Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.795660
Title: Studies in the diterpenoid field
Author: Balmain, Allan
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1969
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Abstract:
The constitution and stereochemistry of epsilon-caesalpin, a furanoid diterpenoid from Caesalpinia bonducella, has been derived from chemical and spectroscopic evidence. The proposed structure was verified by x-ray analysis of a p-bromobenzoate derivative, which in addition provided the absolute configuration. An attempt to determine the absolute configuration of alpha-, beta- and delta-caesalpins by direct correlation with epsilon-caesalpin was unsuccessful. This research revealed several inconsistencies in the results of previous workers on the stereochemistry of these compounds, and evidence is presented which defines unambiguously the stereochemistry of the ring B substituents of alpha- (and hence beta- and delta-) caesalpin. The structures of six of the minor constituents of Caesalpinia bonducella are discussed. Extraction of the whole plant Andrographis paniculata afforded, in addition the known compounds andrographolide and neoandrographolide, three diterpenoid lactones which had not been previously isolated. The structures of these have been deduced from chemical and spectral data. The mass spectra of some andrographolide derivatives are discussed.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.795660  DOI: Not available
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