Issue 54, 2017

SNAr catalysis enhanced by an aromatic donor–acceptor interaction; facile access to chlorinated polyfluoroarenes

Abstract

Selective catalytic SNAr reaction of polyfluoroaryl C–F bonds with chloride is shown. Stoichiometric TMSCl makes the reaction exergonic and allows catalysis, which involves ground state elevation of chloride, aromatic donor–acceptor interactions, and stabilization of the Meisenheimer complex. Traditional cross-coupling of the products is now possible and demonstrates the utility.

Graphical abstract: SNAr catalysis enhanced by an aromatic donor–acceptor interaction; facile access to chlorinated polyfluoroarenes

Supplementary files

Article information

Article type
Communication
Submitted
25 May 2017
Accepted
14 Jun 2017
First published
21 Jun 2017

Chem. Commun., 2017,53, 7545-7548

SNAr catalysis enhanced by an aromatic donor–acceptor interaction; facile access to chlorinated polyfluoroarenes

S. Senaweera and J. D. Weaver, Chem. Commun., 2017, 53, 7545 DOI: 10.1039/C7CC03996D

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