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ETUDE DU COMPORTEMENT ELECTROCHIMIQUE DE COMPOSES POLYFONCTIONNELS ET DE DERIVES COMPORTANT UN GROUPEMENT XANTHATE

机译:含黄酸酯基团的多功能化合物和衍生物的电化学行为研究

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摘要

Electrosynthesis is presented in a detailed manner with an emphasis on reactive electro-generated species and on their interactions (and those of the substrate) with the medium constituents (solvent, ions of electrolyte, constituents of the electrodes). These can act upon the regioselectivity when polyfonctionnal compounds are being processed. This approach has been applied (a) to natural products bearing different carbonyl groups (Chap.3) and (b) to xanthate derivatives (Chap.4 to 8). - On the first substrates (a), it was confirmed that the cation of the electrolyte exerts a preponderant effect upon the regioselectivity of the cathodic reductions. However, it has not been possible to pinpoint the respective role of the solvent or the cation. It is also possible that the anion has an effect on the reactivity of the cation. At the same time, we have conceived and tested a range of reactors of different sizes (from 1 to 50 cm3), with separate compartments, suited for use with solid electrodes (Chap.2). - With the second substrates (b), we present our electrochemical approaches for tree types of reactions: the introduction of the xanthate group, its elimination and the initiation of radical additions (Chap.4 to 8). - Attempts at the synthesis of xanthates by electrogeneration of tertiary radicals in presence of a bis-xanthate have failed. The latter was too easily reduced or oxidised under the Kolbe conditions (Chap.5). - The cathodic reduction of xanthates gave good yields but only with the derivatives of acetophenones. The anodic oxidation did not lead to cyclisation into tetralones (Chap.6). - The initiation of radical additions onto olefins by group transfer failed when using cathodic reduction of alkyl iodides. However, we observed a new reaction when operating with cathodes possessing a strong electro-catalytic activity (Ag, Au, Pd). It consists in the addition of the radical from ethyl iodo-acetate onto a primary xanthate, followed by a cyclisation (Chap.7). In addition, we conceived and tested systems with electric relays for inverting the polarity of the electrodes in order to clean their surfaces when adsorption inhibited the flow of current. - The initiation reactions gave promising results in the case of anodic oxidation of partially neutralised malonic acid. But the yields must be improved further (yield : 45 %; corrected intermediate yield : 75 %) (Chap.8).
机译:详细介绍了电合成,重点是反应性电生成物质及其与介质成分(溶剂,电解质离子,电极成分)的相互作用(以及基体的相互作用)。当加工多官能化合物时,这些可以作用于区域选择性。该方法已应用于(a)带有不同羰基的天然产物(第3章),(b)应用于黄药衍生物(第4至8章)。 ·在第一基材(a)上,证实了电解质的阳离子对阴极还原的区域选择性发挥了主要作用。但是,不可能精确指出溶剂或阳离子的各自作用。阴离子也可能对阳离子的反应性有影响。同时,我们构思并测试了一系列不同大小的反应器(从1到50 cm3),带有单独的隔室,适合与固体电极一起使用(第2章)。 -对于第二种底物(b),我们介绍了用于树型反应的电化学方法:黄原酸酯基团的引入,其消除和自由基加成的引发(第4至8章)。 -在双黄原酸酯存在下通过叔自由基的发电合成黄原酸酯的尝试失败。在Kolbe条件下,后者太容易还原或氧化(第5章)。 -黄原酸酯的阴极还原具有良好的收率,但仅与苯乙酮的衍生物有关。阳极氧化并未导致环化成四氢萘酮(第6章)。 -当使用烷基碘的阴极还原时,通过基团转移在烯烃上引发自由基加成反应失败。但是,当使用具有强电催化活性(Ag,Au,Pd)的阴极进行操作时,我们观察到一个新的反应。它包括将碘乙酸乙酯中的自由基加到伯黄药上,然后环化(第7章)。另外,我们构思并测试了带有继电器的系统,该继电器用于反转电极的极性,以便在吸附抑制电流流动时清洁电极的表面。 -在部分中和的丙二酸的阳极氧化的情况下,引发反应给出了令人鼓舞的结果。但是收率必须进一步提高(收率:45%;校正中间收率:75%)(第8章)。

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    Pulicani Jean-Pierre;

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  • 年度 2013
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  • 原文格式 PDF
  • 正文语种 fr
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