Show simple item record

Files in this item

Thumbnail
Name:
Harkness_2017_EJOC_ConciseSynthesis_AAM.pdf
Size:
1.654Mb
Format:
PDF
View/Open

A highly enantioselective alkene methoxycarbonylation enables a concise synthesis of (S)-flurbiprofen

Item metadata

dc.contributor.authorHarkness, Gavin J.
dc.contributor.authorClarke, Matthew Lee
dc.date.accessioned2018-08-31T08:35:20Z
dc.date.available2018-08-31T08:35:20Z
dc.date.issued2017-09-01
dc.identifier250595953
dc.identifier491c2b82-8919-4b89-886d-09e22624b8c7
dc.identifier85028616589
dc.identifier000408853700026
dc.identifier.citationHarkness , G J & Clarke , M L 2017 , ' A highly enantioselective alkene methoxycarbonylation enables a concise synthesis of (S)-flurbiprofen ' , European Journal of Organic Chemistry , vol. 2017 , no. 32 , pp. 4859-4863 . https://doi.org/10.1002/ejoc.201700791en
dc.identifier.issn1099-0690
dc.identifier.otherBibtex: urn:435df28e3f9b0a525fe2f482fc830de9
dc.identifier.otherORCID: /0000-0002-2444-1244/work/59464627
dc.identifier.urihttps://hdl.handle.net/10023/15914
dc.descriptionThe authors thank the EPSRC for funding for this programme from EP/MC038868/1 and via the DTG.en
dc.description.abstractA highly enantioselective synthesis of (S)-Flurbiprofen methyl ester in two steps from commercially available 4-bromo-2-fluoro-1,1'-biphenyl is shown. [PdCl2((S)-Xylyl-Phanephos)] catalyst is used to accomplish both Grignard cross-coupling and the highly enantioselective intermolecular methoxycarbonylation reaction.
dc.format.extent5
dc.format.extent1734659
dc.language.isoeng
dc.relation.ispartofEuropean Journal of Organic Chemistryen
dc.subjectPalladiumen
dc.subjectAsymmetric catalysisen
dc.subjectCarbonylationen
dc.subjectHydroesterificationen
dc.subjectHydroxycarbonylationen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleA highly enantioselective alkene methoxycarbonylation enables a concise synthesis of (S)-flurbiprofenen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1002/ejoc.201700791
dc.description.statusPeer revieweden
dc.date.embargoedUntil2018-08-31
dc.identifier.grantnumberEP/M003868/1en


This item appears in the following Collection(s)

Show simple item record

Items in the St Andrews Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.