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Pd(ii)-Catalyzed C8-H alkoxycarbonylmethylation of 1-naphthylamides with α-chloroalkyl esters
Xiaolong Wang1, Cancan Feng, Fan Yang
1The College of Chemistry and Molecular Engineering, Henan Key Laboratory of Chemical Biology and Organic Chemistry, Key Laboratory of Applied Chemistry of Henan Universities, Zhengzhou University, Zhengzhou, PR China. yangf@zzu.edu.cn wyj@zzu.edu.cn.
Abstract:
An efficient protocol for palladium-catalyzed picolinamide directed C8-H alkoxycarbonylmethylation of 1-naphthylamine derivatives with α-chloroalkyl esters has been developed. The reaction exhibited a broad substrate scope and good functional group tolerance with high isolated yields. Note that α-chloroalkyl esters as a new type of alkylating reagent could be easily functionalized further due to their pending an ester group.
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