Publication: Nickel‐Catalyzed Asymmetric Synthesis of α‐Arylbenzamides
Nickel‐Catalyzed Asymmetric Synthesis of α‐Arylbenzamides
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Cuesta‐Galisteo, S., Schörgenhumer, J., Wei, X., Merino, E., & Nevado, C. (2021). Nickel‐Catalyzed Asymmetric Synthesis of α‐Arylbenzamides. Angewandte Chemie Internationale Edition, 60(3), 1605–1609. https://doi.org/10.1002/anie.202011342
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A nickel‐catalyzed asymmetric reductive hydroarylation of vinyl amides to produce enantioenriched α‐arylbenzamides is reported. The use of a chiral bisimidazoline (BIm) ligand, in combination with diethoxymethylsilane and aryl halides, enables the regioselective introduction of aryl groups to the internal position of the olefin, forging a new stereogenic center α to the N atom. The use of neutral reagents and mild reaction conditions provides simple access to pharmacologically relevant motifs present in anticancer, SARS‐CoV PLpro inhi
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Cuesta‐Galisteo, S., Schörgenhumer, J., Wei, X., Merino, E., & Nevado, C. (2021). Nickel‐Catalyzed Asymmetric Synthesis of α‐Arylbenzamides. Angewandte Chemie Internationale Edition, 60(3), 1605–1609. https://doi.org/10.1002/anie.202011342