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dc.contributor.authorKeddie, Neil S.
dc.contributor.authorChampagne, Pier Alexandre
dc.contributor.authorDesroches, Justine
dc.contributor.authorPaquin, Jean-Francois
dc.contributor.authorO'Hagan, David
dc.date.accessioned2018-02-05T12:30:09Z
dc.date.available2018-02-05T12:30:09Z
dc.date.issued2018-01-09
dc.identifier.citationKeddie , N S , Champagne , P A , Desroches , J , Paquin , J-F & O'Hagan , D 2018 , ' Stereochemical outcomes of C-F activation reactions of benzyl fluoride ' , Beilstein Journal of Organic Chemistry , vol. 14 , pp. 106-113 . https://doi.org/10.3762/bjoc.14.6en
dc.identifier.issn1860-5397
dc.identifier.otherPURE: 252181382
dc.identifier.otherPURE UUID: db10989b-2ae7-4ea4-9f30-79db0bb8e5ea
dc.identifier.otherWOS: 000423182500001
dc.identifier.otherScopus: 85041060552
dc.identifier.otherORCID: /0000-0002-9502-5862/work/57821654
dc.identifier.otherWOS: 000423182500001
dc.identifier.otherORCID: /0000-0002-0510-5552/work/68281202
dc.identifier.urihttp://hdl.handle.net/10023/12668
dc.descriptionNK and DOH acknowledge support from the University of St Andrews, Engineering and Physical Sciences Research Council (EPSRC, Grant No.: EP/L017911/1), and the EPSRC UK National Mass Spectrometry Facility at Swansea University. This work was also supported by the Natural Sciences and Engineering Research Council of Canada (NSERC), the FRQNT Centre in Green Chemistry and Catalysis (CGCC), and the Université Laval.en
dc.description.abstractIn recent years, the highly polar C-F bond has been utilised in activation chemistry despite its low reactivity to traditional nucleophiles, when compared to other C-X halogen bonds. Paquin's group has reported extensive studies on the C-F activation of benzylic fluorides for nucleophilic substitutions and Friedel-Crafts reactions, using a range of hydrogen bond donors such as water, triols or hexafluoroisopropanol (HFIP) as the activators. This study examines the stereointegrity of the C-F activation reaction through the use of an enantiopure isotopomer of benzyl fluoride to identify whether the reaction conditions favour a dissociative (SN1) or associative (SN2) pathway. [2H]-Isotopomer ratios in the reactions were assayed using the Courtieu 2H NMR method in a chiral liquid crystal (poly-γ-benzyl-L-glutamate) matrix and demonstrated that both associative and dissociative pathways operate to varying degrees, according to the nature of the nucleophile and the hydrogen bond donor.
dc.format.extent8
dc.language.isoeng
dc.relation.ispartofBeilstein Journal of Organic Chemistryen
dc.rights© 2018 Keddie 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.subjectBenzylic fluoridesen
dc.subjectC-F activationen
dc.subjectChiral liquid crystalen
dc.subject2H NMRen
dc.subjectPBLGen
dc.subjectstereochemistryen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleStereochemical outcomes of C-F activation reactions of benzyl fluorideen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews.Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.3762/bjoc.14.6
dc.description.statusPeer revieweden


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