Journal of the Chemical Society. Perkin transactions II p. 181 - 187 (1980)
Update date:2022-08-03
Topics: Ester NMR spectroscopy Thin-layer chromatography (TLC) Nucleophile Electrophile Hydrolysis Mass spectrometry (MS) Kinetics High-performance liquid chromatography (HPLC) Leaving group Reaction Mechanism Solvent Effects Activation Energy Spectroscopic Analysis Rate-determining step pH dependence Reaction quenching
Farrar, Charles R.
Williams, Andrew
The hydrolysis and ethylaminolysis of N-benzoylglycine and N-benzoylsarcosine esters have been studied for a range of leaving hydroxy-functions with pKa from 5.45 to 15.5.Ethylaminolysis of N-benzoylglycinate esters involves kinetic terms in
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