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Towards designing de novo (1--->4)-linked polysaccharides

Carbohydrates are invaluable in a variety of industrial applications ranging from biodegradable materials to pharmaceutical drug carriers. Small functional groups, such as hydroxyl, amine, N-acetylamide and methoxy are commonly employed for creating de novo saccharides with enhanced functionality. T...

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Main Author: Chen, Jeff Yu-Jen
Format: Thesis
Language:English
Published: Department of Chemistry 2024
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access_status_str Open Access
author Chen, Jeff Yu-Jen
author_browse Chen, Jeff Yu-Jen
author_facet Chen, Jeff Yu-Jen
author_sort Chen, Jeff Yu-Jen
collection Thesis
description Carbohydrates are invaluable in a variety of industrial applications ranging from biodegradable materials to pharmaceutical drug carriers. Small functional groups, such as hydroxyl, amine, N-acetylamide and methoxy are commonly employed for creating de novo saccharides with enhanced functionality. The physiochemical properties of carbohydrates are governed by their conformations and the polarity of their substituents strongly influences the overall flexibility of such biomolecules. In this thesis, two types of (1--->4)-inter-glycosidic interactions, viz. hydrogen bonding and hydrophobic effects, are investigated.
format Thesis
id oai:open.uct.ac.za:11427/40104
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:33:54.099Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2024
publishDateRange 2024
publishDateSort 2024
publisher Department of Chemistry
publisherStr Department of Chemistry
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/40104 Towards designing de novo (1--->4)-linked polysaccharides Chen, Jeff Yu-Jen Chemistry Carbohydrates are invaluable in a variety of industrial applications ranging from biodegradable materials to pharmaceutical drug carriers. Small functional groups, such as hydroxyl, amine, N-acetylamide and methoxy are commonly employed for creating de novo saccharides with enhanced functionality. The physiochemical properties of carbohydrates are governed by their conformations and the polarity of their substituents strongly influences the overall flexibility of such biomolecules. In this thesis, two types of (1--->4)-inter-glycosidic interactions, viz. hydrogen bonding and hydrophobic effects, are investigated. 2024-07-02T09:27:18Z 2024-07-02T09:27:18Z 2004 2024-07-01T08:44:21Z Thesis / Dissertation Doctoral PhD http://hdl.handle.net/11427/40104 eng application/pdf Department of Chemistry Faculty of Science
spellingShingle Chemistry
Chen, Jeff Yu-Jen
Towards designing de novo (1--->4)-linked polysaccharides
thesis_degree_str Doctoral
title Towards designing de novo (1--->4)-linked polysaccharides
title_full Towards designing de novo (1--->4)-linked polysaccharides
title_fullStr Towards designing de novo (1--->4)-linked polysaccharides
title_full_unstemmed Towards designing de novo (1--->4)-linked polysaccharides
title_short Towards designing de novo (1--->4)-linked polysaccharides
title_sort towards designing de novo 1 4 linked polysaccharides
topic Chemistry
url http://hdl.handle.net/11427/40104
work_keys_str_mv AT chenjeffyujen towardsdesigningdenovo14linkedpolysaccharides