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Beilstein J. Org. Chem. 2026, 22, 925–947, doi:10.3762/bjoc.22.73
Graphical Abstract
Scheme 1: Mechanistic pathways in copper-catalyzed hydroamination.
Scheme 2: Synthesis of copper–amido complexes.
Scheme 3: Cu–amido catalysts studied for the aza-Michael addition of aniline to electron-deficient olefins.
Scheme 4: Copper-catalyzed aza-Michael addition of (hetero)aromatic amines to α,β-unsaturated alkenes.
Scheme 5: Copper-catalyzed 1,6-conjugate addition of aza-heterocycles to sulfonyl dienes.
Scheme 6: Cu-catalyzed aza-Michael addition of arylamines to allylic sulfones.
Scheme 7: Cyclic(alkyl)(amino)carbene-copper-catalyzed aza-Michael addition.
Scheme 8: Aza-Michael addition enabled by Lewis acidic copper catalyst. a20 mol % bpy, 50 mol % Na2CO3.
Scheme 9: One-pot cyclization via aza-Michael addition enabled by Lewis acidic copper catalyst.
Scheme 10: Lewis acidic Cu-catalyzed tandem reaction via aza-Michael addition.
Scheme 11: Copper nanomaterials-catalyzed aza-Michael addition via Lewis acid activation and radical pathways.
Scheme 12: Copper–amido-mediated hydroamination of aniline with vinylarenes.
Scheme 13: Copper-catalyzed anti-Markovnikov hydroamination of (hetero)aromatic N–H with vinylarenes.
Scheme 14: Hydroamination of oxa- and azabenzonorbornadienes with pyrazoles.
Scheme 15: Copper-catalyzed enantioselective hydroamination of cyclopropenes with pyrazoles.
Scheme 16: Copper/Brønsted acid system for hydroamination of strained alkenes.
Scheme 17: Hydroamination of allenes enabled by Lewis acidic copper catalyst.
Scheme 18: Enantioselective intramolecular hydroamination through aminocupration followed by radical processes....
Scheme 19: Visible-light-induced copper-catalyzed hydroamination of styrenes.
Scheme 20: Lewis acid-catalyzed radical hydroamination of styrenes with isatins.