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Tandem reactions of oxiranylcarbinyl radicals

The work described in this thesis is an investigation into the reactivity and possible synthetic applications of oxiranylcarbinyl radicals. These radicals rapidly rearrange via β-cleavage, which can proceed by breakage of either the C-O or the C-C bond. Cleavage of the latter only occurs when the molecule has a vinyl or phenyl stabilising group attached to the epoxide ring.

Identiferoai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:362663
Date January 1997
CreatorsRudderham, John Andrew
PublisherLoughborough University
Source SetsEthos UK
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation
Sourcehttps://dspace.lboro.ac.uk/2134/27150

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