Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329386
Title: Synthetic approaches towards chiral leukotriene analogues
Author: Rogers-Evans, Mark C.
Awarding Body: Loughborough University of Technology
Current Institution: Loughborough University
Date of Award: 1989
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Abstract:
A review of the discovery, biological activity and chemical synthesis of the leukotrienes is presented, together with the latest developments in their structural modification to produce useful antagonists. Strategies are presented for the preparation of chiral leukotriene derivatives in which the characteristic triene unit is replaced by various aromatic groups and include: (i) The preparation and attempted separation of the racemic diastereomers of methyl S-hydroxy-6-(2-methoxycarbonyl- 2-amino-ethylthio > -6-phenylhexanoate; (ii) A chemical synthesis involving the Sharpless asymmetricepoxidation of (El-ethyl 4-hydroxy-6-phenylhex-S-enoate to (El-ethyl S( R).6(S)-epoxy-6-phenyl-4(S)-hydroxyhexanoate followed by selective de-oxygenation studies on the corresponding racemic epoxy alcohol to give (E}-ethyIS.6-epoxy-6-phenyl-hexanoate; iii An enzymic route utilizing the porcine pancreatic lipase catalysed hydrolysis of a number of racemic 3-alkyl-3-butanoyloxy- 1.2-epoxides to the corresponding chiral epoxy alcohols with various degrees of selectivity. one of the most useful being the completely enantioselective hydrolysis of the less polar diastereomer of· (E)-3-butanoyloxy-I.2-epoxy-I-phenylhexane. The more polar diastereomer was preferentially hydrolysed to l( R),2(S)-epoxy-I-phenylhexan-3-( R)-ol, as verified by Sharpless epoxidation of (E)-I-phenylhex-I-en-3-01.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.329386  DOI: Not available
Keywords: Leukotriene synthesis
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