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Analogues of Natural Product-like Scaffolds: Synthesis of Spiroacetal Derivatives

Diversity-oriented synthesis (DOS) involves the synthesis of several synthetic targets by transforming a collection of structurally simple and similar starting materials into a collection of structurally more complex and diverse products. This thesis describes the elaboration of a 6,6-spiroacetal scaffold to incorporate biologically useful moieties, in particular nucleobases, triazoles and amino acids, thus generating a collection of novel hybrid structures. The research reported, herein, focused on the synthesis of spiroacetal-nucleosides, triazoles and amino acids bearing a C8′-hydroxymethyl substituent.

Identiferoai:union.ndltd.org:AUCKLAND/oai:researchspace.auckland.ac.nz:2292/2628
Date January 2008
CreatorsChoi, Ka Wai
ContributorsProfessor Magaret Brimble
PublisherResearchSpace@Auckland
Source SetsUniversity of Auckland
LanguageEnglish
Detected LanguageEnglish
TypeThesis
RightsItems in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated., http://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm, Copyright: The author
RelationPhD Thesis - University of Auckland, UoA1829830

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