废止
化学
区域选择性
催化作用
铑
阳离子聚合
组合化学
溶剂
药物化学
有机化学
作者
Jiajie Li,Xin Xu,Zhenli Luo,Zhen Yao,Ji Yang,Xin Zhang,Lijin Xu,Peng Wang,Qian Shi
标识
DOI:10.1002/adsc.202101489
摘要
Abstract Cp*Rh(III)‐catalyzed regioselective C−H annulation and alkenylation of 2‐pyridones with terminal alkynes have been developed. The cationic Cp*Rh(III) catalytic system containing FeCl 3 additive enables annulation of 1‐(2‐pyridyl)‐2‐pyridones with terminal alkynes, providing efficient access to 5,7‐diarylated 2‐quinolinones. The reaction pathway can be switched to alkenylation with [Cp*RhCl 2 ] 2 as the catalyst, NaOAc as the additive and HOAc as the solvent, affording C6‐alkenylated 1‐(2‐pyridyl)‐2‐pyridones in high yields. These protocols accommodate a wide range of substrates with good functional group compatibility. magnified image
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