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Authordc.contributor.authorDomingo, Luis R. 
Authordc.contributor.authorAurell, M. José 
Authordc.contributor.authorPérez, Patricia 
Authordc.contributor.authorContreras Ramos, Renato 
Admission datedc.date.accessioned2018-12-20T14:26:50Z
Available datedc.date.available2018-12-20T14:26:50Z
Publication datedc.date.issued2002
Cita de ítemdc.identifier.citationTetrahedron, Volumen 58, Issue 22, 2018, Pages 4417-4423
Identifierdc.identifier.issn00404020
Identifierdc.identifier.other10.1016/S0040-4020(02)00410-6
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/156025
Abstractdc.description.abstractThe global electrophilicity power, ω, of a series of dienes and dienophiles commonly used in Diels-Alder reactions may be conveniently classified within a unique relative scale. Useful information about the polarity of transition state structures expected for a given reaction may be obtained from the difference in the global electrophilicity power, Δω, of the diene/dienophile interacting pair. Thus the polarity of the process can be related with non-polar (Δω small, pericyclic processes) and polar (Δω big, ionic processes) mechanisms. © 2002 Elsevier Science Ltd. All rights reserved.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceTetrahedron
Keywordsdc.subjectDensity functional theory
Keywordsdc.subjectDiels-Alder reactions
Keywordsdc.subjectElectrophilicity power
Títulodc.titleQuantitative characterization of the global electrophilicity power of common diene/dienophile pairs in Diels-Alder reactions
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile