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Authordc.contributor.authorMeneses, L. 
Authordc.contributor.authorAraya, A. es_CL
Authordc.contributor.authorPilaquinga, F. es_CL
Authordc.contributor.authorFuentealba Rosas, Patricio es_CL
Admission datedc.date.accessioned2010-01-28T13:45:49Z
Available datedc.date.available2010-01-28T13:45:49Z
Publication datedc.date.issued2008-07-20
Cita de ítemdc.identifier.citationChemical Physics Letters, Volume 460, Issues 1-3, Pages 27-30, 2008en_US
Identifierdc.identifier.issn0009-2614
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/118997
Abstractdc.description.abstractThe Baeyer–Villiger oxidation of some aldehydes and ketones has been revised by using the electrophilicity as a descriptor of reactivity. The global electrophilicity index evaluated at the ground state of a series of aromatic aldehydes and ketones shows a linear relationship with the rp Hammett substituent constants. The theoretical scale correctly accounts for the electrophilic activation/deactivation effects promoted by electron withdrawing and electron releasing substituents in these moleculesen_US
Patrocinadordc.description.sponsorshipWork supported by DGA-PUCE Grant D29101 and FONDECYT Grant 1080184.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevier B.Ven_US
Títulodc.titleRelationship between the electrophilicity and σp Hammett constant in Baeyer–Villiger reactionsen_US
Document typedc.typeArtículo de revista


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