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Copper-catalyzed, ceric ammonium nitrate mediated N-arylation of amines†
Uma Maheshwar Gonela,Seth Y. Ablordeppey
New Journal of Chemistry Pub Date : 01/17/2019 00:00:00 , DOI:10.1039/C8NJ06145A
Abstract

Cu-Catalyzed, ligand- and base-free cross-coupling of aryl boronic acids with primary and secondary amines has been reported. This ‘Chan–Evans–Lam’ reaction has revealed that at room temperature, with a catalytic amount of copper(II) acetate and ceric ammonium nitrate (CAN) as an oxidant, N-arylation can result in an effective C–N bond formation. This air stable, practical, robust protocol enables tolerance towards a variety of functional groups on both boronic acid and amine partners.

Graphical abstract: Copper-catalyzed, ceric ammonium nitrate mediated N-arylation of amines
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