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dc.contributor.authorCONNON, STEPHENen
dc.date.accessioned2011-02-18T17:41:03Z
dc.date.available2011-02-18T17:41:03Z
dc.date.issued2008en
dc.date.submitted2008en
dc.identifier.citationS. J. Connon, Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts, Chemical Communcations, 2008, 2499-2510en
dc.identifier.otherYen
dc.identifier.urihttp://hdl.handle.net/2262/50689
dc.descriptionPUBLISHEDen
dc.description.abstractCinchona 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 revieweden
dc.description.sponsorshipOur 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.extent2499-2510en
dc.language.isoenen
dc.relation.ispartofseriesChemical Communcationsen
dc.rightsYen
dc.subjectenantioselective synthesisen
dc.subjectBiochemistryen
dc.subjectorganic catalystsen
dc.titleAsymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalystsen
dc.typeJournal Articleen
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/connonsen
dc.identifier.rssinternalid71120en
dc.subject.TCDThemeNanoscience & Materialsen
dc.identifier.rssurihttp://dx.doi.org/10.1039/B719249Een


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