dc.contributor.author | CONNON, STEPHEN | en |
dc.date.accessioned | 2011-02-18T17:41:03Z | |
dc.date.available | 2011-02-18T17:41:03Z | |
dc.date.issued | 2008 | en |
dc.date.submitted | 2008 | en |
dc.identifier.citation | S. J. Connon, Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts, Chemical Communcations, 2008, 2499-2510 | en |
dc.identifier.other | Y | en |
dc.description | PUBLISHED | en |
dc.description.abstract | Cinchona alkaloid derivatives modified to include a (thio)urea component have emerged in the last three years as readily accessible, robust and tunable bifunctional organocatalysts for a range of synthetically useful transformations. The origins of these catalysts and the major developments in their application in enantioselective synthesis are reviewed | en |
dc.description.sponsorship | Our catalysis work was generously supported by the Irish
Research Council for Science, Engineering and Technology
and Science Foundation Ireland. The assistance of Aldo
Peschiulli in proof-reading the manuscript is gratefully
acknowledged. | en |
dc.format.extent | 2499-2510 | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Chemical Communcations | en |
dc.rights | Y | en |
dc.subject | enantioselective synthesis | en |
dc.subject | Biochemistry | en |
dc.subject | organic catalysts | en |
dc.title | Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/connons | en |
dc.identifier.rssinternalid | 71120 | en |
dc.subject.TCDTheme | Nanoscience & Materials | en |
dc.identifier.rssuri | http://dx.doi.org/10.1039/B719249E | en |
dc.contributor.sponsor | Science Foundation Ireland (SFI) | en |
dc.identifier.uri | http://hdl.handle.net/2262/50689 | |