Demonstrates a novel method for synthesizing pyridyl ligands, suggesting improved applications in catalysis.
Pyridyl motifs equipped with N ‐substituents can be powerful ligands for catalysis, yet their broader adoption is limited by the lack of a practical method to prepare these scaffolds. We report a modular, robust, and versatile Buchwald–Hartwig amination protocol that enables the rapid synthesis of bipyridine, phenanthroline, terpyridine, and pybox ligands bearing dialkylamine, diarylamine, and heteroaromatic N ‐substituents. These conditions streamline ligand library synthesis and will facilitate systematic studies in catalysis and related applications.
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Petrik et al. (2026) studied this question.
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