Asymmetric Catalytic Synthesis of -Aryl--Hydroxy Esters with Chiral Rhodium-NHC type Catalysts

dc.contributor.authorBurke, Anthony
dc.contributor.authorMarques, Carolina
dc.contributor.editorDavies, Stephen
dc.date.accessioned2014-01-24T10:23:18Z
dc.date.available2014-01-24T10:23:18Z
dc.date.issued2013-06-15
dc.description.abstractHerein we describe for the first time the enantioselective catalytic arylation of ethyl glyoxalate using phenylboron reagents and chiral rhodium(I)-NHC catalysts. (KOBu)-Bu-t was the base of choice, along with tert-amyl alcohol as the solvent. A novel chiral bis-imidazolium salt was synthesized and evaluated for the first time in this catalytic transformation. Although moderate enantioselectivities (up to 34% ee) were obtained for the phenylation reaction, despite the excellent yields, very low enantioselectivities were obtained using other arylboronic acids with a variety of chiral rhodium(I)-NHC catalysts.por
dc.identifier.authoremailajb@uevora.pt
dc.identifier.authoremailcarolsmarq@gmail.com
dc.identifier.doi10.1016/j.tetasy.2013.04.011
dc.identifier.issn0957-4166
dc.identifier.numrev11
dc.identifier.pagina628-632
dc.identifier.principalpublicationtitleEnantioselective catalytic synthesis of ethyl mandelate derivatives using Rh(I)-NHC catalysts and organoboron reagents
dc.identifier.revistaTetrahedron Asymmetry
dc.identifier.scientificarea307por
dc.identifier.urihttp://hdl.handle.net/10174/9968
dc.identifier.volume24
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD,por
dc.rightsrestrictedAccesspor
dc.subjectSíntesepor
dc.subjectCatálisepor
dc.titleAsymmetric Catalytic Synthesis of -Aryl--Hydroxy Esters with Chiral Rhodium-NHC type Catalystspor
dc.typearticlepor

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