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dc.contributor.authorQuerard, Pierre
dc.contributor.authorPerepichka, Inna
dc.contributor.authorZysman-Colman, Eli
dc.contributor.authorLi, Chao-Jun
dc.date.accessioned2017-01-13T15:30:11Z
dc.date.available2017-01-13T15:30:11Z
dc.date.issued2016-12-06
dc.identifier.citationQuerard , P , Perepichka , I , Zysman-Colman , E & Li , C-J 2016 , ' Copper-catalyzed asymmetric sp 3 C-H arylation of tetrahydroisoquinoline mediated by a visible light photoredox catalyst ' , Beilstein Journal of Organic Chemistry , vol. 12 , pp. 2636-2643 . https://doi.org/10.3762/bjoc.12.260en
dc.identifier.issn1860-5397
dc.identifier.otherPURE: 248878156
dc.identifier.otherPURE UUID: 262749ae-f868-4ee1-97c8-106ba91655df
dc.identifier.otherScopus: 85008153150
dc.identifier.otherORCID: /0000-0001-7183-6022/work/56639095
dc.identifier.otherWOS: 000391505400002
dc.identifier.urihttps://hdl.handle.net/10023/10099
dc.descriptionWe are grateful to the Canada Research Chair (Tier 1) foundation (to C.-J. Li), NSERC, CFI, and FQRNT (CCVC) for their support of our research.en
dc.description.abstractThis report describes a highly enantioselective oxidative sp3 C-H arylation of N-aryltetrahydroisoquinolines (THIQs) through a dual catalysis platform. The combination of the photoredox catalyst, [Ir(ppy)2(dtbbpy)]PF6, and chiral copper catalysts provide a mild and highly effective sp3 C-H asymmetric arylation of THIQs.
dc.format.extent8
dc.language.isoeng
dc.relation.ispartofBeilstein Journal of Organic Chemistryen
dc.rights© 2016 Querard et al.; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.subjectC-H arylationen
dc.subjectCopper catalysten
dc.subjectEnantioselectivityen
dc.subjectVisible lighten
dc.subjectQD Chemistryen
dc.subjectOrganic Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleCopper-catalyzed asymmetric sp3 C-H arylation of tetrahydroisoquinoline mediated by a visible light photoredox catalysten
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. Organic Semiconductor Centreen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.3762/bjoc.12.260
dc.description.statusPeer revieweden


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