Loughborough University
Leicestershire, UK
LE11 3TU
+44 (0)1509 263171
Loughborough University

Loughborough University Institutional Repository

Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/15431

Title: Some oxidation reactions utilizing hydrogen peroxide adducts in combination with carboxylic anhydrides
Authors: Newbold, Amanda J.
Issue Date: 1991
Publisher: © Amanda J. Newbold
Abstract: Interest grew in the development of new oxidising agents as a replacement for high purity meta-chloroperbenzoic acid (mCPBA) and avoiding the difficulty in obtaining high strength hydrogen peroxide. Magnesium monoperoxyphthalate (MMPP) has been advertised as a replacement. However due to problems of solubility of this oxidant in a number of solvents, it cannot be considered as a complete substitute for mCPBA. An oxidising agent is required to either complement MMPP, or succeed mCPBA entirely. This thesis describes the investigation of some hydrogen peroxide adducts as a possible contender to the extremely versatile oxidant, mCPBA. Urea-hydrogen peroxide adduct (UHP) in combination with either trifluoroacetic or acetic anhydride was used for the in situ formation of percarboxylic acids. Oxidations of various functional groups were carried out using these peracids. Reactions include: the epoxidation of terminal, electron deficient alkenes, such as octene, by trifluoroperacetic acid; the epoxidation of electron rich alkenes, such as styrenes and cyclohexenes, by peracetic acid; Baeyer-Villiger reactions of both aliphatic and alkyl aryl ketones by trifluoroperacetic acid; the conversion of anilines into nitrobenzenes; the oxidation of tertiary amines and sulphides; and the oxidative cleavage of dimethylhydrazones. A number of other hydrogen peroxide adducts were produced and their performance in various oxidation reactions was compared to that of ureahydrogen peroxide. Experiments in the formation of adducts to induce chirality in epoxidation reactions were also undertaken.
Description: A Doctoral Thesis. Submitted in partial fulfilment of the requirements for the award of Doctor of Philosophy of Loughborough University.
URI: https://dspace.lboro.ac.uk/2134/15431
Appears in Collections:PhD Theses (Chemistry)

Files associated with this item:

File Description SizeFormat
Thesis-1991-Newboold.pdf3.11 MBAdobe PDFView/Open
Form-1991-Newbold.pdf45.76 kBAdobe PDFView/Open

 

SFX Query

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.