Abstract
N-alkylpyridinium salts are versatile pseudohalides for SET-mediated cross couplings. However, the common 2,4,6-triphenylpyridinium salt is plagued by poor atom economy and high cost of synthesis. Thus, there is a growing need for more practical scaffolds and innovative strategies for pyridinium salt formation. Herein, we report the synthesis of benzylic 2,4,6-collidinium salts via electrooxidative C-H functionalization. This method provides a complementary approach to tradtional strategies relying on substitution and condensation of prefunctionalized substrates.
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