Berichtigung: Radical 1,4/5‐Amino Shift Enables Access to Fluoroalkyl‐Containing Primary β(γ)‐Aminoketones under Metal‐Free Conditions.

Keywords: amino migration; fluoroalkylamination; ketoxime ethers; radical rearrangement; synthetic methods EN amino migration fluoroalkylamination ketoxime ethers radical rearrangement synthetic methods 26224 26224 1 12/01/21 20211206 NES 211206 The authors wish to correct three product structures in their Communication. GRAPH The reaction of ketoxime ethers B 1ag b - B 1ai b first delivered linear -aminoketone hydrochlorides (the original structures), which can spontaneously undergo condensation to form cyclic imine hydrochlorides. The three structures ( B 2ag b - B 2ai b ) in Table 2, which were originally identified as -aminoketone hydrochlorides, are actually their intramolecular dehydrated condensation derivative hydrochlorides. [Extracted from the article]