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dc.contributor.authorFuentes García, José Antonio
dc.contributor.authorCarpenter, Ian
dc.contributor.authorKann, Nina
dc.contributor.authorClarke, Matt
dc.date.accessioned2013-10-24T10:01:04Z
dc.date.available2013-10-24T10:01:04Z
dc.date.issued2013-09
dc.identifier.citationFuentes García , J A , Carpenter , I , Kann , N & Clarke , M 2013 , ' Highly enantioselective hydrogenation and transfer hydrogenation of cycloalkyl and heterocyclic ketones catalysed by an iridium complex of a tridentate phosphine-diamine ligand ' , Chemical Communications , vol. 49 , no. 87 , pp. 10245-10247 . https://doi.org/10.1039/C3CC45545Aen
dc.identifier.issn1359-7345
dc.identifier.otherPURE: 76089556
dc.identifier.otherPURE UUID: e2113761-fbfb-433c-ab3e-9f4896e80e79
dc.identifier.otherScopus: 84885391480
dc.identifier.otherORCID: /0000-0002-2444-1244/work/59464604
dc.identifier.urihttps://hdl.handle.net/10023/4116
dc.description.abstractIr complexes of chiral phosphine-diamine ligands catalyse the hydrogenation and transfer hydrogenation of aryl-piperidin-4-yl methanones, and ketones bearing both an aryl group and secondary alkyl substituent with up to 98% e.e., and with substrate to catalyst ratios of up to 4000.
dc.language.isoeng
dc.relation.ispartofChemical Communicationsen
dc.rightsCopyright 2013, the Authors. This is an Open Access article licensed under a Creative Commons Attribution 3.0 Unported Licence.en
dc.subjectIridium complexen
dc.subjectEnantioselective hydrogenationen
dc.subjectTransfer hydrogenationen
dc.subjectHeterocyclic ketonesen
dc.subjectCycloalkyl ketonesen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleHighly enantioselective hydrogenation and transfer hydrogenation of cycloalkyl and heterocyclic ketones catalysed by an iridium complex of a tridentate phosphine-diamine liganden
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1039/C3CC45545A
dc.description.statusPeer revieweden


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