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Chiral carbonyl hypoiodites

dc.contributor.authorMattila, Milla
dc.contributor.authorRissanen, Kari
dc.contributor.authorWard, Jas S.
dc.date.accessioned2023-04-03T06:08:03Z
dc.date.available2023-04-03T06:08:03Z
dc.date.issued2023
dc.identifier.citationMattila, M., Rissanen, K., & Ward, J. S. (2023). Chiral carbonyl hypoiodites. <i>Chemical Communications</i>, <i>59</i>(31), 4648-4651. <a href="https://doi.org/10.1039/d3cc00259d" target="_blank">https://doi.org/10.1039/d3cc00259d</a>
dc.identifier.otherCONVID_182526304
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/86228
dc.description.abstractThree chiral carbonyl hypoiodites, R–C(O)OI, have been prepared from N-protected (S)-valine to give the ligand-stabilised (S)-valinoyl hypoiodite complexes with 4-dimethylaminopyridine, 4-pyrrolidinopyridine, and 4-morpholinopyridine as the stabilising ligands. The identity of the complexes was established by NMR (1H, 13C, 1H–15N HMBC) and single crystal X-ray diffraction analysis.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.ispartofseriesChemical Communications
dc.rightsCC BY 4.0
dc.titleChiral carbonyl hypoiodites
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202304032363
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange4648-4651
dc.relation.issn1359-7345
dc.relation.numberinseries31
dc.relation.volume59
dc.type.versionpublishedVersion
dc.rights.copyright© Authors 2023
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber351121
dc.relation.grantnumber356187
dc.subject.ysokarbonyylit
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p14898
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1039/d3cc00259d
dc.relation.funderResearch Council of Finlanden
dc.relation.funderResearch Council of Finlanden
dc.relation.funderSuomen Akatemiafi
dc.relation.funderSuomen Akatemiafi
jyx.fundingprogramAcademy Project, AoFen
jyx.fundingprogramAcademy Research Fellow, AoFen
jyx.fundingprogramAkatemiahanke, SAfi
jyx.fundingprogramAkatemiatutkija, SAfi
jyx.fundinginformationThe authors gratefully acknowledge the Academy of Finland (K.R. grant No. 351121), the Magnus Ehrnrooth Foundation (J.S.W.), and the University of Jyväskylä, Finland for financial support.
dc.type.okmA1


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