Towards designing de novo (1--->4)-linked polysaccharides
| dc.contributor.author | Chen, Jeff Yu-Jen | |
| dc.date.accessioned | 2024-07-02T09:27:18Z | |
| dc.date.available | 2024-07-02T09:27:18Z | |
| dc.date.issued | 2004 | |
| dc.date.updated | 2024-07-01T08:44:21Z | |
| dc.description.abstract | 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. | |
| dc.identifier.apacitation | Chen, J. Y. (2004). <i>Towards designing de novo (1--->4)-linked polysaccharides</i>. (). ,Faculty of Science ,Department of Chemistry. Retrieved from http://hdl.handle.net/11427/40104 | en_ZA |
| dc.identifier.chicagocitation | Chen, Jeff Yu-Jen. <i>"Towards designing de novo (1--->4)-linked polysaccharides."</i> ., ,Faculty of Science ,Department of Chemistry, 2004. http://hdl.handle.net/11427/40104 | en_ZA |
| dc.identifier.citation | Chen, J.Y. 2004. Towards designing de novo (1--->4)-linked polysaccharides. . ,Faculty of Science ,Department of Chemistry. http://hdl.handle.net/11427/40104 | en_ZA |
| dc.identifier.ris | TY - Thesis / Dissertation AU - Chen, Jeff Yu-Jen AB - 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. DA - 2004 DB - OpenUCT DP - University of Cape Town KW - Chemistry LK - https://open.uct.ac.za PY - 2004 T1 - Towards designing de novo (1--->4)-linked polysaccharides TI - Towards designing de novo (1--->4)-linked polysaccharides UR - http://hdl.handle.net/11427/40104 ER - | en_ZA |
| dc.identifier.uri | http://hdl.handle.net/11427/40104 | |
| dc.identifier.vancouvercitation | Chen JY. Towards designing de novo (1--->4)-linked polysaccharides. []. ,Faculty of Science ,Department of Chemistry, 2004 [cited yyyy month dd]. Available from: http://hdl.handle.net/11427/40104 | en_ZA |
| dc.language.rfc3066 | eng | |
| dc.publisher.department | Department of Chemistry | |
| dc.publisher.faculty | Faculty of Science | |
| dc.subject | Chemistry | |
| dc.title | Towards designing de novo (1--->4)-linked polysaccharides | |
| dc.type | Thesis / Dissertation | |
| dc.type.qualificationlevel | Doctoral | |
| dc.type.qualificationlevel | PhD |