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Title: Reactions and rearrangements of chroman-4-ones and related compounds
Author: Gabbutt, Christopher David
ISNI:       0000 0001 3486 0787
Awarding Body: Lancashire Polytechnic
Current Institution: University of Central Lancashire
Date of Award: 1987
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The synthesis of a range of novel 2,2-disubstituted chroman-4-ones has been accomplished by the pyrrolidine catalysed condensation of a 2-hydroxyacetophenone with aldehydes and ketones. The reaction permits access to both symmetrically and unsymmetrically substituted compounds. The reaction has been extended to the preparation of a novel furochromanone, an analogue of the natural product khellin. The Schmidt reaction of 2,2-disubstituted chroman-4-ones in an acetic-sulphuric acid mixture affords 2,3,4.5-tetrahydro-1.4- benzoxazepine-5(411)--ones, resulting from alkyl migration of the iminodiszonium intermediate. Chroman-4-ones possessing a carbocation stabilising function show anomalous behaviour, the initially formed 1,4-benzoxazepinone being particularly susceptible to protolysis. 2-Methyl-2-phenylchromanone affords a 2-oxazoline as the major product, whilst 2-cyclopropyl-2- methylchromanone gives a mixture of five components which have been separated and characterised. The major products result from hydration and acetolysis of the cyclopropyl carbenium ion. Products resulting from aryl migration and anti-Markovnikov addition of acetic acid to the cyclopropane ring are also formed. Carbanions derived from chromanones have been generated and used to prepare a range of 3-hydroxymethylenechroman-4-ones. Conjugate reduction of the corresponding chromone by sodium borohydride in pyridine provides a simple entry to 3-acetyl and 3-aroyl-2-methylchromanones. These dicarbonyl compounds are versatile intermediates and have been used to prepare a range of benzopyrano isoxazoles, pyrazoles. pyrroles and pyrimidines. 3-Hydroxymethylenespiro[chroman-2. 1 '-cyclopentan]-4-one is particularly unstable to acid-base conditions. Attempts to prepare this compound resulted only in the formation of 3-(1 cyclopentenyl)chromone, arising from a bond-switch operation initiated by fragmentation of the pyranone ring in a retro-Michael reaction. Conditions suitable for extension of this reaction to other 3-hydroxymethylenechromanones have been developed, affording access to a range of hitherto inaccessible 3-alkenylchromones. The regio- and stereo-chemical outcome of the reaction has been elucidated. Some preliminary investigations of the behaviour of 3-alkenyl chromones in Diels-Alder reactions are described.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: Chemistry