Synthesis of hydroxylated and prenylated chalcones

Prenylated chalcones are among the compounds found in local Artocarpus species which reported to have interesting biological activities. Moreover, prenylated chalcones are used as traditional folk medicine for the treatment of inflammation, malarial fever and to treat the ulcers and diarrhea. In thi...

Full description

Saved in:
Bibliographic Details
Main Author: Hasan, Aso Hameed
Format: Thesis
Language:English
Published: 2013
Subjects:
Online Access:http://eprints.utm.my/id/eprint/39737/5/AsoHameedHasanMFS2013.pdf
Tags: Add Tag
No Tags, Be the first to tag this record!
id my-utm-ep.39737
record_format uketd_dc
spelling my-utm-ep.397372017-07-13T06:48:04Z Synthesis of hydroxylated and prenylated chalcones 2013-06 Hasan, Aso Hameed Q Science (General) Prenylated chalcones are among the compounds found in local Artocarpus species which reported to have interesting biological activities. Moreover, prenylated chalcones are used as traditional folk medicine for the treatment of inflammation, malarial fever and to treat the ulcers and diarrhea. In this study, 2,4-dihydroxy-3-C-prenylacetophenone and 2,4-dihydroxy-5-C-prenylacetophenone were successfully synthesized by treating resacetophenone with 2-methylbut-3-en-2-ol in the presence of BF3.Et2O as the catalyst. Meanwhile 2,4,6-trihydroxy-3-C-prenylacetophenone was synthesized using K2CO3 as the catalyst in dry acetone in the reaction of prenyl bromide with 2,4,6-trihydroxyacetophenone . In addition, two hydroxylated chalcone namely 2',4',4-trihydroxychalcone , 4',4-dihydroxychalcone) together with 2',4',4,6'-tetrahydroxy-3'-prenylchalcone were synthesized by Claisen-Schmidt condensation of various hydroxyacetophenone and 2,4,6-trihydroxy-3-C-prenylacetophenone for prenylated chalcone with 4-hydroxybenzaldyhe using BF3.Et2O. The structures of all compounds were characterized using spectroscopic methods (NMR and IR). 2013-06 Thesis http://eprints.utm.my/id/eprint/39737/ http://eprints.utm.my/id/eprint/39737/5/AsoHameedHasanMFS2013.pdf application/pdf en public masters Universiti Teknologi Malaysia, Faculty of Science Faculty of Science
institution Universiti Teknologi Malaysia
collection UTM Institutional Repository
language English
topic Q Science (General)
spellingShingle Q Science (General)
Hasan, Aso Hameed
Synthesis of hydroxylated and prenylated chalcones
description Prenylated chalcones are among the compounds found in local Artocarpus species which reported to have interesting biological activities. Moreover, prenylated chalcones are used as traditional folk medicine for the treatment of inflammation, malarial fever and to treat the ulcers and diarrhea. In this study, 2,4-dihydroxy-3-C-prenylacetophenone and 2,4-dihydroxy-5-C-prenylacetophenone were successfully synthesized by treating resacetophenone with 2-methylbut-3-en-2-ol in the presence of BF3.Et2O as the catalyst. Meanwhile 2,4,6-trihydroxy-3-C-prenylacetophenone was synthesized using K2CO3 as the catalyst in dry acetone in the reaction of prenyl bromide with 2,4,6-trihydroxyacetophenone . In addition, two hydroxylated chalcone namely 2',4',4-trihydroxychalcone , 4',4-dihydroxychalcone) together with 2',4',4,6'-tetrahydroxy-3'-prenylchalcone were synthesized by Claisen-Schmidt condensation of various hydroxyacetophenone and 2,4,6-trihydroxy-3-C-prenylacetophenone for prenylated chalcone with 4-hydroxybenzaldyhe using BF3.Et2O. The structures of all compounds were characterized using spectroscopic methods (NMR and IR).
format Thesis
qualification_level Master's degree
author Hasan, Aso Hameed
author_facet Hasan, Aso Hameed
author_sort Hasan, Aso Hameed
title Synthesis of hydroxylated and prenylated chalcones
title_short Synthesis of hydroxylated and prenylated chalcones
title_full Synthesis of hydroxylated and prenylated chalcones
title_fullStr Synthesis of hydroxylated and prenylated chalcones
title_full_unstemmed Synthesis of hydroxylated and prenylated chalcones
title_sort synthesis of hydroxylated and prenylated chalcones
granting_institution Universiti Teknologi Malaysia, Faculty of Science
granting_department Faculty of Science
publishDate 2013
url http://eprints.utm.my/id/eprint/39737/5/AsoHameedHasanMFS2013.pdf
_version_ 1747816544395591680