Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.761548
Title: An organoiron approach towards the enantioselective synthesis of hippeastrine
Author: Delf, Sarah
ISNI:       0000 0004 7652 5911
Awarding Body: University of East Anglia
Current Institution: University of East Anglia
Date of Award: 2017
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
This thesis describes work towards an organoiron approach towards the enantioselective synthesis of the alkaloid hippeastrine, starting from enantiomerically defined arene cis diols that can be made by biodioxygenation. Literature reviews of the target class of alkaloids, biodioxygenation, and the stereocontrolled applications of cationic electrophilic pentahapto cyclohexadienylium complexes, and the description of original work on biodioxygenation using R eutropha, and a series of new studies of complexation, activation, and nucleophile addition reactions using the organoiron approach are presented, supported by an Experimental Section to provide details of experimental procedures and compound characterisation.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.761548  DOI: Not available
Share: