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Ag 催化的丙二酸衍生物的选择性脱羧单氟和二氟化反应。

Ag-Catalyzed Chemoselective Decarboxylative Mono- and gem-Difluorination of Malonic Acid Derivatives.

机构信息

Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering , Nanjing Tech University , Nanjing 211816 , China.

出版信息

J Am Chem Soc. 2019 Apr 10;141(14):5617-5622. doi: 10.1021/jacs.9b00681. Epub 2019 Mar 28.

Abstract

Malonic acid derivatives have been successfully applied in a Ag-catalyzed decarboxylative fluorination reaction, providing an unprecedented route to either gem-difluoroalkanes or α-fluorocarboxylic acids by the judicious selection of base and solvent. This reaction features the use of readily available starting materials, tunable chemoselectivity and good functional group compatibility as well as gram-scale synthetic capability. The advantage of using malonic acid derivatives in this radical decarboxylative functionalization is further highlighted by the facile transformations of the α-fluorocarboxylic acid to valuable fluorine-containing compounds. Preliminary mechanistic studies suggest that an α-carboxylic acid radical is involved in this reaction.

摘要

丙二酸衍生物已成功应用于 Ag 催化的脱羧氟化反应中,通过合理选择碱和溶剂,为提供全氟烷烃或α-氟羧酸提供了一条前所未有的途径。该反应具有使用易得的起始原料、可调的化学选择性和良好的官能团兼容性以及克级合成能力等优点。通过α-氟羧酸容易转化为有价值的含氟化合物,进一步突出了在这种自由基脱羧官能化中使用丙二酸衍生物的优势。初步的机理研究表明,反应中涉及α-羧酸自由基。

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