Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.351512
Title: Studies related to the synthesis of bifunctional ellipticines
Author: Smith, Andrew D.
ISNI:       0000 0001 3417 9297
Awarding Body: University of Bath
Current Institution: University of Bath
Date of Award: 1984
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Abstract:
The work described in this thesis is concerned with the preparation of "dimeric" derivatives of 6H-pyrido-5,11-dimethyl[4,3-b] carbazole (ellipticine) (1) . 9-Hydroxyellipticine (4) was prepared and esterified with adipic acid. 6-Hydroxy-l, 4-dimethylcarbazole was synthesised as a model compound, and the alkylation of this material was studied. A synthesis of 1-butylellipticine from 1,4-dimethylcarbazole was attempted, but resulted in the formation of a "dimeric" carbazole derivative. The synthesis of ellipticines bearing various substituents at position 3- was attempted starting from 1,4-dimethylcarbazoles. The final section describes attempts to prepare ellipticines with various 5-substituents starting from 3-[1-[3'-(4-cyanopyridyl)] ethyl] indole. Two 5-alkenyl-ellipticines were prepared by this route, and the reactivity of the alkenyl side chains was studied.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.351512  DOI: Not available
Keywords: Organic chemistry
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