Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/11376
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dc.contributor.authorMiljković, Dušanen_US
dc.contributor.authorVukojević, Nadaen_US
dc.contributor.authorHadžić P.en_US
dc.contributor.authorMinic D.en_US
dc.contributor.authorHughes N.en_US
dc.contributor.authorStuart Hill M.en_US
dc.contributor.authorHarangi J.en_US
dc.date.accessioned2020-03-03T14:44:09Z-
dc.date.available2020-03-03T14:44:09Z-
dc.date.issued1990-01-01-
dc.identifier.issn1472779Xen_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/11376-
dc.description.abstractThe diastereoisomeric 1,2-O-cyclohexylidene-α-D-xylofuranose 3,5-O-methylphosphonates have been synthesized as a mixture and separated by chromatography to give the pure (RP) and (SP) forms. The related thiono- and selenono-phosphonates have also been obtained. Their 13C, 1H, 31P, and 77Se NMR spectra are discussed and NOE experiments have been used to determine the chirality at phosphorus.en
dc.relation.ispartofJournal of the Chemical Society, Perkin Transactions 2en
dc.titleSynthesis and structure assignment of the diastereoisomeric 1,2-O-cyclohexylidene-α-D-xylofuranose 3,5-O-methylphosphonates and the related thiono- And selenono-phosphonatesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.scopus2-s2.0-0345974748-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0345974748-
dc.description.versionUnknownen_US
dc.relation.lastpage1095en
dc.relation.firstpage1093en
dc.relation.issue7en
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Collections:Naučne i umetničke publikacije
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