ProPhos: A Ligand for Promoting Nickel-Catalyzed Suzuki-Miyaura Coupling Inspired by Mechanistic Insights into Transmetalation
Author:
Affiliation:
1. Department of Chemistry, New York University, 100 Washington Square East, New York, New York 10003, United States
2. Department of Chemistry, CUNY − Hunter College, 695 Park Ave, New York, New York 10065, United States
Funder
Air Force Office of Scientific Research
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.4c00370
Reference42 articles.
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3. Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited
4. Aryl Mesylates in Metal Catalyzed Homocoupling and Cross-Coupling Reactions. 2. Suzuki-Type Nickel-Catalyzed Cross-Coupling of Aryl Arenesulfonates and Aryl Mesylates with Arylboronic Acids
5. Synthesis of Biaryls via a Nickel(0)-Catalyzed Cross-Coupling Reaction of Chloroarenes with Arylboronic Acids
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2. Deactivation Modes in Nickel-Mediated Suzuki–Miyaura Cross-Coupling Reactions Using an NHC-Pyridonate Ligand;Organometallics;2024-08-10
3. Suzuki-Miyaura Cross-Coupling using convenient and accessible Nickelocene/Phosphine precatalyst;Journal of Catalysis;2024-08
4. Application of Primary Phosphine Oxides in Domino‐Phospha‐Aldol Reactions of Diketones;Advanced Synthesis & Catalysis;2024-07-23
5. Asymmetric 2,3-Addition of Sulfinylamines with Arylboronic Acids Enabled by Nickel Catalysis;Journal of the American Chemical Society;2024-06-24
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