1025784-76-2Relevant academic research and scientific papers
Copper-promoted Chan-Lam coupling between enaminones and aryl boronic acids
Duan, Xiyan,Liu, Ning,Liu, Kun,Song, Yakun,Wang, Jia,Mao, Xianhua,Xu, Weidong,Yang, Shijie,Li, Huixian,Ma, Junying
supporting information, p. 4187 - 4190 (2018/10/24)
A novel copper-promoted N-arylation of enaminones with aromatic boronic acids has been developed, which provides an efficient way to synthesize N-aryl enaminones with a broad substrate scope and excellent functional group compatibility. The N-aryl enaminones could be converted into a series of highly valuable building blocks and bioactive compounds. Notably, in comparison with traditional methods, this alternative approach provides accesses to N-aryl enaminones bearing multiple aromatic rings.
Simple and efficient one-pot, three-component, solvent-free synthesis of β-enaminones via sonogashira coupling-michael addition sequences
Palimkar, Sanjay S.,More, Vijaykumar S.,Srinivasan, Kumar V.
, p. 1456 - 1469 (2008/09/21)
A simple, efficient, and environmentally friendly one-pot, three-component synthesis of β-enaminones via Sonogashira coupling-Michael addition sequences under solvent-free conditions has been reported. Also the synthesis of β-enaminones has been achieved
