Iashin Vladimir, Berta Dénes, Chernichenko Konstantin, Nieger Martin, Moslova Karina, Pápai Imre, Repo Timo
Department of Chemistry, University of Helsinki, A. I. Virtasen aukio, 1, 00014, Helsinki, Finland.
Institute of Organic Chemistry, Research Centre for Natural Sciences, Magyar tudósok körútja 2, 1117, Budapest, Hungary.
Chemistry. 2020 Nov 2;26(61):13873-13879. doi: 10.1002/chem.202001436. Epub 2020 Sep 29.
Organoboron compounds are essential reagents in modern C-C coupling reactions. Their synthesis via catalytic C-H borylation by main group elements is emerging as a powerful tool alternative to transition metal based catalysis. Herein, a straightforward metal-free synthesis of aryldifluoroboranes from BF and heteroarenes is reported. The reaction is assisted by sterically hindered amines and catalytic amounts of thioureas. According to computational studies the reaction proceeds via frustrated Lewis pair (FLP) mechanism. The obtained aryldifluoroboranes are further stabilized against destructive protodeborylation by converting them to the corresponding air stable tetramethylammonium organotrifluoroborates.
有机硼化合物是现代碳-碳偶联反应中的重要试剂。通过主族元素催化碳-氢键硼化来合成有机硼化合物,正逐渐成为一种强大的工具,可替代基于过渡金属的催化方法。本文报道了一种从BF和杂芳烃直接无金属合成芳基二氟硼烷的方法。该反应由空间位阻胺和催化量的硫脲辅助。根据计算研究,该反应通过受阻路易斯对(FLP)机理进行。通过将所得芳基二氟硼烷转化为相应的空气稳定的四甲基铵有机三氟硼酸盐,可进一步稳定其结构,防止其发生破坏性的原硼化反应。