Palladium-Catalyzed Synthesis of Biaryl Ketones via tert-Butyl Isocyanide Insertion
摘要:
A simple and efficient palladium-catalyzed carbonylative Suzuki coupling via tert-butyl isocyanide insertion has been developed, which demonstrates the utility of isocyanides in intermolecular C-C bond construction. This methodology provides a novel pathway for the synthesis of diaryl ketones in moderate to good yields. The approach is tolerant to a wide range of substrates and applicable to library synthesis. A possible reaction mechanism was proposed based on the experimental results.
Palladium-Catalyzed Synthesis of Biaryl Ketones via tert-Butyl Isocyanide Insertion
作者:Yongming Zhu、Zhong Chen、Huaqing Duan、Xiao Jiang、Jinmei Wang、Shilin Yang
DOI:10.1055/s-0033-1341244
日期:——
A simple and efficient palladium-catalyzed carbonylative Suzuki coupling via tert-butyl isocyanide insertion has been developed, which demonstrates the utility of isocyanides in intermolecular C-C bond construction. This methodology provides a novel pathway for the synthesis of diaryl ketones in moderate to good yields. The approach is tolerant to a wide range of substrates and applicable to library synthesis. A possible reaction mechanism was proposed based on the experimental results.