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A new synthetic route to p-methoxy-2,6-disubstituted anilines and their conversion into N-heterocyclic carbene precursors

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dc.contributor.authorMeiries, Sebastien Michel Bernard
dc.contributor.authorNolan, Steven Patrick
dc.date.accessioned2014-12-03T00:01:26Z
dc.date.available2014-12-03T00:01:26Z
dc.date.issued2014
dc.identifier.citationMeiries , S M B & Nolan , S P 2014 , ' A new synthetic route to p -methoxy-2,6-disubstituted anilines and their conversion into N-heterocyclic carbene precursors ' , Synlett , vol. 25 , no. 3 , pp. 393-398 . https://doi.org/10.1055/s-0033-1340105en
dc.identifier.issn0936-5214
dc.identifier.otherPURE: 118744863
dc.identifier.otherPURE UUID: d18c0a32-08c7-4573-8fdd-7f33e6274cba
dc.identifier.otherScopus: 84893779664
dc.identifier.otherWOS: 000331220800016
dc.identifier.urihttps://hdl.handle.net/10023/5858
dc.description.abstractThe development of new N-heterocyclic carbenes (NHC) is a key feature in this now mainstream research area to access novel chemical properties and reactivity that are essential for the discovery of original applications. Up to now, only a few reliable methods have proven suitable for the preparation of methoxylated anilines to ultimately access methoxylated NHC. We are pleased to report here a straightforward and scalable approach to address this matter.
dc.format.extent6
dc.language.isoeng
dc.relation.ispartofSynletten
dc.rights© Georg Thieme Verlag Stuttgart · New Yorken
dc.subjectLigandsen
dc.subjectNucleophilic aromaticen
dc.subjectCopperen
dc.subjectCatalysisen
dc.subjectCarbenesen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleA new synthetic route to p-methoxy-2,6-disubstituted anilines and their conversion into N-heterocyclic carbene precursorsen
dc.typeJournal itemen
dc.contributor.sponsorThe Royal Societyen
dc.contributor.sponsorEuropean Research Councilen
dc.contributor.sponsorEuropean Commissionen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1055/s-0033-1340105
dc.description.statusPeer revieweden
dc.date.embargoedUntil2014-12-03
dc.identifier.grantnumberWM100010en
dc.identifier.grantnumberFP7-227817 FUNCATen
dc.identifier.grantnumber246461en


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