Show simple item record

Authordc.contributor.authorDomingo, Luis R. 
Authordc.contributor.authorPérez, Patricia 
Authordc.contributor.authorContreras Ramos, Renato 
Admission datedc.date.accessioned2018-12-20T14:11:15Z
Available datedc.date.available2018-12-20T14:11:15Z
Publication datedc.date.issued2006
Identifierdc.identifier.issn1434193X
Identifierdc.identifier.other10.1002/ejoc.200500466
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/154524
Abstractdc.description.abstractSmall cycloalkynes possess a π-strain-induced electrophilicity related to the bending of the Csp3-Csp-Csp bond angle. For cyclopentyne and benzyne, the electrophilicity index defined in the context of density functional theory gives a coherent rationale for the reactivity of these cycloalkynes, which may act as electrophiles in polar cycloaddition reactions toward enol ethers. © Wiley-VCH Verlag GmbH & Co. KGaA, 2006.
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.sourceEuropean Journal of Organic Chemistry
Keywordsdc.subjectCycloadditions
Keywordsdc.subjectCycloalkynes
Keywordsdc.subjectDensity functional calculations
Keywordsdc.subjectElectrophilicity
Keywordsdc.subjectStrain
Títulodc.titleπ-strain-induced electrophilicity in small cycloalkynes: A DFT analysis of the polar cycloaddition of cyclopentyne towards enol ethers
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record

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