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dc.contributor.authorBitai, Jacqueline
dc.contributor.authorWestwood, Matthew
dc.contributor.authorSmith, Andrew D.
dc.date.accessioned2021-03-11T09:30:03Z
dc.date.available2021-03-11T09:30:03Z
dc.date.issued2021-03-01
dc.identifier271671427
dc.identifierca3b90f6-bae8-4279-8ff2-beb758c41df4
dc.identifier85103250097
dc.identifier000632575900001
dc.identifier.citationBitai , J , Westwood , M & Smith , A D 2021 , ' α,β-Unsaturated acyl ammonium species as reactive intermediates in organocatalysis : an update ' , Organic & Biomolecular Chemistry , vol. Advance Article . https://doi.org/10.1039/D0OB02208Jen
dc.identifier.issn1477-0520
dc.identifier.urihttps://hdl.handle.net/10023/21602
dc.descriptionAuthors acknowledge The University of St Andrews (JB) and the EaSICAT Centre for Doctoral Training (MTW) for funding.en
dc.description.abstractα,β-Unsaturated acyl ammonium species are versatile intermediates that have been applied in a variety of transformations including Michael additions, domino reactions and cycloadditions. Many of these transformations are promoted by chiral Lewis base catalysts, enabling the rapid generation of molecular complexity with high stereochemical control. This review highlights recent developments in the generation and application of α,β-unsaturated acyl ammonium intermediates reported since a previous review of this area in 2016. Particular emphasis will be placed on reports providing mechanistic insight into catalytic transformations and observed selectivities. A perspective on current challenges and potential future developments in the field of α,β-unsaturated acyl ammonium catalysis is also provided.
dc.format.extent19
dc.format.extent12306270
dc.language.isoeng
dc.relation.ispartofOrganic & Biomolecular Chemistryen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleα,β-Unsaturated acyl ammonium species as reactive intermediates in organocatalysis : an updateen
dc.typeJournal itemen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doihttps://doi.org/10.1039/D0OB02208J
dc.description.statusPeer revieweden
dc.date.embargoedUntil2021-03-01


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