Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5385700 | Chemical Physics Letters | 2010 | 4 Pages |
Abstract
In the reaction of a series of benzohydrazide derivatives towards p-nitrophenyl acetate, benzohydrazide derivatives establish intramolecular proton rearrangement leaving the enol form as the proximate nucleophile. This feature explains the low response in the reaction rate coefficients expected from inductive substituent effects.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Paola R. Campodónico, Margarita E. Aliaga, José G. Santos, Enrique A. Castro, Renato Contreras,