Issue 75, 2020

Evidence and exploitation of dicationic ammonium–nitrilium superelectrophiles: direct synthesis of unsaturated piperidinones

Abstract

Exploiting superacid activation, the reactivity of aminonitriles was enhanced through the transient formation of highly reactive ammonium–nitrilium superelectrophiles. Demonstrated by using in situ low-temperature NMR experiments and confirmed by X-ray diffraction analysis, these dications can be intramolecularly trapped by non-activated alkenes to generate unsaturated piperidinones, including enantioenriched ones, in a straightforward way.

Graphical abstract: Evidence and exploitation of dicationic ammonium–nitrilium superelectrophiles: direct synthesis of unsaturated piperidinones

Supplementary files

Article information

Article type
Communication
Submitted
22 Apr 2020
Accepted
30 Jul 2020
First published
05 Aug 2020

Chem. Commun., 2020,56, 11110-11113

Evidence and exploitation of dicationic ammonium–nitrilium superelectrophiles: direct synthesis of unsaturated piperidinones

T. Cantin, Y. Morgenstern, A. Mingot, A. Kornath and S. Thibaudeau, Chem. Commun., 2020, 56, 11110 DOI: 10.1039/D0CC02910F

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