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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.accessioned2012-06-04T19:42:41Z
Available datedc.date.available2012-06-04T19:42:41Z
Publication datedc.date.issued2011-11-29
Cita de ítemdc.identifier.citationJ. Org. Chem., Vol. 77, p. 90−95, 2012es_CL
Identifierdc.identifier.issn0022-3263
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119447
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 π 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.sponsorshipThis work received financial support from Millennium Nucleus CILIS, ICM-P10-003-F and Fondecyt grant 1110062. M.G.S. acknowledges support from Department of Physics, UNAB. A.A. acknowledges financial support from project USM 130922.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherAmerican Chemical Societyes_CL
Títulodc.titleBond Fukui Functions As Descriptor of the Electron Density Reorganization in π Conjugated Systemses_CL
Document typedc.typeArtículo de revista


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