Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263637
Title: Stereoselective synthesis using aminyl radicals derived from α-amino acids
Author: Lewis, Kirk Alexander
ISNI:       0000 0001 3609 0202
Awarding Body: Loughborough University
Current Institution: Loughborough University
Date of Award: 1997
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Abstract:
Chapter 1 is the introduction to the thesis. It contains an overview of amino acids and aminyl radicals. The amino acids section includes material on their synthesis through traditional methods and asymmetric syntheses, as well as the use of radical reactions in their formation. The aminyl radical section gives a description of the nature of the radical and then proceeds with general techniques for aminyl radical formation. A more detailed account of our own group's use of sulfenamides and imines in aminyl radical formation is ·covered and the chapter is ended with a look at the work of aminyl radicals in amino acid synthesis and my subsequent intentions in this area. The preparation and cyclisation of sulfenamide precursors derived from [alpha]-amino acids is discussed in chapter 2. Both the cyclisations of aminyl and urethanyl (introduction of benzyloxycarbonyl and tosyl protecting groups onto amine) radicals onto suitably placed alkenyl substituents were investigated. 5-Exo-trig cyclisation reactions successfully afforded the cyclic products in moderate yield with reasonable diastereoselectivity. The effects of the [alpha]-CO2R (where R = Me or tBu), the size of the amino acid side chain and placement of alkenyl substituent (N-substituted or sidechain containing alkene) are discussed. The use of imines as aminyl radical precursors is explored in chapter 3. [Alpha]-amino acids and aldehydes were condensed and the cyclisation products isolated. The formation of aminyl radicals by 5-exo-trig cyclisation and subsequent H-atom abstraction gave moderate to good yields of N-cyclopentyl substituted a-amino acids. Preparation of the aldehydes is discussed. Tandem cyclisations involving aspects of chapters 2 and 3 are looked at in chapter 4. The preparation of the unnatural a-amino acids required for tandem cyclisation and subsequent formation of the sulfenamide or imine is reported. 5-Exo, 6-exo cyclisation of the sulfenamide derivative gave the tandem product in low yield and with moderate diastereoselectivity. This was in contrast to the imine derived reaction which proved unsuccessful. The remaining chapters incorporate the detailing of experimental relevant to the discussion and the presentation of references quoted throughout the thesis.
Supervisor: Not available Sponsor: Roche Holding AG
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.263637  DOI: Not available
Keywords: Sulfenamides; Imines
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