| Literature DB >> 32162451 |
Ryan T McGuire1, Connor M Simon1, Arun A Yadav2, Michael J Ferguson3, Mark Stradiotto1.
Abstract
The development of Ni-catalyzed C-N cross-couplings of sulfonamides with (hetero)aryl chlorides is reported. These transformations, which were previously achievable only with Pd catalysis, are enabled by use of air-stable (L)NiCl(o-tol) pre-catalysts (L=PhPAd-DalPhos and PAd2-DalPhos), without photocatalysis. The collective scope of (pseudo)halide electrophiles (X=Cl, Br, I, OTs, and OC(O)NEt2 ) demonstrated herein is unprecedented for any reported catalyst system for sulfonamide C-N cross-coupling (Pd, Cu, Ni, or other). Preliminary competition experiments and relevant coordination chemistry studies are also presented.Entities:
Keywords: amination; cross-coupling; ligand design; nickel; sulfonamides
Year: 2020 PMID: 32162451 DOI: 10.1002/anie.202002392
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336