School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK.
Angew Chem Int Ed Engl. 2018 Jan 22;57(4):1082-1086. doi: 10.1002/anie.201711816. Epub 2018 Jan 3.
A new strategy for the coupling of a broad scope of electronically diverse aromatics to boronic esters is reported. The coupling sequence, which relies on the directed ortho-lithiation of chromium arene complexes followed by boronate formation and oxidation, occurs with complete ortho-selectivity and enantiospecificity to give the coupling products in excellent yields and with high functional group tolerance. An intermediate chromium arene boronate complex was characterized by X-ray, NMR, and IR experiments to elucidate the reaction mechanism.
报道了一种将广泛电子差异的芳烃与硼酸酯偶联的新策略。该偶联序列依赖于铬芳烃配合物的定向邻位锂化,随后进行硼酸酯形成和氧化,具有完全的邻位选择性和对映选择性,以优异的收率和高官能团容忍度得到偶联产物。通过 X 射线、NMR 和 IR 实验对中间铬芳烃硼酸酯配合物进行了表征,以阐明反应机理。