Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.605611
Title: Enantioselective organocatalytic ammonium enolate mediated transformations and studies towards the total synthesis of (-)-galanthamine
Author: Johansson, C. C. C.
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2006
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Abstract:
(1) An enantioselective organocatalytic ammonium enolate mediated intramolecular cyclopropanation reaction has been developed. Studies towards an asymmetric intramolecular epoxidation reaction as well as an organocatalytic cycloisomerisation reaction have also been undertaken. These processes are catalysed by cinchona alkaloid derivatives, of which a novel class, bearing an alkyl substituent in the 2-position of the quinoline moiety, has been developed. The intramolecular cyclopropanation reaction provided bicycle[4.1.0]alkanes in good yields (> 80%) and excellent e.e.’s (> 93%). The unoptimised e.e. for the intramolecular epoxidation was 40%, and e.e’s up to 95% were observed in the cycloisomerisation reaction. (Fig. 566397A) (2) Two novel concepts; trans-annular ring closure and “zip-up” strategy have been applied towards a synthesis of (-)-galanthamine. The racemic syntheses of advanced intermediates 212 and 226 were accomplished in few steps from commercially available starting materials.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.605611  DOI: Not available
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