Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581268
Title: Studies towards the total synthesis of manzamine A
Author: Hawkins, Alison
Awarding Body: University of Oxford
Current Institution: University of Oxford
Date of Award: 2013
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Abstract:
This thesis describes studies towards the total synthesis of manzamine A (9), a marine alkaloid. Two routes are presented. The first route applied a novel palladium-catalysed arylative allene spirocyclisation cascade to the synthesis of manzamine A (9). In the first generation, a short route was developed to access the tricyclic ACE core 263a in only nine steps. The second generation applied the palladium-catalysed cascade to a similar system which utilised non-terminal allene pro-nucleophile 450 in an attempt to access a homologated derivative of the ACE core. The second route relied on a diastereoselective Michael addition between nitro-olefin 473 and 8,5-fused ring system 146 comprising rings C and E of manzamine A (9). Further elaboration of the Michael addition product enabled the synthesis of tetracyclic ABCE core precursor 464 to be carried out and preliminary investigations into ring B formation were investigated.
Supervisor: Dixon, Darren Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.581268  DOI: Not available
Keywords: Organic synthesis ; Organic chemistry ; Natural products ; Chemistry & allied sciences ; Synthetic organic chemistry
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