Mapping Dual‐Base‐Enabled Nickel‐Catalyzed Aryl Amidations: Application in the Synthesis of 4‐Quinolones-Reference-Cited by-同舟云学术

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Mapping Dual‐Base‐Enabled Nickel‐Catalyzed Aryl Amidations: Application in the Synthesis of 4‐Quinolones

Published:2022-02-11 Issue:13 Volume:61 Page:
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew Chem Int Ed

Author:

McGuire Ryan T.¹,Lundrigan Travis¹,MacMillan Joshua W. M.¹,Robertson Katherine N.²,Yadav Arun A.³,Stradiotto Mark¹^ORCID

Affiliation:

1. Department of Chemistry Dalhousie University 6274 Coburg Road, P.O. Box 15000 Halifax Nova Scotia B3H 4R2 Canada

2. Department of Chemistry Saint Mary's University Halifax Nova Scotia B3H 3C3 Canada

3. Paraza Pharma Inc. 2525 Avenue Marie-Curie Montreal Quebec H4S 2E1 Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202200352

Reference71 articles.

1. Mechanisms of Nickel-Catalyzed Cross-Coupling Reactions

2. Copper catalysed Ullmann type chemistry: from mechanistic aspects to modern development

3. The Buchwald–Hartwig Amination After 25 Years

4. The Buchwald–Hartwig Amination After 25 Years

5. Mechanistic Analysis of Metallaphotoredox C–N Coupling: Photocatalysis Initiates and Perpetuates Ni(I)/Ni(III) Coupling Activity

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1. Harnessing aerial oxygen as an oxidant for dehydrogenation of 2, 3-dihydroquinolones: An application to synthesis of 4-quinolone alkaloids;Tetrahedron;2024-09

2. DalPhos on Demand: Facile Ligand Generation Enables New Ligand Discovery and Expedient Catalyst Screening;ACS Catalysis;2024-02-29

3. Leveraging the Redox Promiscuity of Nickel To Catalyze C–N Coupling Reactions;The Journal of Organic Chemistry;2024-01-17

4. The development of cage phosphine ‘DalPhos’ ligands to enable nickel-catalyzed cross-couplings of (hetero)aryl electrophiles;Chemical Science;2024

5. Ligand-Enabled Nickel Catalysis for the O-Arylation of Alcohols and Phenols with (Hetero)aryl Chlorides Using a Soluble Organic Base;ACS Catalysis;2023-12-26

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