Literature DB >> 26360330

Comparison of dppf-Supported Nickel Precatalysts for the Suzuki-Miyaura Reaction: The Observation and Activity of Nickel(I).

Louise M Guard1, Megan Mohadjer Beromi1, Gary W Brudvig1, Nilay Hazari2, David J Vinyard1.   

Abstract

Ni-based precatalysts for the Suzuki-Miyaura reaction have potential chemical and economic advantages compared to commonly used Pd systems. Here, we compare Ni precatalysts for the Suzuki-Miyaura reaction supported by the dppf ligand in 3 oxidation states, 0, I and II. Surprisingly, at 80 °C they give similar catalytic activity, with all systems generating significant amounts of Ni(I) during the reaction. At room temperature a readily accessible bench-stable Ni(II) precatalyst is highly active and can couple synthetically important heterocyclic substrates. Our work conclusively establishes that Ni(I) species are relevant in reactions typically proposed to involve exclusively Ni(0) and Ni(II) complexes.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Suzuki-Miyaura coupling; cross-coupling; homogeneous catalysis; nickel; reaction mechanism

Year:  2015        PMID: 26360330     DOI: 10.1002/anie.201505699

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


  10 in total

1.  Well-defined nickel and palladium precatalysts for cross-coupling.

Authors:  Nilay Hazari; Patrick R Melvin; Megan Mohadjer Beromi
Journal:  Nat Rev Chem       Date:  2017-03-01       Impact factor: 34.035

2.  Modifications to the Aryl Group of dppf-Ligated Ni σ‑Aryl Precatalysts: Impact on Speciation and Catalytic Activity in Suzuki-Miyaura Coupling Reactions.

Authors:  Megan Mohadjer Beromi; Gourab Banerjee; Gary W Brudvig; David J Charboneau; Nilay Hazari; Hannah M C Lant; Brandon Q Mercado
Journal:  Organometallics       Date:  2018-10-16       Impact factor: 3.876

3.  Development of an Improved System for the Carboxylation of Aryl Halides through Mechanistic Studies.

Authors:  David J Charboneau; Gary W Brudvig; Nilay Hazari; Hannah M C Lant; Andrew K Saydjari
Journal:  ACS Catal       Date:  2019-03-14       Impact factor: 13.084

Review 4.  Homogeneous Organic Electron Donors in Nickel-Catalyzed Reductive Transformations.

Authors:  David J Charboneau; Nilay Hazari; Haotian Huang; Mycah R Uehling; Susan L Zultanski
Journal:  J Org Chem       Date:  2022-06-07       Impact factor: 4.198

5.  Nickel(I) Aryl Species: Synthesis, Properties, and Catalytic Activity.

Authors:  Megan Mohadjer Beromi; Gourab Banerjee; Gary W Brudvig; Nilay Hazari; Brandon Q Mercado
Journal:  ACS Catal       Date:  2018-02-13       Impact factor: 13.084

6.  Identification of the Active Catalyst for Nickel-Catalyzed Stereospecific Kumada Coupling Reactions of Ethers.

Authors:  David D Dawson; Victoria F Oswald; Andy S Borovik; Elizabeth R Jarvo
Journal:  Chemistry       Date:  2020-02-21       Impact factor: 5.236

7.  Ni(I)-Catalyzed β,δ-Vinylarylation of γ,δ-Alkenyl α-Cyanocarboxylic Esters via Contraction of Transient Nickellacycles.

Authors:  Roshan K Dhungana; Shekhar Kc; Prakash Basnet; Vivek Aryal; Lucas J Chesley; Ramesh Giri
Journal:  ACS Catal       Date:  2019-10-29       Impact factor: 13.700

8.  When Weaker Can Be Tougher: The Role of Oxidation State (I) in P- vs N-Ligand-Derived Ni-Catalyzed Trifluoromethylthiolation of Aryl Halides.

Authors:  Indrek Kalvet; Qianqian Guo; Graham J Tizzard; Franziska Schoenebeck
Journal:  ACS Catal       Date:  2017-01-31       Impact factor: 13.084

9.  Divergent Reactivity of a Dinuclear (NHC)Nickel(I) Catalyst versus Nickel(0) Enables Chemoselective Trifluoromethylselenolation.

Authors:  Alexander B Dürr; Henry C Fisher; Indrek Kalvet; Khai-Nghi Truong; Franziska Schoenebeck
Journal:  Angew Chem Int Ed Engl       Date:  2017-09-14       Impact factor: 15.336

10.  Halide Abstraction Competes with Oxidative Addition in the Reactions of Aryl Halides with [Ni(PMen Ph(3-n) )4 ].

Authors:  Ignacio Funes-Ardoiz; David J Nelson; Feliu Maseras
Journal:  Chemistry       Date:  2017-11-20       Impact factor: 5.236

  10 in total

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