1-Phenyl-3-methyl-5-N-benzylideneaminopyrazoles. Substituent effects and protonation sites studied by NMR and ab initio(6-31G*) MO calculations
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1996/P2/P29960002383
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1. Study of the protonation of simple Schiff bases in solvents of various polarity by means of Raman spectroscopy
2. Substituent effects on1H NMR spectra of 4-and 4′-substitutedtras-N-benzylideneanilines in acidic solution
3. Nucleophilic catalysis of hydrolysis of a Schiff base by amines. Intramolecular catalysis of transimination
4. Influence of crystal environment on molecular conformation: p-bromo-N-(p-dimethylaminobenzylidene)aniline
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