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Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates

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dc.contributor.authorMorrill, Louis C.
dc.contributor.authorSmith, Andrew D.
dc.date.accessioned2015-02-04T09:31:10Z
dc.date.available2015-02-04T09:31:10Z
dc.date.issued2014-09-07
dc.identifier.citationMorrill , L C & Smith , A D 2014 , ' Organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolates ' , Chemical Society Reviews , vol. 43 , no. 17 , pp. 6214-6226 . https://doi.org/10.1039/c4cs00042ken
dc.identifier.issn0306-0012
dc.identifier.otherPURE: 159426003
dc.identifier.otherPURE UUID: c0621c60-db72-4edd-8df9-9ec1e0c52c10
dc.identifier.otherWOS: 000340705900003
dc.identifier.otherScopus: 84905280739
dc.identifier.otherWOS: 000340705900003
dc.identifier.urihttps://hdl.handle.net/10023/6065
dc.description.abstractThis tutorial review highlights the organocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium/azolium enolates. The generation and synthetic utility of these powerful intermediates is highlighted through their application in various methodologies including aldol-lactonisations, Michael-lactonisations/lactamisations and [2,3]-rearrangements.
dc.format.extent13
dc.language.isoeng
dc.relation.ispartofChemical Society Reviewsen
dc.rights© The Authors 2014. This Open Access Article is licensed under a Creative Commons Attribution 3.0 Unported Licence (http://creativecommons.org/licenses/by/3.0/)en
dc.subjectBicyclic-Beta-Lactonesen
dc.subjectCatalyzed Aldol-Lactonizationen
dc.subjectPromoted Bis-Cyclizationsen
dc.subjectOne-Pot Synthesisen
dc.subjectAsymmetric-Synthesisen
dc.subjectDyotropic Rearrangementsen
dc.subjectNcal Reactionsen
dc.subjectKeto Acidsen
dc.subjectActivationen
dc.subjectDerivativesen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleOrganocatalytic Lewis base functionalisation of carboxylic acids, esters and anhydrides via C1-ammonium or azolium enolatesen
dc.typeJournal itemen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1039/c4cs00042k
dc.description.statusPeer revieweden


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