Show simple item record

Files in this item

Thumbnail

Item metadata

dc.contributor.advisorSmith, Andrew David
dc.contributor.authorRobinson, Emily R. T.
dc.coverage.spatialxiii, 223 p.en_US
dc.date.accessioned2015-07-22T09:33:17Z
dc.date.available2015-07-22T09:33:17Z
dc.date.issued2015-11-30
dc.identifier.urihttp://hdl.handle.net/10023/7010
dc.description.abstractThis thesis details investigations into the generation and synthetic utility of α,β-unsaturated acyl ammonium intermediates using isothioureas as Lewis base organocatalysts to generate a range of heterocyclic products. Initial investigations focussed on the development of a Michael addition-lactonisation protocol utilising α,β-unsaturated acyl ammonium intermediates (generated in situ from HBTM 2.1 and α,β-unsaturated homoanhydrides) and a range of 1,3-dicarbonyl nucleophiles. Products could be isolated as lactones or as ring-opened highly functionalised esters, giving good yields and excellent enantioselectivity. 1,3-Diketones were shown to generate a mixture of regioisomers and whereas 1,3-ketoesters afforded only a single regioisomer. A crystal structure of an α,β-unsaturated acyl ammonium intermediate was obtained that clearly demonstrated steric blocking of the Si- face of the alkene by the catalyst stereodirecting groups, therefore it can be postulated that enantiocontrol in the addition occurs by selective nucleophilic addition from the Re- face. α,β-Unsaturated acyl ammonium species were then shown to participate in asymmetric annulation processes with benzazole nucleophiles to afford highly functionalised heterocyclic products, with both lactone and lactam formation observed. The relationship between nucleophile structure and process regioselectivity was investigated and it was demonstrated that benzothiazole and benzimidazole nucleophiles afforded preferential N-cyclisation to give lactams whilst benzoxazoles exhibited O-cyclisation to form lactones. It was also possible to influence the regioselectivity by changing the electronic properties of the acyl group (R’). Due to the reactivity of this class of nucleophiles it was possible to access products with quaternary centres. Palladium-catalysed cross coupling reactions were also successful on 3-bromo substituted lactams, demonstrating the potential for further derivatising these interesting heterocyclic products. Finally, a cascade protocol was developed that employed Michael-Michael-lactonisation steps to give tricyclic products from enone malonate nucleophiles and α,β-unsaturated acyl ammonium intermediates (generated in situ by addition of HBTM 2.1 into acid chlorides). Interestingly, the reaction showed higher enantioselectivity at elevated temperatures (70 ˚C) and moderate regioselectivity (1,4- vs. 1,2-addition), which could not be improved after extensive screening. A range of lactones was isolated in moderate yields and enantioselectivity.en_US
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.subjectOrganocatalysisen_US
dc.subjectCatalysisen_US
dc.subjectMichael additionen_US
dc.subjectAsymmetricen_US
dc.subjectα,β-unsaturated acyl ammoniumen_US
dc.subject.lccQD505.R74
dc.subject.lcshCatalysisen_US
dc.subject.lcshAsymmetric synthesisen_US
dc.subject.lcshOrganic compounds--Synthesisen_US
dc.subject.lcshAmmonium compoundsen_US
dc.titleα,β-unsaturated acyl ammonium intermediates in asymmetric organocatalysisen_US
dc.typeThesisen_US
dc.contributor.sponsorEngineering and Physical Sciences Research Council (EPSRC)en_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US


The following license files are associated with this item:

  • Creative Commons

This item appears in the following Collection(s)

Show simple item record