Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644807
Title: Studies towards the synthesis of the palmerolides
Author: Eadie, Scott
ISNI:       0000 0004 5358 1566
Awarding Body: University of St Andrews
Current Institution: University of St Andrews
Date of Award: 2014
Availability of Full Text:
Access through EThOS:
Access through Institution:
Abstract:
In 2006, Baker reported the isolation of palmerolide A, a polyketide derived marine macrolide, from the Antarctic tunicate Synoicum adareanum collected in the shallow waters surrounding Anvers Island. This unique macrolide displayed potent levels of cytotoxic activity in the human melanoma cell lines (UACC-62, LC₅₀ = 18 nM and M14 LC₅₀ = 76 nM), while also inhibiting V ATPase with an IC₅₀ of 2 nM. There have been eight further palmerolides isolated from Synoicum adareanum, which have been shown to possess cytotoxicity activity. The synthetic route devised for palmerolide A, utilised a convergent approach relying on the initial synthesis of three subunits. These subunits were to be coupled via a Horner-Wadsworth Emmons reaction, a Julia-Kocienski olefination, then followed by formation of the macrolcycle. This approach offers both flexibility and convergence, as alterations to the subunits would give access to other members of the palmerolide family and their analogues such as palmerolide E.
Supervisor: Florence, Gordon John Sponsor: Engineering and Physical Sciences Research Council (EPSRC) ; Cancer Research UK
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.644807  DOI: Not available
Keywords: Synthesis ; Natural product
Share: