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dc.contributor.authorHaarr, Marianne Bore
dc.contributor.authorLindback, Emil
dc.contributor.authorHåland, Torfinn
dc.contributor.authorSydnes, Magne Olav
dc.date.accessioned2023-07-18T08:44:41Z
dc.date.available2023-07-18T08:44:41Z
dc.date.created2018-07-06T00:57:48Z
dc.date.issued2018-07
dc.identifier.citationHaarr, M.B., Lindbäck, E., Håland, T., & Sydnes, M.O. (2018) Synthesis of an Alleged Byproduct Precursor in Iodixanol Preparation. ACS Omega, 3 (7), 7344-7349.en_US
dc.identifier.issn2470-1343
dc.identifier.urihttps://hdl.handle.net/11250/3079680
dc.description.abstractN1,N3-Bis(2,3-dihydroxypropyl)-2,4,6-triiodo-5-(N-(oxiran-2-ylmethyl)acetamido)isophthalamide (1), the alleged precursor of several minor byproducts formed when the X-ray contrast agent iodixanol is synthesized from 5-acetamido-N1,N3-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide (2), has been successfully prepared with an overall yield of 25%. Epoxide 1 enabled the confirmation of its presence in the reaction mixture during the preparation of iodixanol when amide 2 was used as the starting material.en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.subjectkjemien_US
dc.titleSynthesis of an Alleged Byproduct Precursor in Iodixanol Preparationen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2018 American Chemical Societyen_US
dc.subject.nsiVDP::Matematikk og Naturvitenskap: 400::Kjemi: 440en_US
dc.source.pagenumber7344-7349en_US
dc.source.volume3en_US
dc.source.journalACS Omegaen_US
dc.source.issue7en_US
dc.identifier.doi10.1021/acsomega.8b00411
dc.identifier.cristin1596039
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse-Ikkekommersiell 4.0 Internasjonal