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Indirect Electrochemical Cyclisation of Bromoalkoxylated Derivatives using Environmentally Friendly Methodologies

机译:使用环保方法的溴烷氧基化衍生物间接电化学环化

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The electrochemical intramolecular cyclization of bromoalkoxylated derivatives 1 using Ni(ll) complex as mediator of electron transfer was carried out in ethanol by constant-current electrolysis in one-compartment cell in the absence of sacrificial anodes as an environmentally friendly systems. It is demonstrated that the electroreduction reaction of bromoalkoxylated derivatives was catalyzed by the electrogenerated Ni(I) complexes. Only cyclization to the five-membered-ring esters was obtained in moderate to good yields as the main products. Functionalyzed tetrahydrofurans are important intermediates in the synthesis of natural products such as lignans. A mechanistic scheme is proposed to explain the results obtained by means of cyclic voltammetry and constant-current electrolysis.
机译:使用Ni(L1)复合物作为电子转移介质的溴代烷氧基化衍生物1的电化学分子内环化在乙醇中通过单室细胞中的恒定电流在没有牺牲阳极作为环保系统的情况下在乙醇中进行。证明溴烷氧基化衍生物的电控反应通过电化的Ni(I)配合物催化。仅在中等至良好的产率作为主要产品中获得对五元环酯的环化。功能统计学的四氢呋喃是合成天然产物如木质素的重要中间体。提出了一种机械方案来解释通过循环伏安法和恒流电解获得的结果。

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