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Chemists Achieve Positional Isomerization of Pyridines via Nitrogen Transposition

Chemists Achieve Positional Isomerization of Pyridines via Nitrogen Transposition

Researchers report a general strategy to interconvert pyridine positional isomers by sequential nitrogen insertion and deletion, enabling N-atom transposition. The method preserves substituent identity across diverse substitution patterns and complex scaffolds, establishing isomerization as a practical synthetic tool.

Original headline

Positional isomerisation of pyridine via nitrogen transposition