Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.653825
Title: Cycloaddition reactions of jojoba oil
Author: Leslie, Morag Garden
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 1990
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Abstract:
The cycloaddition reactions of nitrile oxides with jojoba oil have been investigated. The nitrile oxides were generated in situ by two principal routes: (i) by the base catalysed dehydration of nitromethyl compounds using tolylene-2,4-diisocyanate (the Mukaiyama method), and (ii) by thermolysis of nitro-acetate and -malonate esters (the Shimizu method). In order to faciliate the identification of modified jojoba products and establish optimum conditions for reaction with the unsaturation present in jojoba oil, the cycloaddition reactions of nitrile oxides with selected model alkenes were studied. Terminal alkenes afforded 5-substituted-2-isoxazolines regiospecifically in 21-68% yield, whereas mid-chain alkenes proved to be less reactive and gave a regioisomeric mixture of 4,5- disubstituted isoxazolines (19-69&37 yield). Cycloadditions to unsaturated lipids were also examined; methyl oleate and oleyl acetate both yielded stereospecifically a regioisomeric mixture of cis- isoxazolines when reacted with ethoxycarbonylnitrile oxide. The geometric isomer of methy oleate, methyl elaidate, afforded a mixture of trans-4,5-disubstituted isoxazolines. The ratio of regioisomers in all cases was shown to be 1:1 by the use of high field 13C NMR, which detected small differences in chemical shifts of ring carbons. Proton NMR was also used to characterise lipid isoxazolines, assignment of their spectra being facilitated by comparison with those of model compounds. FAB mass spectrometry enabled the detection of parent ions for these isoxazolines. Application of the Shimizu method to ethyl nitroacetate provided a novel approach to formonitrile oxide; with model alkenes 3-unsubstituted isoxazolines were formed in 19-36% yields. In contrast, ethyl nitroacetate reacted with isocyanate and base to form N-phenyl-α-ethoxycarbonyl-α-nitroacetamide which was itself thermolysed to produce an amide nitrile oxide. Further exploitation of this approach using di-isocyanates lead to the generation of di-nitrile oxides. Cycloaddition reactions of the analogous azomethine oxide, C,N-diphenylnitrone, led to formation of the corresponding ring-saturated isoxazolidine moieties.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.653825  DOI: Not available
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