分子內Diels-Alder反應應用於天然物GuanacastepeneA之七、六駢環合成研究

碩士 === 國立清華大學 === 化學系 === 95 === Guanacastepene’s activity against methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecalis makes it of interest as a potential lead compound in the development of new antibacterial agents. We prepare trienyl compounds by combining...

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Bibliographic Details
Main Author: 鄭家任
Other Authors: 沙晉康
Format: Others
Language:zh-TW
Published: 2006
Online Access:http://ndltd.ncl.edu.tw/handle/41719290853811294487
Description
Summary:碩士 === 國立清華大學 === 化學系 === 95 === Guanacastepene’s activity against methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecalis makes it of interest as a potential lead compound in the development of new antibacterial agents. We prepare trienyl compounds by combining side chain of the diene with 3-methylcyclohept-2-enol. We form the cyclohexane ring by an intramolecular Diels-Alder reaction, which has been used to form related [5, 4, 0]undecane. Now, we have the part of the carbon skeleton of Guanacastepene A. Finally, we study the influence of methyl group of dienophile on intramolecular Diels-Alder reaction