Suppr超能文献

钴催化芳烃的区域选择性硼氢化反应:N-杂环硅烯在金属介导的C-H键活化中作为电子供体

Cobalt-Catalyzed Regioselective Borylation of Arenes: N-Heterocyclic Silylene as an Electron Donor in the Metal-Mediated Activation of C-H Bonds.

作者信息

Ren Hailong, Zhou Yu-Peng, Bai Yunping, Cui Chunming, Driess Matthias

机构信息

State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin, 300071, P. R. China.

Department of Chemistry: Metalorganics and Inorganic Materials Sekr C2, Technische Universität Berlin, Strasse des 17. Juni 135, Berlin, 10623, Germany.

出版信息

Chemistry. 2017 Apr 27;23(24):5663-5667. doi: 10.1002/chem.201605937. Epub 2017 Apr 5.

Abstract

C-H Borylation of arenes has been a subject of great interest recently because of its atom-economy and the wide applicability of borylated products in value-added synthesis. A new bis(silylene)cobalt(II) complex bearing a bis(N-heterocyclic silylene)-pyridine pincer ligand (SiNSi) has been synthesized and structurally characterized. It enabled the regioselective catalytic C-H borylation of pyridines, furans, and fluorinated arenes. Notably, it exhibited complementary regioselectivity for the borylation of fluorinated arenes compared to previously known catalytic systems, demonstrating that N-heterocyclic silylene donors have enormous potential in metal-catalyzed catalytic applications.

摘要

芳烃的碳-氢键硼化反应近来备受关注,因其具有原子经济性以及硼化产物在增值合成中的广泛适用性。一种新型的带有双(N-杂环硅烯)-吡啶钳形配体(SiNSi)的双(硅烯)钴(II)配合物已被合成并进行了结构表征。它能够实现吡啶、呋喃和氟化芳烃的区域选择性催化碳-氢键硼化反应。值得注意的是,与先前已知的催化体系相比,它在氟化芳烃的硼化反应中表现出互补的区域选择性,这表明N-杂环硅烯供体在金属催化应用中具有巨大潜力。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验