Huang Xuan, Wang Hongling, Cao Qingxiang, Li Yong, Zhang Junmin
International Joint Research Centre for Molecular Science, College of Chemistry and Environmental Engineering, Shenzhen University Shenzhen 518060 P. R. China
RSC Adv. 2021 May 11;11(28):17320-17323. doi: 10.1039/d1ra02150h. eCollection 2021 May 6.
3,3-Disubstituted oxindoles are important structure motifs in natural products and pharmaceutical agents. Here we disclose a simple and direct access to this class of molecules by using readily available formaldehyde and isatins (and their imines) as the substrates. The reaction proceeds with the assistance of microwave heating in the presence of a mild base. Formaldehyde behaves as both a reductant ( a Cannizzaro process with isatin) and an electrophile.
3,3-二取代氧化吲哚是天然产物和药物制剂中的重要结构基序。在此,我们报道了一种通过使用易得的甲醛和异吲哚酮(及其亚胺)作为底物来简单直接地合成这类分子的方法。该反应在温和碱存在下借助微波加热进行。甲醛既作为还原剂(与异吲哚酮发生坎尼扎罗反应)又作为亲电试剂。