Studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents
Includes bibliographical references (leaves 107-111). === The first part of the thesis describes synthesis of 10-( 4-methoxyphenyl)-4,5,9-trithia-deca- 1 ,6-diene (25) as an ajoene mimic and as a mixture of EIZ-geometrical isomers using new synthetic methodology. 4,5,9-trithia-dodeca-1,6-diene 9-oxi...
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Online Access: | http://hdl.handle.net/11427/9281 |
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ndltd-netd.ac.za-oai-union.ndltd.org-uct-oai-localhost-11427-92812021-06-25T05:08:50Z Studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents Qwebani, Tozama Hunter, Roger Caira, Mino R Chemistry Includes bibliographical references (leaves 107-111). The first part of the thesis describes synthesis of 10-( 4-methoxyphenyl)-4,5,9-trithia-deca- 1 ,6-diene (25) as an ajoene mimic and as a mixture of EIZ-geometrical isomers using new synthetic methodology. 4,5,9-trithia-dodeca-1,6-diene 9-oxide (43), 4,5,9-trithia-dodeca-,6- ene 9-oxide (44) and 2,3,7-trithia-deca-4-ene 7-oxide (45) were also successfully synthesized as a mixture of EIZ- separable geometrical isomers using the same synthetic methodology. The synthesis involved a radical addition and a chemoselective oxidation as key steps. Characterisation was carried out by [1]H NMR, [13]C NMR, IR and HRMS spectroscopies. 2014-11-05T17:41:59Z 2014-11-05T17:41:59Z 2009 Master Thesis Masters MSc http://hdl.handle.net/11427/9281 eng application/pdf University of Cape Town Faculty of Science Department of Chemistry |
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language |
English |
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Dissertation |
sources |
NDLTD |
topic |
Chemistry |
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Chemistry Qwebani, Tozama Studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents |
description |
Includes bibliographical references (leaves 107-111). === The first part of the thesis describes synthesis of 10-( 4-methoxyphenyl)-4,5,9-trithia-deca- 1 ,6-diene (25) as an ajoene mimic and as a mixture of EIZ-geometrical isomers using new synthetic methodology. 4,5,9-trithia-dodeca-1,6-diene 9-oxide (43), 4,5,9-trithia-dodeca-,6- ene 9-oxide (44) and 2,3,7-trithia-deca-4-ene 7-oxide (45) were also successfully synthesized as a mixture of EIZ- separable geometrical isomers using the same synthetic methodology. The synthesis involved a radical addition and a chemoselective oxidation as key steps. Characterisation was carried out by [1]H NMR, [13]C NMR, IR and HRMS spectroscopies. |
author2 |
Hunter, Roger |
author_facet |
Hunter, Roger Qwebani, Tozama |
author |
Qwebani, Tozama |
author_sort |
Qwebani, Tozama |
title |
Studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents |
title_short |
Studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents |
title_full |
Studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents |
title_fullStr |
Studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents |
title_full_unstemmed |
Studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents |
title_sort |
studies on the synthesis, cyclodextrin inclusion and biological activity of ajoene analogues as potentially novel anti-cancer agents |
publisher |
University of Cape Town |
publishDate |
2014 |
url |
http://hdl.handle.net/11427/9281 |
work_keys_str_mv |
AT qwebanitozama studiesonthesynthesiscyclodextrininclusionandbiologicalactivityofajoeneanaloguesaspotentiallynovelanticanceragents |
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1719412857862356992 |