G'/> <![CDATA[Synthesis of chiral carbosilane dendrimers with <ce:small-caps>l</ce:small-caps>-cysteine and <ce:italic>N</ce:italic>-acetyl- <ce:small-caps>l</ce:small-caps>-cysteine on their surface and their application as chiral selectors for enantiomer separation by capillary electrophoresis]]>
首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >l-cysteine and N-acetyl- l-cysteine on their surface and their application as chiral selectors for enantiomer separation by capillary electrophoresis]]>
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l-cysteine and N-acetyl- l-cysteine on their surface and their application as chiral selectors for enantiomer separation by capillary electrophoresis]]>

机译:<![cdata [CDATA [合成手性碳硅烷树枝状大分子的 l -cysteine和 n - 乙酰 - L - 毛细管的应用及其作为毛细管电泳对映体分离的手性选择器的应用]]]>

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Graphical abstractDisplay OmittedAbstractThe synthesis of chiral carbosilane dendrimers functionalized with cysteine andN-acetylcysteine groups is presented. These dendrimers were obtained through thiol–ene addition reactions and their application as chiral selectors in capillary electrophoresis was investigated. Four drugs used as model compounds were analyzed under different experimental conditions observing that the use of a first generation dendrimer containing 4 terminalN-acetyl-l-cysteine groups enabled the enantiomeric discrimination of razoxane with a discrimination power similar to that obtained with other powerful chiral selectors such as cyclodextrins.]]>
机译:<![cdata [ 图形摘要 显示省略 抽象 呈现用半胱氨酸和 n - 乙酰琥珀酸官能团官能化的手性碳硅烷树枝状大分子的合成。通过硫醇-NEE加入反应获得这些树枝状过处,并研究了它们的应用作为毛细管电泳中的手性选择器。在不同的实验条件下分析了用作模型化合物的四种药物,观察使用含有4个末端的第一代树枝状聚合物 n - 乙酰 - l -Cysteine基团使罗氧烷的对映体辨别具有类似于与其他强大的手性选择器(如环糊精)获得的歧视力。 ]]>

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