ArticleJournal of the American Chemical Society2024
Cu-Catalyzed Amination of Base-Sensitive Aryl Bromides and the Chemoselective N- and O-Arylation of Amino Alcohols.
Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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Who cites it
11 citing papers in PubMed.
- Base-Free C-N Cross-Electrophile Coupling.Journal of the American Chemical Society · 2026Article
- An insight into the synthetic routes for N-arylation of morpholine using metal-catalyzed and metal-free methods.Molecular diversity · 2026Review
- On the Structure and Redox Behavior of Ni and Cu Single Atoms Supported on Carbon Nitride.Angewandte Chemie (International ed. in English) · 2026Article
- Stereospecific alkenylation of carboranes: copper-catalyzed access to pyridylcarboranyl alkenes.Chemical science · 2026Article
- Ligand Design Enables Cu-Catalyzed Etherification of Aryl Bromides Using Mild Bases.Organic letters · 2026Article
- Development of a Ligand for Cu-Catalyzed Amination of Base-Sensitive (Hetero)aryl Chlorides.Journal of the American Chemical Society · 2025Article
- General method for carbon-heteroatom cross-coupling reactions via semiheterogeneous red-light metallaphotocatalysis.Nature communications · 2025Article
- Efficient Aminations of Aryl Halides by a Cu(II) Catalyst.Journal of the American Chemical Society · 2025Article
- Assembly of (hetero)aryl sulfilimines via copper-catalyzed enantioselective S-arylation of sulfenamides with (hetero)aryl Iodides.Nature communications · 2025Article
- Cross-Coupling Reactions with Nickel, Visible Light, andACS catalysis · 2025Article
- Copper-Catalyzed Amination of Aryl Chlorides under Mild Reaction Conditions.Journal of the American Chemical Society · 2024Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
We report a general and functional-group-tolerant method for the Cu-catalyzed amination of base-sensitive aryl bromides including substrates possessing acidic functional groups and small five-membered heteroarenes. The results presented herein substantially expand the scope of Cu-catalyzed C-N coupling reactions. The combination of
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Registered trials
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