Artículo
In Silico Study on Chemical Properties and Reactivity of Enal Derivatives
Fecha de publicación:
10/2015
Editorial:
Wiley VCH Verlag
Revista:
European Journal of Organic Chemistry
ISSN:
1434-193X
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
The chemical properties and reactivity of enals were explored by means of quantum chemical methods of calculation. The substituent effects were examined by analyzing the formation of oxonium and carbenium intermediates via protonation reactions as models for activation of enals. Considering the nucleophilic addition of organometallic reagents to enals as an important synthetic step, formation and reactivity of the anionic derived species were modeled computationally for the bis-silylated enals and their subsequent reaction with model electrophiles, in order to gain insight into the regio- and stereoselectivity previously observed in electrophilic additions. Silylated enals exhibited interesting features based on the electronic and steric properties of silyl substituents. The present model computations could assist in the development of new synthetic applications for this class of compounds as they find wider synthetic application.
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Articulos(INFIQC)
Articulos de INST.DE INVESTIGACIONES EN FISICO- QUIMICA DE CORDOBA
Articulos de INST.DE INVESTIGACIONES EN FISICO- QUIMICA DE CORDOBA
Citación
Borosky, Gabriela Leonor; Laali, Kenneth K.; In Silico Study on Chemical Properties and Reactivity of Enal Derivatives; Wiley VCH Verlag; European Journal of Organic Chemistry; 2015; 30; 10-2015; 6615-6623
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