Literature DB >> 32162451

Nickel-Catalyzed Cross-Coupling of Sulfonamides With (Hetero)aryl Chlorides.

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.
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  2 in total

1.  Photochemically Mediated Nickel-Catalyzed Synthesis of N-(Hetero)aryl Sulfamides.

Authors:  R Thomas Simons; Georgia E Scott; Anastasia Gant Kanegusuku; Jennifer L Roizen
Journal:  J Org Chem       Date:  2020-05-04       Impact factor: 4.354

2.  A simple and efficient copper-catalyzed three-component reaction to synthesize (Z)-1,2-dihydro-2-iminoquinolines.

Authors:  Xiai Luo; Yu Zhao; Susu Tao; Zhong-Tao Yang; Hui Luo; Weiguang Yang
Journal:  RSC Adv       Date:  2021-09-29       Impact factor: 4.036

  2 in total

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