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Authordc.contributor.authorGonzález Suárez, M. 
Authordc.contributor.authorAizman, Arie es_CL
Authordc.contributor.authorSoto Delgado, Jorge es_CL
Authordc.contributor.authorContreras Ramos, Renato es_CL
Admission datedc.date.accessioned2012-06-08T16:05:23Z
Available datedc.date.available2012-06-08T16:05:23Z
Publication datedc.date.issued2012-01-06
Cita de ítemdc.identifier.citationJOURNAL OF ORGANIC CHEMISTRY Volume: 77 Issue: 1 Pages: 90-95 Published: JAN 6 2012es_CL
Identifierdc.identifier.otherDOI: 10.1021/jo201465g
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119469
Abstractdc.description.abstractThe bond Fukui function is introduced and tested as a new reactivity index capable of predicting the evolution of bond breaking and formation processes during an organic reaction involving pi conjugated systems. As an illustration, we examine many cases where substituted ethylenes and dienes may respond to different reagents to yield cycloaddition, Michael addition, and other reactions at double bonds.es_CL
Patrocinadordc.description.sponsorshipMillennium Nucleus CILIS ICM-P10-003-F Fondecyt 1110062 Department of Physics, UNAB USM 130922es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherAMER CHEMICAL SOCes_CL
Keywordsdc.subjectDIELS-ALDER REACTIONSes_CL
Títulodc.titleBond Fukui Functions As Descriptor of the Electron Density Reorganization in pi Conjugated Systemses_CL
Document typedc.typeArtículo de revista


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