Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah
The main objective of this project is to synthesize a stilbene analogue, 4-acetoxy-l 1,13- dibenzyloxystilbene at large scale in order to supply for bioactivity and reactivity investigations by other researchers. Three established reactions have been used in order to accomplish the project. First, t...
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my.uitm.ir.986572024-07-22T08:02:14Z https://ir.uitm.edu.my/id/eprint/98657/ Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah Abu Samah, Nor Hayati RM Therapeutics. Pharmacology RS Pharmacy and materia medica The main objective of this project is to synthesize a stilbene analogue, 4-acetoxy-l 1,13- dibenzyloxystilbene at large scale in order to supply for bioactivity and reactivity investigations by other researchers. Three established reactions have been used in order to accomplish the project. First, the protection ofp-iodophenol using acetic anhydride to yield p-iodophenylacetale followed by the protection of 3,5-dihydroxybenzaldehyde with benzyl bromide that produced 3,5-dibenzyloxybenzaldehyde. Subsequently, the 3,5-dibenzyloxybenzaldehyde is utilized as a starting material of the Wittig reaction. Product of the Wittig reaction and /j-iodophenylaceate are then used to synthesize the stilbene analogue. The synthesized compounds are then, purified by chromatographic techniques and sent for 'H-NMR characterization. Concisely, even though the compound of desired has failed to be obtained, an almost structurally identical compound has been successfully synthesized in small amount. 2005 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/98657/1/98657.PDF Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah. (2005) Degree thesis, thesis, Universiti Teknologi MARA (Kampus Puncak Alam). |
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RM Therapeutics. Pharmacology RS Pharmacy and materia medica Abu Samah, Nor Hayati Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah |
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The main objective of this project is to synthesize a stilbene analogue, 4-acetoxy-l 1,13- dibenzyloxystilbene at large scale in order to supply for bioactivity and reactivity investigations by other researchers. Three established reactions have been used in order to accomplish the project. First, the protection ofp-iodophenol using acetic anhydride to yield p-iodophenylacetale followed by the protection of 3,5-dihydroxybenzaldehyde with benzyl bromide that produced 3,5-dibenzyloxybenzaldehyde. Subsequently, the 3,5-dibenzyloxybenzaldehyde is utilized as a starting material of the Wittig reaction. Product of the Wittig reaction and /j-iodophenylaceate are then used to synthesize the stilbene analogue. The synthesized compounds are then, purified by chromatographic techniques and sent for 'H-NMR characterization. Concisely, even though the compound of desired has failed to be obtained, an almost structurally identical compound has been successfully synthesized in small amount. |
format |
Thesis |
author |
Abu Samah, Nor Hayati |
author_facet |
Abu Samah, Nor Hayati |
author_sort |
Abu Samah, Nor Hayati |
title |
Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah |
title_short |
Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah |
title_full |
Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah |
title_fullStr |
Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah |
title_full_unstemmed |
Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah |
title_sort |
synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / nor hayati abu samah |
publishDate |
2005 |
url |
https://ir.uitm.edu.my/id/eprint/98657/1/98657.PDF https://ir.uitm.edu.my/id/eprint/98657/ |
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1806422116493426688 |
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13.211869 |