De Abreu Maxime, Rogge Torben, Lanzi Matteo, Saiegh Tomas J, Houk Kendall N, Wencel-Delord Joanna
Laboratoire d'Innovation Moléculaire et Applications (UMR CNRS 7042), Université de Strasbourg/Université de Haute Alsace, ECPM 25 rue Becquerel, 67087, Strasbourg, France.
Department of Chemistry and Biochemistry, University of California, Los Angeles, California, 90095-1569, USA.
Angew Chem Int Ed Engl. 2024 Apr 15;63(16):e202319960. doi: 10.1002/anie.202319960. Epub 2024 Mar 6.
Regiodivergent reactions are a fascinating tool to rapidly access molecular diversity while using identical coupling partners. We have developed a new approach for regiodivergent synthesis using the dual character of hypervalent bromines. In addition to the recently reported reactivity of hypervalent bromines as aryne precursors, the first transition metal-catalyzed reaction is reported. Accordingly, the development of these two complementary transformations allows for the alteration of regioselectivity to furnish both ortho- and meta-substituted alkynylation products. Mechanistic and computational studies show how these selectivities are controlled.
区域发散反应是一种在使用相同偶联伙伴的同时快速获取分子多样性的迷人工具。我们利用高价溴的双重特性开发了一种区域发散合成的新方法。除了最近报道的高价溴作为芳炔前体的反应性外,还报道了首例过渡金属催化反应。因此,这两种互补转化的发展使得区域选择性得以改变,从而得到邻位和间位取代的炔基化产物。机理和计算研究表明了这些选择性是如何被控制的。