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Ferrous-catalyzed Artemisinin And Some Of The Reaction With Thiol Compounds

Posted on:2007-11-08Degree:MasterType:Thesis
Country:ChinaCandidate:F GaoFull Text:PDF
GTID:2191360185469675Subject:Organic Chemistry
Abstract/Summary:PDF Full Text Request
This paper reviewed the discovery and the further studies on qinghaosu over the last decades in the field of medicinal chemistry and some pharmacological researches, and summarized antimalarial mechanisms of artemisinin. Qinghaosu is originated from traditional herb-a widespread weed qinghao, Artemisia annua L. It is the most promising one of antimalarial compounds due to its outstanding antimalarial activity and lowest toxicity. We've explored the free radical cleavage of artemisinin by ferrous ion in the presence of homocysteine. A new compound called Y1 was obtained in this reaction, and its structure was characterized by means of its 1H NMR, 13C NMR, ESI-MS, elemental analysis data, and X-ray crystal structural analysis. The reasonable explanation was given.
Keywords/Search Tags:Artemisinin, homocysteine, cleavage, single crystal
PDF Full Text Request
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