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Department of Chemistry

Rhizophoraceae alkaloids : preliminary studies in the synthesis of Gerrardine

Abstract

dc:description.abstract

The synthesis envisaged the building of the dithiolane ring on to homoproline, the synthesis of which was effected from tetrahydrofurfuryl alcohol and from proline itself. The reactions involved in these syntheses are discussed with particular reference to the protection of the secondary nitrogen, the difficulties encountered in the application of the Arndt-Eistert reaction, and the possible application of the Prins reaction.

Degree

thesis:*
Grantor dc:publisher.institution
Department of Chemistry
Year dc:date.issued
1968

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Kleynhans, C R
Advisor dc:contributor.advisor
  • Warren, F L

Rights

Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/11427/13870
OAI identifier oai:identifier
oai:open.uct.ac.za:11427/13870

Chain of custody

source
Harvested from
University of Cape Town
Base URL
open.uct.ac.za/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
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citation

Kleynhans, C R. Rhizophoraceae alkaloids : preliminary studies in the synthesis of Gerrardine. Department of Chemistry, 1968. http://hdl.handle.net/11427/13870