CuBr-Catalyzed Reaction of N , N -Dimethylanilines and Silyl Enol Ethers: An Alternative Route to β-Arylamino Ketones
Lehao Huang, Xunbin Zhang, Yuhong Zhang
Abstract
Lehao Huang, Xunbin Zhang, Yuhong Zhang
Abstract
A wide range of silyl enol ethers undergo the reactions with N,N-dimethylanilines in the presence of transition metal catalysts under mild conditions to give beta-arylamino ketones. In the cases of silyl enol ethers derived from unsymmetrical ketones, regiospecific addition of carbonyl compounds was obtained at the olefinic position of silyl enol ether.
OpenAlex reports 69 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
A wide range of silyl enol ethers undergo the reactions with N,N-dimethylanilines in the presence of transition metal catalysts under mild conditions to give beta-arylamino ketones. In the cases of silyl enol ethers derived from unsymmetrical ketones, regiospecific addition of carbonyl compounds was obtained at the olefinic position of silyl enol ether.
Key concepts: Silylation, Enol, Chemistry, Silyl enol ether, Catalysis, Enol ether, Silyl ether, Medicinal chemistry