Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.653751
Title: The synthesis of some α-diketones and a study of factors influencing the reactivity of the α-methylene group of unsymmetrical monoketones
Author: Leckie, Malcolm
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 1937
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Abstract:
A comparative study of the reactivity of the α-methylene groups of various types of ketones towards nitrous acid has been carried out and an attempt made to explain the results so obtained on a basis of the electronic arrangement of the compounds concerned. A number of α-diketones have been prepared by hydrolysis of the isonitroso- ketones (monoximes of diketones) by means of nitrous acid. One new diketone, acetyl valeryl was isolated and several derivatives were prepared. Diphenyl triketone was prepared in excellent yield by hydrolysis of isonitroso dibenzoyl methane with nitrous acid. An attempt to prepare ninhydrin by hydrolysis of the ß-oxime of 1:3 diketohydrindene with nitrous acid was unsuccessful the oxime being disrupted to give phthalic acid.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.653751  DOI: Not available
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