ArticleMolecules (Basel, Switzerland)2026
Unusual Chemodivergence in the Amination of 2-Chloro-1,10-Phenanthroline with Di- and Polyamines: Comparison of the Pd-Catalyzed and Catalyst-Free Pathways.
Article in Molecules (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
The amination of 2-chloro-1,10-phenanthroline with various alkylamines and diamines was investigated. The Pd-catalyzed reaction and catalyst-free protocols were shown to lead to different products. Catalyst-free amination of this substrate using aliphatic amines yielded secondary phenanthrolin-2-yl amines in 40-80% yields. The Pd-catalyzed reaction afforded tertiary di(phenanthrolin-2-yl)amines even in the presence of excess amine. This allows for the synthesis of unsymmetric
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