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Authordc.contributor.authorJaramillo, Paula 
Authordc.contributor.authorDomingo, Luis R. es_CL
Authordc.contributor.authorPérez López, Patricia es_CL
Admission datedc.date.accessioned2009-04-09T17:33:04Z
Available datedc.date.available2009-04-09T17:33:04Z
Publication datedc.date.issued2006-03-10
Cita de ítemdc.identifier.citationCHEMICAL PHYSICS LETTERS Volume: 420 Issue: 1-3 Pages: 95-99 Published: MAR 10 2006en
Identifierdc.identifier.issn0009-2614
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/118811
Abstractdc.description.abstractFor an important class of organic reactions in which a fragment of the reactants, the leaving group (LG) or nucleofuge (Z), is detached of the substrate bearing the bonding electron pair, the global electrophilicity index of the CH(3)LG system is proposed as a reliable descriptor of the intrinsic nucleofugality of the LG. The model is illustrated by ranking within a unique relative scale, the LG ability of 28 functional groups commonly involved in substitution and elimination reactions in organic chemistry.en
Lenguagedc.language.isoenen
Publisherdc.publisherELSEVIERen
Keywordsdc.subjectCARBON DOUBLE-BONDSen
Títulodc.titleTowards an intrinsic nucleofugality scale: The leaving group (LG) ability in CH(3)LG model systemen
Document typedc.typeArtículo de revista


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