Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.720304
Title: Lewis base-catalysed enantioselective formal cycloadditions and rearrangements
Author: Kasten, Kevin
Awarding Body: University of St Andrews
Current Institution: University of St Andrews
Date of Award: 2017
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Abstract:
This thesis describes the use of chiral nitrogen-based Lewis base catalysts in transformations such as cycloadditions and rearrangements. Cinchona alkaloids were employed as catalysts within a formal [4+2]-cycloaddition of trifluoromethyl- substituted α,β-unsaturated ketones and allenoates. Either 1,1,1-trifluorobut-3-en-2- ones or 4,4,4-trifluorobut-2-en-1-ones were used to selectively introduce a trifluoromethyl moiety in the 4- or 6-position within a dihydropyran scaffold. The reaction proceed successfully to give a range of dihydropyran products with (hetero)aryl- and alkyl-substituted trifluoromethyl ketones in up to 81% yield and 98% e.e. The dihydropyran products can be derivatised using selective hydrogenation methods to give tetrahydropyrans in high yield and diastereoselectivity without loss of stereointegrity. Furthermore, isothioureas were applied in the [2,3]-sigmatropic rearrangement of 3- fluorocinnamyl substituted quaternary ammonium salts. A broad range of substituents at either the nitrogen or the cinnamyl group has been evaluated showing the generality of this process. Enantioenriched amino acid derivatives containing a tertiary flourinated carbon centre were produced in high yield and good enantio- and diastereoselectivity (up to 76%, 94:6 d.r., 96% e.e.). It was attempted to extend the scope of this reaction to the [2,3]-Sommelet-Hauser rearrangement of benzylic ammonium salts, which proved to be difficult. A range of conditions as well as variety of substituted benzyl substrates were investigated but no rearrangement product could be isolated. The further extension of the scope of the [2,3]-rearrangement using allylic ammonium salts with 3-methylcinnamyl substitution was investigated. Mixtures of enantioenriched products derived from [2,3]- and [1,2]-rearrangement were observed. The fomation of the [1,2]-product led to the further investigation of this rearrangement. Applying ammonium salts bearing bulky 3,3-disubstituted allyl groups a selective [1,2]-rearrangement has been observed. The optimisation of this process is discussed and products were obtained in up to 68% yield and 58% e.e. This represents the first catalytic enantioselective [1,2]-rearrangement of ammonium salts.
Supervisor: Smith, Andrew D. Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.720304  DOI: Not available
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