Zeng Yu, Yang Shi-Hang, Guo Ji-Lin, Li Yun, Lin Ting, Wang Zhao-Yang
School of Chemistry, South China Normal University, Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, GDMPA Key Laboratory for Process Control and Quality Evaluation of Chiral Pharmaceuticals, Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, Guangzhou 510006, China.
Molecules. 2025 Apr 19;30(8):1832. doi: 10.3390/molecules30081832.
A novel method for the efficient and straightforward synthesis of tetrasubstituted furans is presented, employing a base-catalyzed reaction of -hydroxy ketones and cyano compounds. The reaction proceeds under relatively mild conditions, utilizes readily available starting materials, and exhibits good functional group tolerance and high yields. Notably, this reaction obviates the need for expensive metal catalysts and introduces crucial functional groups such as amino and cyano moieties. Furthermore, it avoids the prerequisite functionalization of substrates, thereby enhancing atomic economy.
本文提出了一种高效、简便地合成四取代呋喃的新方法,该方法采用α-羟基酮与氰基化合物的碱催化反应。该反应在相对温和的条件下进行,使用容易获得的起始原料,具有良好的官能团耐受性和高产率。值得注意的是,该反应无需昂贵的金属催化剂,并引入了关键的官能团,如氨基和氰基部分。此外,它避免了底物的预先官能团化,从而提高了原子经济性。