Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753966
Title: Intramolecular nitrene insertions into aromatic systems
Author: Carde, Robert N.
Awarding Body: Keele University
Current Institution: Keele University
Date of Award: 1974
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
A study of the intramolecular insertion reactions of aryl nitrenes is described. In Part I the preparation and photolytic decomposition of a number of aryl azides in diethylamine is described. The usual products were 3H-azepines but in one case ring expansion did not occur and the major product was an aryl amine. Attempts to prepare aza-azulenes and azepinium salts from certain of the decomposition products were unsuccessful. In Part II an account of the experiments used to determine the effect of annelation upon the nitrene insertion reaction is given. The decomposition of 1- and 2-(azidobenzyl)naphthalene was shown to give predominantly acridan and acridine products, while the tetrahydro derivatives, 5- and 6-(2-azidobenzyl) tetralin, gave the ring insertion products, benzazepinoindoles. The reasons for the differing reaction pathways are discussed. In Part III the preparation and thermal decomposition of a number of 2-azidotriphenylmethanes is described. The usual products were aoridans and azepinoindoles but in one case, when a 4'-methoxyl group was present in the azide, the major product was an 8,9-methanopyridoindole. Experiments to determine the nature of the [1,,3] hydrogen shift observed in the formation of the azepinoindoles are described. A mechanism is proposed which satisfactorily accounts for the observed products and product ratios.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.753966  DOI: Not available
Keywords: QD Chemistry
Share: