2009Organic LettersRequires access

CuBr-Catalyzed Reaction of N , N -Dimethylanilines and Silyl Enol Ethers: An Alternative Route to β-Arylamino Ketones

Lehao Huang, Xunbin Zhang, Yuhong Zhang

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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.

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What this paper is about

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.

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OpenAlex reports 69 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available 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.

Key concepts: Silylation, Enol, Chemistry, Silyl enol ether, Catalysis, Enol ether, Silyl ether, Medicinal chemistry

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CuBr-Catalyzed Reaction of N , N -Dimethylanilines and Silyl Enol Ethers: An Alternative Route to β-Arylamino Ketones — Research Paper | ScholarLens