Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.461771
Title: Synthetic approaches to medium and large rings
Author: Kennedy, William Brian
ISNI:       0000 0001 3597 2975
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1974
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Abstract:
Synthetic routes to macrocyclic ketones and lactones via fused bicyclic, doubly bridged tricyclic and bridged tricyclic precursors have been investigated as follows : (a) The condensation of diethylsuccinylsuccinate and acrolein gave two interesting compounds. The first compound was identified as a fused tricyclic system, an oetahydroindacene-dione-dicarboxylic ester, whose structure was investigated and the ester groups found to be trans. The second was a complex bridged tetracyclic system, whose structure was elucidated by chemical and physical methods, including 13-C nmr spectroscopy, (b) The synthesis of cycloalkynones was investigated from Delta2,6-tricyclo-[6,3,1,0 2,6]-dodecan-5,12-diones by cleavage of the one-carbon bridge, followed by cleavage of the double bond by Eschenmoser's tosylhydrazone-epoxide ring opening reaction. The first half of this sequence was shown to be feasible, but lack of time precluded further investigation. A direct approach to macrocyclic lactones from Delta9-tetrahydrochroman-4-ones was not successful.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.461771  DOI: Not available
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