Literature DB >> 29047192

Palladium-Catalyzed Cross-Coupling of Nitroarenes.

Yang Yang1.   

Abstract

Pd at the crossroads: The palladium-catalyzed cross-coupling of nitroarenes has eluded chemists for decades. Recently, the first palladium-catalyzed Suzuki-Miyaura and Buchwald-Hartwig cross-couplings of nitroarenes were reported. Mechanistically, this process involves the challenging oxidative addition of LPd0 into the Ar-NO2 bond. This process features a broad substrate scope with respect to both the nitroarene and the nucleophilic coupling partners.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  aromatic substitution; copper; cross-coupling; palladium; sustainable chemistry

Year:  2017        PMID: 29047192     DOI: 10.1002/anie.201708940

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  3 in total

1.  A methylation platform of unconventional inert aryl electrophiles: trimethylboroxine as a universal methylating reagent.

Authors:  Boya Feng; Yudong Yang; Jingsong You
Journal:  Chem Sci       Date:  2020-05-25       Impact factor: 9.825

2.  Advances in Cross-Coupling Reactions.

Authors:  José Pérez Sestelo; Luis A Sarandeses
Journal:  Molecules       Date:  2020-10-01       Impact factor: 4.411

3.  A Walk through Recent Nitro Chemistry Advances.

Authors:  Nagatoshi Nishiwaki
Journal:  Molecules       Date:  2020-08-12       Impact factor: 4.411

  3 in total

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