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Cu-Catalyzed/mediated synthesis of N-fluoroalkylanilines from arylboronic acids: fluorine effect on the reactivity of fluoroalkylamines†
Hui Wang,Yuan-Hong Tu,De-Yong Liu,Xiang-Guo Hu
Organic & Biomolecular Chemistry Pub Date : 08/03/2018 00:00:00 , DOI:10.1039/C8OB01581C
Abstract

An oxidative coupling reaction of fluoroalkylamines with arylboronic acids has been achieved for the first time. Fluorine has profound influence on the reactivity and fluoroalkylated amines have the following reactivity trend: difluoroethylamine > trifluoroethylamine > pentafluoropropylamine ≈ heptafluorobutylamine.

Graphical abstract: Cu-Catalyzed/mediated synthesis of N-fluoroalkylanilines from arylboronic acids: fluorine effect on the reactivity of fluoroalkylamines
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