| dc.contributor.advisor | Connon, Stephen | |
| dc.contributor.author | Procuranti, Barbara | |
| dc.date.accessioned | 2019-11-14T12:05:25Z | |
| dc.date.available | 2019-11-14T12:05:25Z | |
| dc.date.issued | 2010 | |
| dc.identifier.citation | Barbara Procuranti, 'Studies on the design of novel organocatalysts for reduction, carbonyl protection and asymmetric acylation reactions', [thesis], Trinity College (Dublin, Ireland). School of Chemistry, 2010, pp 218 | |
| dc.identifier.other | THESIS 9017 | |
| dc.description.abstract | Due to the vast number of biologically active compounds bearing a hydrogen substituent as a part of the stereogenic center, the development of efficient reduction reactions has been a main focus within the area of asymmetric catalysis. Herein we detail the design and synthesis of chiral (metal-free) bifunctional organocatalysts, specifically inexpensive and easily assembled (thio)urea derivatives, for enantioselective reduction of benzils to benzoins. | |
| dc.format | 1 volume | |
| dc.language.iso | en | |
| dc.publisher | Trinity College (Dublin, Ireland). School of Chemistry | |
| dc.relation.isversionof | http://stella.catalogue.tcd.ie/iii/encore/record/C__Rb14615716 | |
| dc.subject | Chemistry, Ph.D. | |
| dc.subject | Ph.D. Trinity College Dublin. | |
| dc.title | Studies on the design of novel organocatalysts for reduction, carbonyl protection and asymmetric acylation reactions | |
| dc.type | thesis | |
| dc.type.supercollection | thesis_dissertations | |
| dc.type.supercollection | refereed_publications | |
| dc.type.qualificationlevel | Doctoral | |
| dc.type.qualificationname | Doctor of Philosophy (Ph.D.) | |
| dc.rights.ecaccessrights | openAccess | |
| dc.format.extentpagination | pp 218 | |
| dc.description.note | TARA (Trinity’s Access to Research Archive) has a robust takedown policy. Please contact us if you have any concerns: rssadmin@tcd.ie | |
| dc.identifier.uri | http://hdl.handle.net/2262/90547 | |
