Issue 44, 2020

Superelectrophilic Csp3–H bond fluorination of aliphatic amines in superacid: the striking role of ammonium–carbenium dications

Abstract

The superacid-promoted electrophilic Csp3–H bond activation of aliphatic amines generates superelectrophilic species that can be subsequently fluorinated. Demonstrated by low-temperature in situ NMR experiments, the ammonium–carbenium dications, crucial for this reaction, can also react with C–H bonds opening future synthesis perspectives for this mode of activation.

Graphical abstract: Superelectrophilic Csp3–H bond fluorination of aliphatic amines in superacid: the striking role of ammonium–carbenium dications

Supplementary files

Article information

Article type
Communication
Submitted
20 Mar 2020
Accepted
09 Apr 2020
First published
16 Apr 2020

Chem. Commun., 2020,56, 5905-5908

Superelectrophilic Csp3–H bond fluorination of aliphatic amines in superacid: the striking role of ammonium–carbenium dications

M. Artault, N. Mokhtari, T. Cantin, A. Martin-Mingot and S. Thibaudeau, Chem. Commun., 2020, 56, 5905 DOI: 10.1039/D0CC02081H

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