Kinetic solvent isotope effects and activation parameters for the intramolecular addition–elimination between amino and amide groups in 1-amino-8-trifluoroacetylnaphthalene under acidic conditions-Reference-Cited by-同舟云学术

Kinetic solvent isotope effects and activation parameters for the intramolecular addition–elimination between amino and amide groups in 1-amino-8-trifluoroacetylnaphthalene under acidic conditions

Published:1994 Issue:7 Volume: Page:1435-1438
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Baynham Andrew S.,Hibbert Frank

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1994/P2/P29940001435

Reference8 articles.

1. Cyclic imine formation by intramolecular nucleophilic addition and elimination between an amino group and amide carbonyl; rate–pH profile for the reaction of 1-amino-8-trifluoroacetylaminonaphthalene to 2-trifluoromethylperimidine

2. General acid catalysis and kinetic isotope effects for intramolecular, addition–elimination between amino and amide groups in 1-amino-8-trifluoroacetylaminonaphthalene; observation of a biphasic Brønsted plot

3. Intermediates in nucleophilic aromatic substitution. XIV. Spiro Meisenheimer complexes derived from N,N-dimethylethylenediamine. Kinetics in aqueous dimethyl sulfoxide

4. Enforced general acid-base catalysis of complex reactions and its limitations

5. P. M. Laughton and R. E.Robertson in Solute–Solvent Interaction, eds. J. F. Coetzee and C. D. Ritchie, Dekker, New York, 1969, ch. 7, p. 399.

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