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Gold(I)-mediated thiourea organocatalyst activation: A synergic effect for asymmetric catalysis

机译:金(I)介导的硫脲有机催化剂活化:不对称催化的协同作用

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摘要

Several group 11 metal complexes with chiral thiourea organocatalysts have been prepared and tested as organocatalysts. The promising results on the influence of metal-assisted thiourea organocatalysts in the asymmetric Friedel–Crafts alkylation of indole with nitrostyrene are described. Better results with the metal complexes have been achieved because of the cooperative effects between the chiral thiourea and the metal. The synergic effect between both species is higher than the effect promoted by each one separately, especially for gold(I). These outcomes are attributed to a pioneering gold(I) activation of the thiourea catalysts, affording a more acidic and rigid catalytic complex than that provided by the thiourea alone. Furthermore, the use of the gold–thiourea organocatalyst allows reducing the catalyst loading to 1–3 mol %. This contribution could become an important starting point for further investigations opening a new line of research overlooked so far in the literature.
机译:已经制备了几种具有手性硫脲有机催化剂的11族金属配合物,并作为有机催化剂进行了测试。描述了金属辅助硫脲有机催化剂对吲哚与硝基苯乙烯的不对称Friedel-Crafts烷基化反应的影响的令人鼓舞的结果。由于手性硫脲与金属之间的协同作用,金属配合物获得了更好的结果。两种物质之间的协同作用高于各自促进的协同作用,尤其是对于金(I)。这些结果归因于硫脲催化剂的开创性金(I)活化,比单独使用硫脲提供的酸性和刚性催化复合物更为酸性和刚性。此外,使用金-硫脲有机催化剂可将催化剂负载量降低至1-3 mol%。这一贡献可能会成为进一步研究的重要起点,以进行新的研究,从而开辟迄今为止在文献中被忽视的研究领域。

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