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Department of Chemistry

Cycloaddition studies in steroidal 14,16-dienes

Abstract

dc:description.abstract

Studies have been conducted in synthesising ring D-substituted steroidal 14,16-dienes. The aim was to explore the scope for carrying out cycloaddition reactions, and exploiting the built-in bridge substituents of derived 14,17-cycloadducts, for eventual conversion into bridge-functionalised 19-norsteroids.

Degree

thesis:*
Grantor dc:publisher.institution
Department of Chemistry
Year dc:date.issued
1991

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Loedolff, Michiel C
Advisor dc:contributor.advisor
  • Bull, James R

Rights

Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/11427/17037
OAI identifier oai:identifier
oai:open.uct.ac.za:11427/17037

Chain of custody

source
Harvested from
University of Cape Town
Base URL
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Last updated
2026-07-22
Source record
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citation

Loedolff, Michiel C. Cycloaddition studies in steroidal 14,16-dienes. Department of Chemistry, 1991. http://hdl.handle.net/11427/17037