CRIS
Permanent URI for this communityhttps://investigadores.udd.cl/handle/123456789/1
Browse
4 results
Search Results
Now showing 1 - 4 of 4
- Some of the metrics are blocked by yourconsent settings
Item type:Publication, Specific nucleophile–electrophile interactions in nucleophilic aromatic substitutions(2013) ;Rodrigo Ormazábal-Toledo ;Renato Contreras ;Ricardo A. TapiaScopus© Citations 30 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Changes in the SNAr reaction mechanism brought about by preferential solvation(2015) ;Jazmín Alarcón-Espósito ;Ricardo A. Tapia ;Renato Contreras<p>For model S<sub>N</sub>Ar reactions in mixtures of acetonitrile and water, we found preferential solvation in favor of the aqueous phase.</p>Scopus© Citations 20 2 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Mechanistic pathways of aromatic nucleophilic substitution in conventional solvents and ionic liquids(2014) ;Marcela Gazitúa ;Ricardo A. Tapia ;Renato Contreras<p>Solvation effects on the reaction mechanism for nucleophilic substitution reactions have been kinetically evaluated in conventional solvents and ionic liquids.</p>1Scopus© Citations 44 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Site activation effects promoted by intramolecular hydrogen bond interactions in SNAr reactions(2014) ;Sebastián Gallardo-Fuentes ;Ricardo A. Tapia ;Renato Contreras<p>The nucleophilic aromatic substitution reaction of benzohydrazide derivatives towards 2-chloro-5-nitropyrimidine is used as model system to experimentally and theoretically show that intramolecular hydrogen-bond formation operates as a perturbation that elicits a dual response at the reaction center of the transition state (TS) structure.</p>1Scopus© Citations 13