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作 者:Qing Fa Zhou Xue Ping Chu Shen Zhao Tao Lu Wei Fang Tang
机构地区:[1]Department of Organic Chemistry, China Pharmaceutical University, Nanjing 210009, China
出 处:《Chinese Chemical Letters》2012年第6期639-642,共4页中国化学快报(英文版)
基 金:the National Natural Science Foundation of China(No.21102179);Fundamental Research Funds for the Central Universities(No.JKZ2011011) for the financial support
摘 要:An effective method for the synthesis of vinyl thioethers through the conjugate addition of ethanethiol to electron-deficient alkynes promoted by BF3.Et20 has been developed. Electron-deficient internal alkynes react with ethanethiol in this system to yield mainly Z-isomer of vinyl thioether adducts, while electron-deficient terminal alkynes afford mainly E-isomer of vinyl thioether adducts.An effective method for the synthesis of vinyl thioethers through the conjugate addition of ethanethiol to electron-deficient alkynes promoted by BF3.Et20 has been developed. Electron-deficient internal alkynes react with ethanethiol in this system to yield mainly Z-isomer of vinyl thioether adducts, while electron-deficient terminal alkynes afford mainly E-isomer of vinyl thioether adducts.
关 键 词:Vinyl thioether Electron-deficient alkyne Conjugate addition SYNTHESIS
分 类 号:O562.5[理学—原子与分子物理] TQ325.15[理学—物理]
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