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dc.contributor.authorMalins, Lara R.
dc.contributor.authorGiltrap, Andrew M.
dc.contributor.authorDowman, Luke J.
dc.contributor.authorPayne, Richard J.
dc.date.accessioned2020-06-19
dc.date.available2020-06-19
dc.date.issued2015-04-10
dc.identifier.urihttps://hdl.handle.net/2123/22625
dc.description.abstractThe efficient synthesis of a β-thiol phenylalanine derivative is described starting from Garner’s aldehyde. The utility of this amino acid in peptide ligation–desulfurization chemistry is described, including the trifluoroethanethiol (TFET)-promoted one-pot assembly of the 62 residue peptide hormone augurin.en
dc.language.isoen_USen
dc.publisherAmerican Chemical Societyen
dc.relationARC FT130100150en
dc.rightsOtheren
dc.subjectAldehydesen
dc.subjectPeptides and proteinsen
dc.subjectMonomersen
dc.subjectChemical synthesisen
dc.subjectLigationen
dc.titleSynthesis of β-Thiol Phenylalanine for Applications in One-Pot Ligation- Desulfurization Chemistryen
dc.typeArticleen
dc.subject.asrcFoR::030599 - Organic Chemistry not elsewhere classifieden
dc.identifier.doi10.1021/acs.orglett.5b00597
dc.type.pubtypeAuthor accepted manuscripten
dc.relation.arcFT130100150
dc.rights.otherThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.5b00597en
usyd.facultySeS faculties schools::Faculty of Scienceen


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