Amination of Phenols and Halophenols via Pyridinium–Iridium Dual Photocatalysis

In this study, we present a photochemical method for the amination of phenols (C–H) and halophenols (SNAr), facilitated by dual catalytic pathways involving both Ir­(III) photocatalysis and phenol–pyridinium electron donor–acceptor complexation. By incorporating a pyridinium additive, we achieved ef...

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Veröffentlicht in:ACS catalysis 2024-08, Vol.14 (16), p.12173-12180
Hauptverfasser: Carson, Matthew C., Liu, Cindy R., Liu, Yaning, Kozlowski, Marisa C.
Format: Artikel
Sprache:eng
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Zusammenfassung:In this study, we present a photochemical method for the amination of phenols (C–H) and halophenols (SNAr), facilitated by dual catalytic pathways involving both Ir­(III) photocatalysis and phenol–pyridinium electron donor–acceptor complexation. By incorporating a pyridinium additive, we achieved efficient C–N coupling between phenols and diverse aromatic nitrogen nucleophiles, delivering high yields (up to 99%) across a wide range of substrates, including pharmaceuticals and natural products. We investigate reaction selectivity and substrate compatibility/limitations through a combination of experimental and computational techniques. Moreover, we highlight the synthetic versatility of the amination products through various late-stage functionalizations including the grafting of two different heteroarenes onto one phenol scaffold.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.4c02797