63255-43-6Relevant academic research and scientific papers
Transition-Metal-Free Aminoacylation of Ynones with Amides: Synthesis of 3-Carbonyl-4-quinolinones or Functionalized Enaminones
Zheng, Zhong,Tao, Qihai,Ao, Yujuan,Xu, Murong,Li, Yanzhong
, p. 3907 - 3910 (2018)
A transition-metal-free tandem process for the synthesis of substituted quinolin-4(1H)-ones or enaminones is presented. A base-promoted insertion of ynones into the C-N σ-bond of amides is the key step in this process, which provides the corresponding aminoacylation products in good to high yields. Quinolin-4(1H)-ones are selectively formed via the subsequent N-cyclization pathway in the cases of ynones bearing an ortho-bromo-substituted aryl ring. Easily accessible starting materials and high atom economy make this procedure attractive.
