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dc.contributor.authorCONNON, STEPHENen
dc.date.accessioned2011-02-15T16:28:35Z
dc.date.available2011-02-15T16:28:35Z
dc.date.issued2009en
dc.date.submitted2009en
dc.identifier.citationS. E. O Toole and S. J. Connon, The enantioselective benzoin condensation promoted by chiral triazolium precatalysts: stereochemical control via hydrogen bonding., Organic Biomolecular Chemistry, 7, 17, 2009, 3584-3593en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.descriptionPMID: 19675916en
dc.description.abstractThe design of a new class of triazolium ion precatalysts incorporating protic substituents is described. These materials promote the enantioselective benzoin condensation of a range of aromatic aldehydes (1?62% ee). Catalyst evaluation studies strongly support the involvement of hydrogen bond donation by the catalyst in the stereocentre-forming step of the catalytic cycle.en
dc.description.sponsorshipFinancial support from Science Foundation Ireland (SFI) and Trinity College is gratefully acknowledged.en
dc.format.extent3584-3593en
dc.language.isoenen
dc.relation.ispartofseriesOrganic Biomolecular Chemistryen
dc.relation.ispartofseries7en
dc.relation.ispartofseries17en
dc.rightsYen
dc.subjectOrganic chemistryen
dc.subjecthydrogen bondingen
dc.titleThe enantioselective benzoin condensation promoted by chiral triazolium precatalysts: stereochemical control via hydrogen bonding.en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/connonsen
dc.identifier.rssinternalid71072en
dc.subject.TCDThemeNanoscience & Materialsen
dc.identifier.rssurihttp://dx.doi.org/10.1039/B908517Cen
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.identifier.urihttp://hdl.handle.net/2262/50583


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