Department of Chemistry, The University of Texas at San Antonio, One UTSA Circle, San Antonio, TX, 78249, USA.
Angew Chem Int Ed Engl. 2020 May 11;59(20):7921-7927. doi: 10.1002/anie.201916710. Epub 2020 Mar 17.
The development of efficient and selective C-N bond-forming reactions from abundant feedstock chemicals remains a central theme in organic chemistry owing to the key roles of amines in synthesis, drug discovery, and materials science. Herein, we present a dual catalytic system for the N-alkylation of diverse aromatic carbocyclic and heterocyclic amines directly with carboxylic acids, by-passing their preactivation as redox-active esters. The reaction, which is enabled by visible-light-driven, acridine-catalyzed decarboxylation, provides access to N-alkylated secondary and tertiary anilines and N-heterocycles. Additional examples, including double alkylation, the installation of metabolically robust deuterated methyl groups, and tandem ring formation, further demonstrate the potential of the direct decarboxylative alkylation (DDA) reaction.
由于胺在合成、药物发现和材料科学中的关键作用,从丰富的原料化学品中开发高效和选择性的 C-N 键形成反应仍然是有机化学的一个核心主题。在此,我们提出了一种双催化体系,用于直接用羧酸对各种芳族碳环和杂环胺进行 N-烷基化,绕过其作为氧化还原活性酯的预活化。该反应由可见光驱动、吖啶催化的脱羧作用引发,可获得 N-烷基化的仲胺和叔胺以及 N-杂环。其他实例,包括双烷基化、安装代谢稳定的氘代甲基以及串联环形成,进一步证明了直接脱羧烷基化(DDA)反应的潜力。