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Title: Synthetic approaches to the cladiellin diterpenes
Author: Hewitt, Natalie L.
ISNI:       0000 0004 5351 4734
Awarding Body: Cardiff University
Current Institution: Cardiff University
Date of Award: 2015
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This thesis describes the result of synthetic efforts to apply a novel desymmetrisation process to the cladiellin diterpenes, an important group of natural products. The aim is to use the novel Prins-Wagner-Meerwein desymmetrisation of cyclohexa-1,4-dienes to prepare octahydroisobenzofuran structures that are closely related to the cladiellin diterpenes. Chapter 1 presents a short review of the 2,11-cyclised cembranoids including the cladiellin diterpene structures and previous synthetic efforts, followed by a brief discussion of the Prins cyclisation. This is followed by a description of previous work carried out within the Elliott group on the Prins desymmetrisation of cyclohexa-1,4-dienes that sets the stage for the work described in chapters 2 – 5. Chapter 2 describes the alkylation of cyclohexa-1,4-dienes using n-BuLi and TMEDA to give a direct and highly diastereoselective route to the corresponding 4-substituted products in which the alkyl group introduced is trans to the carboxylic acid. Chapter 3 describes the attempted application of Prins cyclisation/rearrangement methodology to the core of the cladiellin diterpenes. This was successful for a model compound containing a 6-membered ring, but when applied to compounds containing 7- and 9-membered rings, macrocyclic dimeric products were obtained. Chapter 4 describes an alternative synthetic strategy from that attempted in Chapter 3, to construct the cladiellin diterpene framework using a 6,5-fused system and cleaving of this to give a 9-membered ring system. Chapter 5 describes the successful synthesis of a model compound containing a fused aromatic ring using the strategy developed in Chapter 4.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: QD Chemistry