The Effect of the Leaving Group in N-Heterocyclic Carbene-Catalyzed Nucleophilic Aromatic Substitution Reactions
Author:
Affiliation:
1. Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20200210
Reference52 articles.
1. F. A. Corey, R. J. Sundberg,Advanced Organic Chemistry Part A: Structure and Mechanisms Fifth edition; Springer: Berlin, 2007; pp. 389–569.
2. F. Terrier,Modern Nucleophilic Aromatic Substitution; Wiley: New York, 2013; pp. 1–94.
3. Rate and equilibrium studies in Jackson-Meisenheimer complexes
4. The “Element Effect” as a Criterion of Mechanism in Activated Aromatic Nucleophilic Substitution Reactions1,2
5. The Element Effect Revisited: Factors Determining Leaving Group Ability in Activated Nucleophilic Aromatic Substitution Reactions
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