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Authordc.contributor.authorCampodónico, Paola R. 
Authordc.contributor.authorAizman, Arie es_CL
Authordc.contributor.authorContreras Ramos, Renato es_CL
Admission datedc.date.accessioned2008-12-15T16:01:03Z
Available datedc.date.available2008-12-15T16:01:03Z
Publication datedc.date.issued2006-05-10
Cita de ítemdc.identifier.citationCHEMICAL PHYSICS LETTERS Volume: 422 Issue: 4-6 Pages: 340-344 Published: MAY 10 2006en
Identifierdc.identifier.issn0009-2614
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/118767
Abstractdc.description.abstractWe propose and test an empirical nucleofugality index to rank the leaving group ability of a series of molecular fragments present in nucleophilic substitution reactions of carbonyl and thiocarbonyl derivatives. The nucleofugality index is defined as the group electrophilicity of the leaving group embedded in the substrate that undergoes the nucleophilic attack. The reliability and usefulness of this new reactivity index is tested against experimental kinetic data.en
Lenguagedc.language.isoenen
Publisherdc.publisherELSEVIERen
Keywordsdc.subjectSTRUCTURE-REACTIVITY CORRELATIONSen
Títulodc.titleGroup electrophilicity as a model of nucleofugality in nucleophilic substitution reactionsen
Document typedc.typeArtículo de revista


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