Understanding Formation and Roles of Ni<sup>II</sup> Aryl Amido and Ni<sup>III</sup> Aryl Amido Intermediates in Ni-Catalyzed Electrochemical Aryl Amination Reactions-Reference-Cited by-同舟云学术

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Understanding Formation and Roles of Ni^II Aryl Amido and Ni^III Aryl Amido Intermediates in Ni-Catalyzed Electrochemical Aryl Amination Reactions

Published:2023-07-11 Issue:29 Volume:145 Page:16130-16141
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Luo Jian¹^ORCID,Davenport Michael T.²^ORCID,Callister Chad¹,Minteer Shelley D.³^ORCID,Ess Daniel H.²^ORCID,Liu T. Leo¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, Utah State University, Logan, Utah 84322, United States

2. Department of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84604, United States

3. Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States

Funder

Division of Chemistry

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.3c04610

Reference30 articles.

1. Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?

2. Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions

3. The Complementary Competitors: Palladium and Copper in C–N Cross-Coupling Reactions

4. Palladium- and copper-mediated N-aryl bond formation reactions for the synthesis of biological active compounds

5. Electrochemically Enabled, Nickel-Catalyzed Amination

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1. Nickel‐Catalyzed Electrochemical Cross‐Electrophile C(sp²)−C(sp³) Coupling via a Ni^II Aryl Amido Intermediate;Angewandte Chemie International Edition;2024-08-13

2. Nickel‐Catalyzed Electrochemical Cross‐Electrophile C(sp²)−C(sp³) Coupling via a Ni^II Aryl Amido Intermediate;Angewandte Chemie;2024-08-13

3. Photoelectrochemical Ni-catalyzed cross-coupling of aryl bromides with amine at ultra-low potential;Nature Communications;2024-08-12

4. Electro/Ni Dual‐Catalyzed Decarboxylative C(sp³)−C(sp²) Cross‐Coupling Reactions of Carboxylates and Aryl Bromide;Angewandte Chemie International Edition;2024-04-18

5. Electro/Ni Dual‐Catalyzed Decarboxylative C(sp³)−C(sp²) Cross‐Coupling Reactions of Carboxylates and Aryl Bromide;Angewandte Chemie;2024-04-18

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