dc.creator | Pérez Méndez, Claudio | |
dc.creator | Contreras Ramos, Renato | |
dc.date.accessioned | 2015-07-30T14:36:47Z | |
dc.date.available | 2015-07-30T14:36:47Z | |
dc.date.created | 2015-07-30T14:36:47Z | |
dc.date.issued | 2015 | |
dc.identifier | Tetrahedron Letters 56 (2015) 1767–1770 | |
dc.identifier | doi: 10.1016/j.tetlet.2015.01.199 | |
dc.identifier | https://repositorio.uchile.cl/handle/2250/132240 | |
dc.description.abstract | We present a unified model of electrophilicity and nucleophilicity that considers the electrophile/nucleophile
pair in an interacting regime, thereby avoiding the arbitrariness of defining them as the opposite
ends of a unique reactivity scale. The model is validated against rate coefficients for the cycloaddition of
azomethine ylides towards substituted acetylenes and Michael addition of a series of 1-(X-substituted
phenyl)-2-propyn-1-ones towards hydrazine. | |
dc.language | en | |
dc.publisher | Elsevier | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.rights | Atribución-NoComercial-SinDerivadas 3.0 Chile | |
dc.subject | Nucleophilicity | |
dc.subject | Electrophilicity | |
dc.subject | Cycloaddition | |
dc.subject | Michael addition | |
dc.title | Quantitative characterization of the global philicity patterns of common diene/dienophile pairs in cycloaddition reactions II: the interacting pair model | |
dc.type | Artículo de revista | |