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首页> 外文期刊>Scientific reports. >Palladium-catalyzed direct arylation and cyclization of o-iodobiaryls to a library of tetraphenylenes
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Palladium-catalyzed direct arylation and cyclization of o-iodobiaryls to a library of tetraphenylenes

机译:钯催化的直接芳基芳基芳基芳基芳基芳基芳基,对四苯基文库的o-碘扎氏

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Aryl-aryl bond formation constitutes one of the most important subjects in organic synthesis. The recent developments in direct arylation reactions forming aryl-aryl bond have emerged as very attractive alternatives to traditional cross-coupling reactions. Here, we describe a general palladium-catalyzed direct arylation and cyclization of o-iodobiaryls to build a library of tetraphenylenes. This transformation represents one of the very few examples of C-H activation process that involves simultaneous formation of two aryl-aryl bonds. Oxygen plays a vital role by ensuring high reactivity, with air as the promoter furnished the best results. We anticipate this ligand-free and aerobic catalytic system will simplify the synthesis of tetraphenylenes as many of the reported methods involve use of preformed organometallic reagents and will lead to the discovery of highly efficient new direct arylation process.
机译:芳基芳基键形成构成有机合成中最重要的受试者之一。形成芳基芳基键的直接芳基化反应的最新发展已成为传统交叉偶联反应的非常有吸引力的替代品。在这里,我们描述了一种普通钯催化的直接芳基化和O-Iodobiaryl的环化,以构建四苯基文库。该转化是C-H活化过程的少数例子之一,其涉及同时形成两个芳基芳基键。氧气通过确保高反应性,随着促进者提供最佳效果,氧气发挥着重要作用。我们预期这种无氧和有氧催化系统将简化四苯基的合成,因为许多报道的方法涉及使用预先形成的有机金属试剂,并将导致高效的新型直接芳基化过程发现。

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