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Visible-Light-Induced Photoreductive Generation of Radicals from Epoxides and Aziridines

机译:可见光诱导的环氧和氮丙啶基自由基的光还原生成

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As a result of its unique features, radical chemistry has become a reliable and efficient tool for synthetic chemists over the last fifty years. Nowadays, the necessity to devise ecocompatible alternatives for the generation of radical species has stimulated intense research efforts. The development of single-electron transfer (SET) redox processes using catalytic amounts of metal complexes would be a significant advance. For that purpose, the use of visible light and a photoredox catalyst such as [Ru(bpy)3]Cl2 has lately appeared to offer very promising possibilities. Thus, following the pioneering findings of Cano-Yelo and Deronzier, recent contributions from the research groups of Yoon, MacMillan, and Stephenson have demonstrated that enones, perfluorated iodides, as well as activated chlorides and bromides are suitable substrates for the formation of radicals by visible light-catalyzed reductive electron transfers.
机译:由于其独特的功能,在过去的五十年中,自由基化学已成为合成化学家可靠且有效的工具。如今,有必要设计出生态兼容的替代品来生产自由基物种,这刺激了人们的大量研究工作。利用催化量的金属络合物开发单电子转移(SET)氧化还原工艺将是一项重大进步。为此,近来看来使用可见光和光氧化还原催化剂例如[Ru(bpy)3] Cl 2提供了非常有前途的可能性。因此,继Cano-Yelo和Deronzier的开创性发现之后,Yoon,MacMillan和Stephenson研究小组的最新成果表明,烯酮,全氟碘化物以及活化的氯化物和溴化物是形成自由基的合适底物。可见光催化的还原电子转移。

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