Asymmetric Catalytic Synthesis of -Aryl--Hydroxy Esters with Chiral Rhodium-NHC type Catalysts
| dc.contributor.author | Burke, Anthony | |
| dc.contributor.author | Marques, Carolina | |
| dc.contributor.editor | Davies, Stephen | |
| dc.date.accessioned | 2014-01-24T10:23:18Z | |
| dc.date.available | 2014-01-24T10:23:18Z | |
| dc.date.issued | 2013-06-15 | |
| dc.description.abstract | Herein 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.authoremail | ajb@uevora.pt | |
| dc.identifier.authoremail | carolsmarq@gmail.com | |
| dc.identifier.doi | 10.1016/j.tetasy.2013.04.011 | |
| dc.identifier.issn | 0957-4166 | |
| dc.identifier.numrev | 11 | |
| dc.identifier.pagina | 628-632 | |
| dc.identifier.principalpublicationtitle | Enantioselective catalytic synthesis of ethyl mandelate derivatives using Rh(I)-NHC catalysts and organoboron reagents | |
| dc.identifier.revista | Tetrahedron Asymmetry | |
| dc.identifier.scientificarea | 307 | por |
| dc.identifier.uri | http://hdl.handle.net/10174/9968 | |
| dc.identifier.volume | 24 | |
| dc.language.iso | eng | por |
| dc.peerreviewed | yes | por |
| dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD, | por |
| dc.rights | restrictedAccess | por |
| dc.subject | Síntese | por |
| dc.subject | Catálise | por |
| dc.title | Asymmetric Catalytic Synthesis of -Aryl--Hydroxy Esters with Chiral Rhodium-NHC type Catalysts | por |
| dc.type | article | por |