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dc.contributor.advisorConnon, Stephen
dc.contributor.authorPiccinini, Alessandro
dc.date.accessioned2019-11-14T11:44:39Z
dc.date.available2019-11-14T11:44:39Z
dc.date.issued2012
dc.identifier.citationAlessandro Piccinini, 'Studies on the Catalytic Asymmetric Synthesis of Terminal Expoxides from Aldehydes', [thesis], Trinity College (Dublin, Ireland). School of Chemistry, 2012, pp 263
dc.identifier.otherTHESIS 9631
dc.description.abstractChiral non racemic terminal epoxides are among most the valuable building blocks available to an organic chemist. The Johnson-Corey-Chaykovksy epoxidation (JCC) of carbonyl compounds is a promising and complementary approach to the classic olefin oxidation methodologies. It represents an efficient and straightforward method for the synthesis of epoxides. However, the JCC enantioselective methylene transfer epoxidation benchmark literature protocols for the synthesis of optically active terminal epoxides are characterised by moderate product yields/enantioselectivity and the requirement for (super)stoichiometric catalyst loadings.
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__Rb15124931
dc.subjectChemistry, Ph.D.
dc.subjectPh.D. Trinity College Dublin.
dc.titleStudies on the Catalytic Asymmetric Synthesis of Terminal Expoxides from Aldehydes
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 263
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/2262/90535


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