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首页> 外文期刊>ChemCatChem >Recent Progress in Metal Catalyzed Direct Carboxylation of Aryl Halides and Pseudo Halides Employing CO2 : Opportunities for C-11 Radiochemistry
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Recent Progress in Metal Catalyzed Direct Carboxylation of Aryl Halides and Pseudo Halides Employing CO2 : Opportunities for C-11 Radiochemistry

机译:芳基卤化物直接羧化的最近进展和伪卤化物采用CO 2:C-11放射化学的机会

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摘要

Carbon dioxide (CO2) as a synthon in organic transformations is very useful, especially when combined with transition metal catalysts. CO2 insertion on carbon(Aryl)-metal is are an elegant route to construct carbon-carbon bonds. A limited number of reports have been published to date on the direct conversion of aryl halides (or pseudo halides) to aryl carboxylic acids using transition metal catalysts. These reactions place great demand on the choice of catalyst, starting material, and reducing agent. However, these approaches could be of interest for the synthesis of a wide range of biologically active small molecules. Such transformations have already been applied for the synthesis of radiolabeled compounds for imaging with positron emission tomography (PET) using cyclotron produced [C-11]CO2 and may be applicable to the production of a diverse range of PET tracers.
机译:二氧化碳(CO 2)作为有机转化中的合成硅非常有用,特别是当与过渡金属催化剂结合时。 CO2碳(芳基)碳(芳基)是碳碳键的优雅途径。 使用过渡金属催化剂将迄今为止迄今为止迄今为止迄今为止芳基卤化物(或假卤化物)的直接转化为芳基羧酸。 这些反应对催化剂,起始材料和还原剂的选择提供了极大的需求。 然而,这些方法对于合成各种生物活性小分子的兴趣可能是有意义的。 已经应用这种转化用于合成使用回旋环(P-11] CO 2的带正电子发射断层扫描(PET)对放射性标记化合物的合成,并且可以适用于生产各种宠物示踪剂。

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