Asymmetric Diels-Alder Reactions of Acylnitroso Compounds

Snedden, Peter (1992) Asymmetric Diels-Alder Reactions of Acylnitroso Compounds. MSc(R) thesis, University of Glasgow.

Abstract

The Diels-Alder cycloaddition reactions of a small selection of transient C-nitroso compounds (two achiral and one chiral) were carried out with the unsymmetrically substituted, conjugated diene (E)-penta-1,3-diene 111 (piperylene). The aim of these experiments was to study the regiochemistry and any associated asymmetric induction of the cycloadducts. Acetohydroxamic acid 182d was oxidized, with periodate, in the presence of (E)-penta-1,3-diene 111 at 0

• Item Type: Thesis (MSc(R))
• Qualification Level: Masters
• Keywords: Organic chemistry
• Date of Award: 1992
• Depositing User: Enlighten Team
• Unique ID: glathesis:1992-78420
• Copyright: Copyright of this thesis is held by the author.
• Date Deposited: 28 Feb 2020 12:09
• Last Modified: 28 Feb 2020 12:09
• URI: https://theses.gla.ac.uk/id/eprint/78420