Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692694
Title: Towards the development of asymmetric 6Pi electrocyclisations
Author: Parra, Guillaume
ISNI:       0000 0004 5919 556X
Awarding Body: University of Nottingham
Current Institution: University of Nottingham
Date of Award: 2014
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Restricted access.
Access from Institution:
Abstract:
The biosynthesis of the superfamily of pyrones such as (+)-tridachione, (-)-crispatone or tridachiahydropyrone have drawn much attention. However, the isolated natural products are enantiomerically pure whereas the syntheses of these natural products were completed in racemic form. This raises the question of where, in nature, the chirality is derived from. It has been hypothesized that the all (E)-polyene tridachiahydropyrone precursor is present in the membrane of the producing mollusc, and during the reaction the membrane provides a favourable chiral environment for obtaining only the tridachiahydropyrone enantiomer. The project aims to use different systems that mimic the cell membrane of the sacoglossan to show that a chiral environment induce chirality for electrocyclisations such as beta-cyclodextrin and chiral liquid crystals. Also, our efforts were towards the development of novel asymmetric 6Pi electrocyclic reactions that exploit catalyst-induced enantioselectivity with a secondary amine such as proline or (S)-alpha,alpha-diphenylprolinol, (S)-alpha,alpha-diphenylprolinol silylether, and MacMillan’s catalyst second generation. Unfortunately, all these electrocyclic reactions gave a racemic mixture.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.692694  DOI: Not available
Keywords: QD241 Organic chemistry
Share: