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Nickel-catalysed carboxylation of organoboronates

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dc.contributor.authorMakida, Yusuke
dc.contributor.authorMarelli, Enrico
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorNolan, Steven P.
dc.date.accessioned2014-08-18T15:31:06Z
dc.date.available2014-08-18T15:31:06Z
dc.date.issued2014-06-05
dc.identifier.citationMakida , Y , Marelli , E , Slawin , A M Z & Nolan , S P 2014 , ' Nickel-catalysed carboxylation of organoboronates ' , Chemical Communications , vol. 50 , no. 59 , pp. 8010-8013 . https://doi.org/10.1039/C4CC03650Fen
dc.identifier.issn1359-7345
dc.identifier.otherPURE: 141290014
dc.identifier.otherPURE UUID: 7cfc3d40-2c45-41a3-bb8d-39e1b6e2bf28
dc.identifier.otherRIS: urn:937C182E609D00C24D1CDB916B2D72FB
dc.identifier.otherScopus: 84903522733
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861891
dc.identifier.otherWOS: 000338439700023
dc.identifier.urihttps://hdl.handle.net/10023/5190
dc.descriptionThe authors acknowledge the ERC (Advanced Researcher award-FUNCAT, CO2Chem) and King Saud University for funding and the EPSRC NMSSC in Swansea for mass spectrometric analyses. SPN is a Royal Society Wolfson Research Merit Award holder.en
dc.description.abstractA nickel/N-heterocyclic carbene (NHC) catalysed carboxylation of aryl-, heteroaryl- and alkenylboronates, affording the corresponding carboxylic acids, has been developed. This transformation proceeds under one atmosphere of CO2 with a broad range of substrates and exhibits good functional group compatibility.
dc.format.extent4
dc.language.isoeng
dc.relation.ispartofChemical Communicationsen
dc.rights© Royal Society of Chemistry 2014. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (http://creativecommons.org/licenses/by/3.0/).en
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleNickel-catalysed carboxylation of organoboronatesen
dc.typeJournal articleen
dc.contributor.sponsorEuropean Research Councilen
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/10.1039/C4CC03650F
dc.description.statusPeer revieweden
dc.identifier.urlhttp://www.rsc.org/suppdata/cc/c4/c4cc03650f/c4cc03650f1.pdfen
dc.identifier.urlhttp://www.rsc.org/suppdata/cc/c4/c4cc03650f/c4cc03650f2.cifen
dc.identifier.grantnumberFP7-227817 FUNCATen


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