Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728105
Title: Biocatalytic asymmetric synthesis of biaryl atropisomers
Author: Staniland, Samantha
ISNI:       0000 0004 6497 7777
Awarding Body: University of Manchester
Current Institution: University of Manchester
Date of Award: 2016
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Abstract:
Biaryl atropisomers are common structural motifs in natural products but most importantly they are used as chiral ligands in asymmetric catalysis. Despite their utility, current methods to synthesise them are limited and lack generality. Often ligands such as QUINAP have to be synthesised as the racemate and are resolved using stoichiometric palladium which is expensive and time consuming. Biocatalytic synthesis of biaryl atropisomers offers a new alternative greener route to their production. A biocatalytic redox desymmetrisation of symmetrical biaryl diols using a mutant of galactose oxidase (M3-5) is reported. Desymmetrised biaryl atropisomers were produced in good to excellent ee and yield for a range of substrates. After the desymmetrisation a partial kinetic resolution increased the ee further as the minor enantiomer was converted to the dialdehyde. The first example of biocatalytic dynamic kinetic resolution to synthesise atropisomers asymmetrically has been developed. Freely rotating biaryl N-oxide aldehydes underwent reduction using a ketoreductase enzyme to give biaryl N-oxide products in excellent ee (96-99%). These products were found to be novel Lewis base organocatalysts for the asymmetric allylation of benzaldehyde derivatives.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.728105  DOI: Not available
Keywords: Biocatalysis ; Atropisomers
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