Li Li-Jing, Wei Yi, Zhao Yu-Lian, Gao Yang, Hu Xiao-Qiang
Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science, School of Chemistry and Materials Science, South-Central Minzu University, Wuhan 430074, China.
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China.
Org Lett. 2024 Feb 9;26(5):1110-1115. doi: 10.1021/acs.orglett.3c04395. Epub 2024 Jan 26.
Despite the significant success of decarboxylative radical reactions, the catalytic systems vary considerably upon different radical acceptors, requiring renewed case-by-case reaction optimization. Herein, we developed an iron catalytic condition that enables the highly efficient decarboxylation of various carboxylic acids for a range of radical transformations. This operationally simple protocol was amenable to a wide array of radical acceptors, delivering structurally diverse oxime ethers, alkenylation, alkynylation, thiolation, and amidation products in useful to excellent yields (>40 examples, up to 95% yield).
尽管脱羧自由基反应取得了显著成功,但催化体系因不同的自由基受体而有很大差异,需要针对具体反应逐一重新进行优化。在此,我们开发了一种铁催化条件,能够使各种羧酸高效脱羧,用于一系列自由基转化反应。这种操作简单的方法适用于多种自由基受体,能以良好至优异的产率(>40个实例,高达95%产率)得到结构多样的肟醚、烯基化、炔基化、硫醇化和酰胺化产物。