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dc.contributor.authorMakida, Yusuke
dc.contributor.authorMarelli, Enrico
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorNolan, Steven P.
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 .
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.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.relation.ispartofChemical Communicationsen
dc.rights© Royal Society of Chemistry 2014. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (
dc.subjectQD Chemistryen
dc.titleNickel-catalysed carboxylation of organoboronatesen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.description.statusPeer revieweden

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