.typeJournal/Magazine Articleen
dc.identifier.doi10.1016/j.carres.2004.03.023en
dc.identifier.pmid339en
dc.identifier.scopus2-s2.0-2642556156en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/2642556156en
dc.relation.lastpage1564en
dc.relation.firstpage1561en
dc.relation.issue8en
dc.relation.volume339en
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Collections:Naučne i umetničke publikacije
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