Phosphinylation of Non‐activated Aryl Fluorides through Nucleophilic Aromatic Substitution at the Boundary of Concerted and Stepwise Mechanisms
Author:
Affiliation:
1. Department of Chemistry Faculty of Science Hokkaido University Sapporo 060-0810 Japan
2. Institute for Chemical Reaction Design and Discovery (WPI-ICReDD) Hokkaido University Kita 21, Nishi 10, Kita-ku Sapporo 001-0021 Japan
Funder
Japan Society for the Promotion of Science
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202013544
Reference81 articles.
1. Aromatic Nucleophilic Substitution Reactions.
2. Rate and equilibrium studies in Jackson-Meisenheimer complexes
3. Fluoride ion as a nucleophile and a leaving group in aromatic nucleophilic substitution reactions
4. For selected reviews on CSNAr reactions see:
5. Facile C–F Bond Formation through a Concerted Nucleophilic Aromatic Substitution Mediated by the PhenoFluor Reagent
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