Abstract
The regioselective lithiation of 1,2,3-triazoles provides an opportunity to introduce additional functionality, however this simple functionalisation strategy using triazoles bearing electron-withdrawing N-substituents has not been investigated until now. Herein, we demonstrate that the lithiated triazole intermediates can readily decompose, even at −78 °C. In addition, lithiation-deuteration studies reveal lithiation can take place competitively on both the triazole and the electron-withdrawn aryl ring. Careful control of reaction conditions is therefore required to i) minimise decomposition pathways; and ii) facilitate regioselective functionalisation of the triazole.
Supplementary materials
Title
Supporting Information
Description
All experimental details are provided in the supporting information, including details on i) reaction set-up and work-up; ii) analytical characterisation data, including melting points, 1H, 2H, 13C and 19F NMR spectroscopy, IR spectroscopy and high-resolution mass spectrometry; and iii) NMR traces for all novel compounds.
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