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dc.contributor.authorAyoup , Mohammed Salah
dc.contributor.authorCordes, David Bradford
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.contributor.authorO'Hagan, David
dc.date.accessioned2016-04-15T15:52:08Z
dc.date.available2016-04-15T15:52:08Z
dc.date.issued2015-05-28
dc.identifier181272011
dc.identifier0f4d008e-57c2-4d13-b9b8-5f3e00ada914
dc.identifier84929376570
dc.identifier000354438400009
dc.identifier.citationAyoup , M S , Cordes , D B , Slawin , A M Z & O'Hagan , D 2015 , ' Fluorine containing amino acids : synthesis and peptide coupling of amino acids containing the all-cis tetrafluorocyclohexyl motif ' , Organic & Biomolecular Chemistry , vol. 13 , no. 20 , pp. 5621-5624 . https://doi.org/10.1039/C5OB00650Cen
dc.identifier.issn1477-0520
dc.identifier.otherORCID: /0000-0002-5366-9168/work/28024000
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861404
dc.identifier.otherORCID: /0000-0002-0510-5552/work/68281212
dc.identifier.urihttps://hdl.handle.net/10023/8616
dc.descriptionMA thanks the Egyptian Government for a Scholarship. DO’H thanks the Royal Society for a Royal Society Wolfson Research Merit Award.en
dc.description.abstractA synthesis of two (S)-phenylalanine derivatives is described which have the all-cis, 2,3,5,6-tetrafluorocyclohexyl motif attached to the aromatic ring at the meta and para positions; the para substituted isomer is elaborated into illustrative dipeptides via the free amine and carboxylate respectively demonstrating its utility as a novel amino acid for peptide synthesis and offering a vehicle for incorporation of this unique and facially polarized ring system into bioactive compounds.
dc.format.extent214800
dc.language.isoeng
dc.relation.ispartofOrganic & Biomolecular Chemistryen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleFluorine containing amino acids : synthesis and peptide coupling of amino acids containing the all-cis tetrafluorocyclohexyl motifen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
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.doi10.1039/C5OB00650C
dc.description.statusPeer revieweden
dc.date.embargoedUntil2016-04-15
dc.identifier.grantnumberEP/K031252/1en
dc.identifier.grantnumberEP/K039210/1en


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