SINTESIS DUA ANALOG 4’-BROMO CALKON MELALUI KONDENSASI ALDOL DAN UJI ANTIOKSIDAN METODE FERI TIOSIANAT

dc.contributor.authorMaharani
dc.contributor.authorYuharmen
dc.contributor.authorEryanti, Y.
dc.date.accessioned2013-03-07T07:06:02Z
dc.date.available2013-03-07T07:06:02Z
dc.date.issued2013-03-07
dc.description.abstractChalcons are precursors of open chain flavonoids and isoflavonoids present in edible plants. Their derivatives have become attention for researchers because of their potentioal pharmacological effects. In finding of new efficient antioxidant compounds, substituted-chalcones have been synthesized by condensing benzaldehyde derivatives with 4’-bromoacetophenone in conventional method at room temperature based on Claisen-Schmidt condensation on alkali condition. The structures of the compounds were characterized by using infra red and nuclear magnetic resonance spectroscopy. In terms of antioxidant activity by using ferric thiocyanate (FTC) method, the compounds showed moderate antioxidant activityen_US
dc.description.sponsorshipYuharmen, Eryanti, Y.en_US
dc.identifier.otherRangga Dwijunanda Putra
dc.identifier.urihttp://repository.unri.ac.id:80/handle/123456789/2485
dc.language.isootheren_US
dc.subjectchalconeen_US
dc.subjectantioxidant activityen_US
dc.subjectferric thiocyanate methoden_US
dc.titleSINTESIS DUA ANALOG 4’-BROMO CALKON MELALUI KONDENSASI ALDOL DAN UJI ANTIOKSIDAN METODE FERI TIOSIANATen_US
dc.typeOtheren_US

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