Electrophilic catalysis in nitro-activated aromtic nucleophilic substitution of fluorine by Piperidine in Benzene.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. The ortho:para Ratio in the Activation of the Nucleophilic Aromatic Substitution by the Nitro Group
2. Effects of o-Methyl and o-Bromine on Rates of Nucleophilic Displacement at Aromatic Carbon. Evidence for the Operation of London Forces1
3. The “Element Effect” as a Criterion of Mechanism in Activated Aromatic Nucleophilic Substitution Reactions1,2
4. Chemismus der Reaktivfarbstoffe
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1. Characterization of solvent mixtures: preferential solvation of chemical probes in binary solvent mixtures of polar hydrogen-bond acceptor solvents with polychlorinated co-solvents;Journal of Physical Organic Chemistry;1999-09
2. Solvent effects on aromatic nucleophilic substitution reactions. Part 9. Special kinetic synergistic behavior in binary solvent mixtures;Journal of Physical Organic Chemistry;1999-06
3. Characterization of solvent mixtures. Part 8 — preferential solvation of chemical probes in binary solvent systems of a polar aprotic hydrogen-bond acceptor solvent with acetonitrile or nitromethane. Solvent effects on aromatic nucleophilic substitution reactions;Journal of Physical Organic Chemistry;1999-03
4. Solvent effects on aromatic nucleophilic substitutions. Part 6. Kinetics of the reaction of 1‐chloro‐2, 4‐dinitrobenzene with piperidine in binary solvent mixtures;Journal of Physical Organic Chemistry;1996-07
5. Reactivity of 2-fluoro-5-nitrothiophene towards sodium thiophenoxide and piperidine. Comparison with other 2-halogeno-5-nitrothiophenes;Journal of Heterocyclic Chemistry;1975-10
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