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dc.contributor.authorConnon, Stephenen
dc.date.accessioned2022-12-14T11:17:32Z
dc.date.available2022-12-14T11:17:32Z
dc.date.issued2022en
dc.date.submitted2022en
dc.identifier.citationSmith S.N., Trujillo C., Connon S.J., Catalytic, asymmetric azidations at carbonyls: achiral and meso-anhydride desymmetrisation affords enantioenriched ?-lactams, Organic and Biomolecular Chemistry, 20, 32, 2022, 6384 - 6393, 6384-6393en
dc.identifier.issn14770520en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description10.1039/d2ob01040ben
dc.description.abstractAn unprecedented organocatalytic process involving the asymmetric addition of azide to meso-anhydrides has been developed, promoted by novel sulfamide-substituted Cinchona alkaloid-based catalysts. Readily available glutaric anhydrides can be smoothly converted to enantioenriched hemi-acyl azides and from there to either γ-amino acids or γ-lactams.en
dc.format.extent6384-6393en
dc.format.extent6384en
dc.format.extent6393en
dc.language.isoenen
dc.relation.ispartofseriesOrganic and Biomolecular Chemistryen
dc.relation.ispartofseries20en
dc.relation.ispartofseries32en
dc.rightsYen
dc.subjectazideen
dc.subjectγ-amino acidsen
dc.subjectγ-lactamsen
dc.subjectmeso-anhydridesen
dc.titleCatalytic, asymmetric azidations at carbonyls: achiral and meso-anhydride desymmetrisation affords enantioenriched ?-lactamsen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/connonsen
dc.identifier.rssinternalid249087en
dc.identifier.doihttp://dx.doi.org/10.1039/d2ob01040ben
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0003-2984-9246en
dc.identifier.urihttp://hdl.handle.net/2262/101875


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