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Multimetallic Catalysis Enabled Cross-Coupling of Aryl Bromides with Aryl Triflates

机译:多金属催化实现芳基溴化物与芳基三氟甲磺酸酯的交叉偶联

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摘要

Transition metal-catalyzed strategies for the formation of new C-C bonds have revolutionized the field of organic chemistry, enabling the efficient synthesis of ligands, materials, and biologically active molecules. In cases where a single metal fails to promote a selective or efficient transformation, the synergistic cooperation of two distinct catalysts – multimetallic catalysis – can be employed instead. Many important reactions rely on multimetallic catalysis, including the Wacker oxidation of olefins and the Sonogashira coupling of alkynes with aryl halides. However, the application of this strategy, even in recently developed methods, has largely been limited to the use of metals with distinct reactivities, with only one metal catalyst undergoing an oxidative addition. In this manuscript, we demonstrate that cooperativity between two d10 metal catalysts, (bipyridine)nickel and (1,3-bis(diphenylphosphino)propane)palladium, enables a general cross-Ullman reaction. Our method couples aryl bromides with aryl triflates directly, eliminating the use of arylmetal reagents and avoiding the challenge of differentiating between multiple C–H bonds that is required for many C–H activation methods. The selectivity does not require an excess of either substrate and originates from the orthogonal activity of the two catalysts and the relative stability of the two arylmetal intermediates. While (dppp)Pd reacts preferentially with aryl triflates to afford a persistent intermediate, (bpy)Ni reacts preferentially with aryl bromides to form a transient, reactive intermediate. Although each catalyst forms less than 5% cross product in isolation, together they are able to achieve up to 94% yield. Our results reveal a new, general method for the synthesis of biaryls, heteroaryls, and dienes, as well as a new mechanism for selective transmetalation between two catalysts. We anticipate that this reaction will simplify the synthesis of pharmaceutical agents, many of which are currently made with pre-formed organometallic reagents, and lead to the discovery of new multimetallic reactions.
机译:过渡金属催化形成新CC键的策略彻底改变了有机化学领域,实现了配体,材料和生物活性分子的有效合成。为了促进选择性或有效转化,可以使用两种不同催化剂(多金属催化)的协同合作 。许多重要的反应都依赖于多金属催化, 包括烯烃的Wacker氧化以及炔烃与芳基卤化物的Sonogashira偶联。即使在最近开发的方法 中,该策略的应用在很大程度上也仅限于使用具有不同反应性的金属,只有一种金属催化剂会进行氧化加成。 手稿中,我们证明了两种d10金属催化剂(联吡啶)镍和(1,3-双(二苯基膦基)丙烷)钯之间的协同作用使一般的跨乌尔曼反应成为可能。我们的方法偶联芳基溴与芳基三氟甲磺酸酯直接反应,消除了芳基金属试剂的使用,避免了许多C–H活化方法所需的区分多个C–H键的挑战。选择性不需要过多任一底物的分子,并且源自两个分子的正交活性催化剂和两种芳基金属中间体的相对稳定性。 (dppp)Pd优先与芳基三氟甲磺酸酯反应生成持久性中间体,而(bpy)Ni优先与芳基溴化物反应形成瞬态活性中间体。尽管每种催化剂孤立地形成少于5%的交叉产物,但是它们一起可以实现高达94%的产率。我们的结果揭示了一种新的合成联芳基,杂芳基和二烯的通用方法,以及在两种催化剂之间进行选择性过渡金属化的新机理。我们预计该反应将简化药物的合成,目前许多药物是由预先形成的有机金属试剂制备的,从而导致新的多金属反应的发现。

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