Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.787506
Title: Amino acid substituted guanidines as organocatalysts
Author: Al-Taie, Zahraa
ISNI:       0000 0004 7972 6196
Awarding Body: Bangor University
Current Institution: Bangor University
Date of Award: 2019
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Abstract:
A series of amino acid substituted guanidines of general structure I and II (AA = L-Proline, L-alanine and L-phenylalanine derivatives; (R, R1, R2 = H, Me, Alkyl, Aryl, Boc, Cbz) were prepared and their applications in asymmetric Michael reactions investigated. Initially, the project focused on the synthesis a range of N-alkylated-L-proline amides of several guandines. The catalysts prepared were applied to the Michael reaction between 2-nitrostyrene III and quinone IV leading to the conjugate product V in 17-99% yield and up to 56% enantiomeric excess. Hydrazine and several heterocyclic derivatives were also prepared which proved less effective. A series of N,N-dimethyl-L-alanine and N,N-dimethyl-L-phenylalanine derivatives were similarly prepared and these gave enantioselectivities of up to 31% ee in this reaction. The influence of racemisation of these catalysts during CDI coupling was also studied. Finally, N-protected-L-proline, L-alanine and L-phenylalanine derivatives were prepared to counter the observed racemisation and these gave enantioselectivities of up to 26% ee. X-ray crystallographic structures were determined for several of these compounds and the hydrogen bonding patterns observed were used to speculate on the mechanism of the reaction and the magnitude of the asymmetric induction observed. The X-ray crystallographic results proved that partial racemisation was occurring during the formation of the catalysts in a CDI mediated coupling reaction.
Supervisor: Murphy, Patrick Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.787506  DOI: Not available
Keywords: asymmetric orhganocatalysts
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