Brønsted acid-catalyzed α-halogenation of ynamides from halogenated solvents and pyridine-N-oxides.

The keteniminium ions generated from the protonation of ynamides formed reversible adducts with counter anions and pyridine-N-oxides as well as halogenated solvents. Above 80 °C, the halonium ions selectively undergo a rate-limiting attack by pyridine-N-oxides, leading to (E)-haloenamides in good yields. [ABSTRACT FROM AUTHOR]