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dc.contributor.advisorBergin, Enda
dc.contributor.authorFrauenlob, Robin
dc.date.accessioned2019-11-06T11:22:32Z
dc.date.available2019-11-06T11:22:32Z
dc.date.issued2013
dc.identifier.citationRobin Frauenlob, 'New methodologies for catalysis and combinatorial chemistry', [thesis], Trinity College (Dublin, Ireland). School of Chemistry, 2013, pp 206
dc.identifier.otherTHESIS 9846
dc.description.abstractThe enantioselective synthesis of chiral molecules, such as those required by the pharmaceutical industry, is one of the most important tasks in chemistry. Asymmetric catalysis is an attractive way to synthesise enantiopure compounds. Thus, the synthesis of chiral ligands has shown a great interest. Catalytic methods for the generation of enantiomerically pure compounds traditionally can be a difficult and time consuming process. The selectivity of a reaction depends not only on the catalyst but also on the substrate, which makes the quest of finding a catalyst for a specific substrate harder.
dc.format1 volume
dc.language.isoen
dc.publisherTrinity College (Dublin, Ireland). School of Chemistry
dc.relation.isversionofhttp://stella.catalogue.tcd.ie/iii/encore/record/C__Rb15319146
dc.subjectChemistry, Ph.D.
dc.subjectPh.D. Trinity College Dublin.
dc.titleNew methodologies for catalysis and combinatorial chemistry
dc.typethesis
dc.type.supercollectionthesis_dissertations
dc.type.supercollectionrefereed_publications
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (Ph.D.)
dc.rights.ecaccessrightsopenAccess
dc.format.extentpaginationpp 206
dc.description.noteTARA (Trinity’s Access to Research Archive) has a robust takedown policy. Please contact us if you have any concerns: rssadmin@tcd.ie
dc.identifier.urihttp://hdl.handle.net/2262/90159


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