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Title: 14-hydroxycodeine and derivatives
Author: Currie, Andrew Cochran
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1961
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A series of 14-substituted codeine derivatives were prepared for pharmacological study by sodium borohydride reduction of the corresponding 14-hydroxy and 14-acyloxycodeinones. The epimeric 14-substituted isocodeines were not formed by this reaction but were prepared using 14-hydroxycodeine tosylate as an intermediate. The latter compound on treatment with 70% acetic acid gave the l4-hydroxyallopseudocodeine series. Lithium aluminium hydride reduction of 14-hydroxycodeine tosylate gave 14-hydroxydeoxycodeine and the very active analgesics, the 14-acyloxydeoxycodeines. Attempts to prepare known codeine derivatives from "hydroxy-codeine", the non-phenolic compound from the reaction of zinc dust and acetic acid on 14-hydroxycodeinone are described and a new structure is postulated. A new method is reported for the synthesis of 14-hydroxy-N-alkylnorcodeines. This involves the formation of 14-hydroxy-N-acylnorcodeine derivatives from the corresponding 14-acyloxy-N-cyano compound by acyl migration, and their reduction with lithium aluminium hydride.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available