Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.657854
Title: Asymmetric synthesis of quaternary centres using organocatalysis
Author: Mitchell, A.
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 2009
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Abstract:
The task of creating an all carbon quaternary centre, bearing an alkyl moiety with differentiated functionalities and substituents is a desired key step in organic synthesis. A variety of endeavours by research groups have lead to the construction of stereogenic quaternary centres, albeit with narrow scope of substrate. Despite the repertoire of transition metals/ligand, chiral auxiliaries and reagents available at hand, efficient enantioselective and organocatalytic methodologies for the construction of all carbon quaternary centres still remains a daunting challenge for synthetic chemists. One of the most popular methods to install a quaternary centre is via a conjugate addition, the addition of a chiral tertiary enolate to an electron deficient alkene or carbonyl compound has led to high levels of synthetic accomplishment over generations. Our strategy to assemble such quaternary centres focused on an organocatalytic tandem. Michael-aldol reaction, as an efficient one-pot strategy to install vicinal quaternary centres with good levels of enantioselective induction. Initial 1, 4-conjugate addition of the nucleophile with a-acrolein type Michael acceptors generates the enolate, which is now set up to undergo an intramolecular aldol reaction providing the desired molecules. Molecular complexes of this class are also amenable to further catalytic transformations and synthetic elaborations. This thesis presents our investigations towards organocatalytic enantioselective strategies for the assembly of fully substituted quaternary centres.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.657854  DOI: Not available
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