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dc.contributor.authorTrose, Michael
dc.contributor.authorLazreg, Faima
dc.contributor.authorLesieur, Mathieu
dc.contributor.authorCazin, Catherine S.J.
dc.date.accessioned2016-10-01T23:39:41Z
dc.date.available2016-10-01T23:39:41Z
dc.date.issued2015
dc.identifier.citationTrose , M , Lazreg , F , Lesieur , M & Cazin , C S J 2015 , ' Copper N -heterocyclic carbene complexes as active catalysts for the synthesis of 2-substituted oxazolines from nitriles and aminoalcohols ' , The Journal of Organic Chemistry , vol. Article ASAP . https://doi.org/10.1021/acs.joc.5b01382en
dc.identifier.issn0022-3263
dc.identifier.otherPURE: 218885672
dc.identifier.otherPURE UUID: 12cb9e58-66b6-4f01-9dfb-e647d3b8ee3b
dc.identifier.otherScopus: 84944937175
dc.identifier.otherWOS: 000363224600011
dc.identifier.urihttps://hdl.handle.net/10023/9588
dc.descriptionThe authors gratefully acknowledge the Royal Society (University research Fellowship to C.S.J.C) for funding.en
dc.description.abstractThe reaction between nitriles and aminoalcohols to access 2-substituted oxazolines was investigated. Using copper–NHC complexes, various nitriles were successfully converted into the corresponding oxazolines, under milder and less wasteful conditions than previously reported methods.
dc.language.isoeng
dc.relation.ispartofThe Journal of Organic Chemistryen
dc.rights© 2015 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Organic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://dx.doi.org/10.1021/acs.joc.5b01382en
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleCopper N-heterocyclic carbene complexes as active catalysts for the synthesis of 2-substituted oxazolines from nitriles and aminoalcoholsen
dc.typeJournal articleen
dc.contributor.sponsorThe Royal Societyen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1021/acs.joc.5b01382
dc.description.statusPeer revieweden
dc.date.embargoedUntil2016-10-01
dc.identifier.urlhttp://pubs.acs.org/doi/suppl/10.1021/acs.joc.5b01382qen
dc.identifier.grantnumberUF100691en


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