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Simplifying Iron-Phosphine Catalysts for Cross-Coupling Reactions

机译:简化铁膦催化剂的交叉偶联反应

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摘要

Iron-phosphine complexes are emerging as an excellent choice of catalysts in a range of C—C bond-forming processes. and yet the "rules" for determining selection of the most appropriate phosphine ligands are, at present, far from clear. For example, complexes 1 and 2, which are based on phenylene bis(phosphine) ligands, seem to occupy a privileged position, displaying, to date, unsurpassed performance in the cross-coupling of alkyl halides in terms of the variety of nucleophilic substrates that they tolerate. But are these systems genuinely unique or can simpler catalysts based on cheaper, more widely available bisphosphines be exploited instead? We now show that an understanding of the likely nature of the active catalyst allows the development of far simpler catalysts based on the widely available and inexpensive ligand bis(diphenylphosphino)ethane (dppe).
机译:铁膦配合物正在成为一系列CC键形成过程中的绝佳催化剂选择。然而,目前尚不清楚用于确定选择最合适的膦配体的“规则”。例如,基于亚苯基双(膦)配体的配合物1和2似乎占据了特权地位,迄今为止,在卤代烷的交叉偶联方面,就亲核底物的多样性而言,其表现出了卓越的性能。他们宽容。但是这些系统是真正独特的,还是可以开发基于便宜,应用广泛的双膦的更简单的催化剂呢?现在我们显示出对活性催化剂的可能性质的理解允许基于广泛可获得且便宜的配体双(二苯基膦基)乙烷(dppe)开发更简单的催化剂。

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