The various groups into which the triterpenes are divided are defined and emphasis is placed on the structural relationships which exist between these groups. A brief description is given of the methods used in the determination of the structure of triterpenes with particular reference to β-asyrin (I), a member of the oleanane (II) group. Recent progress in the problems of biogenesis and the total synthesis of triterpenes is reviewed. All approaches, so far investigated, to the synthesis of pentacyclic triterpenes involve the fusion of two bicyclic moities representing rings A and B and rings D and E of the proposed structure. This thesis describes attempts to synthesise pentacyclic triterpenes of the oleanane (II) group, via the tetracyclic-cis-ketone (IIIa), the tetracyclic-trans-ketone (IIIc) or the tetracyclic-αβ-unsaturated-ketone (IVa).
| Identifer | oai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:459371 |
| Date | January 1972 |
| Creators | Hobbs, L. W. |
| Publisher | University of Oxford |
| Source Sets | Ethos UK |
| Detected Language | English |
| Type | Electronic Thesis or Dissertation |
| Source | http://ora.ox.ac.uk/objects/uuid:2ccf1035-ee1a-4c0b-a816-ad3d49c1d8f3 |
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