Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.795693
Title: Studies on macrocyclic acetylenic compounds
Author: McMaster, Denis
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1970
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
Section I In an attempt to synthesise compounds related to the as yet unknown 1,6-didehydro-[10]-annulene, intermolecular Castro type coupling of the cuprous salts of l-(o-iodophenyl)-2-propyn-1-ol and derivatives was investigated. Intermolecular coupling of derivatives suggested by model reactions was either unsuccessful, however, or gave a complex mixture, the nature of which could not be clarified. The synthesis of 'half-cyclised' compounds, formally only one stage away from the desired ten membered ring system was achieved, however, and some new examples of the Castro reaction, including some anomalies and failures, were discovered. Section II Intermoleeular Castro-type coupling of the cuprous salt of m-iodophenylacetylene was found to give a complex mixture, the major component of which was shown to be the 'cyclic pentamer' derived from five molecules of the cuprous salt. Evidence was obtained for the presence of similar cyclic compounds of lower and higher molecular weight. A series of compounds resulting from mixed oxidative and Castro-type coupling was also isolated from the reaction product.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.795693  DOI: Not available
Share: