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dc.contributor.authorMcErlain, Holly
dc.contributor.authorAndrews, Matthew J.
dc.contributor.authorWatson, Allan J. B.
dc.contributor.authorPimlott, Sally L.
dc.contributor.authorSutherland, Andrew
dc.date.accessioned2024-02-19T12:30:17Z
dc.date.available2024-02-19T12:30:17Z
dc.date.issued2024-02-09
dc.identifier299396380
dc.identifier68c84206-1f4f-4539-8653-665888aa4a8b
dc.identifier85185832159
dc.identifier.citationMcErlain , H , Andrews , M J , Watson , A J B , Pimlott , S L & Sutherland , A 2024 , ' Ligand-enabled copper-mediated radioiodination of arenes ' , Organic Letters , vol. Ahead of Print . https://doi.org/10.1021/acs.orglett.4c00356en
dc.identifier.issn1523-7060
dc.identifier.otherJisc: 1765652
dc.identifier.otherORCID: /0000-0002-1582-4286/work/153977707
dc.identifier.urihttps://hdl.handle.net/10023/29289
dc.description.abstractThe discovery of a copper precatalyst that facilitates the key mechanistic steps of arene halodeboronation has allowed a step change in the synthesis of radioiodine-containing arenes. The active precatalyst [Cu(OAc)(phen)2]OAc was shown to perform room temperature radio-iododeboronation of aryl boronic acids with 1–2 mol % loadings and 10 min reaction times. These mild conditions enable particularly clean reactions, as demonstrated with the efficient preparation of the radiopharmaceutical and SPECT tracer, meta-iodobenzylguanidine (MIBG).
dc.format.extent5
dc.format.extent1552444
dc.language.isoeng
dc.relation.ispartofOrganic Lettersen
dc.subjectQD Chemistryen
dc.subjectATC-NDASen
dc.subject.lccQDen
dc.titleLigand-enabled copper-mediated radioiodination of arenesen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorThe Leverhulme Trusten
dc.contributor.sponsorUK Research and Innovationen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Sir James Mackenzie Institute for Early Diagnosisen
dc.identifier.doi10.1021/acs.orglett.4c00356
dc.description.statusPeer revieweden
dc.identifier.grantnumberEP/S027165/1en
dc.identifier.grantnumberRF-2022-014en
dc.identifier.grantnumberEP/W007517/1en


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