Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373014
Title: Mechanistic and synthetic aspects of the photochemistry of spiro-oxaziridines
Author: Johnson, Graham P.
ISNI:       0000 0001 3591 1435
Awarding Body: Loughborough University of Technology
Current Institution: Loughborough University
Date of Award: 1986
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Abstract:
The photo-rearrangements of certain spiro-oxaziridines derived from tetral-1-one have been investigated in order to establish the effect of competition between aryl and alkyl migration and to examine the photochemistry of these systems when the N-substituent suffers steric compression. A range of spiro-oxaziridines having the N-substituent in the syn-aryl or anti-aryl configuration have been converted to the corresponding lactams, either as mixtures of regio-isomers or single substances. It has been demonstrated that stereo-electronically controlled photo-rearrangements (migration of the bond anti- to the lone-pair of electrons on the nitrogen atom) occur when the N-substituent is anti- to the aromatic ring. Reduced regio-specificity of the photo-rearrangement of syn-spiro-oxaziridines suggests that the first formed N–O bond cleaved species has a significant lifetime. The synthetic utility of the photo-rearrangement of the anti-aryl oxaziridine has been demonstrated by the preparation of a range of tricyclic, heterocyclic compounds, including pyrrolo-benzazepinones, pyrrolo-isoquinolinones and azeto-benzazepinones. The photo-products may have potential pharmacological activity.
Supervisor: Not available Sponsor: SERC
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.373014  DOI: Not available
Keywords: Organic chemistry
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