Effect of Lewis acid bulkiness on the stereoselectivity of Diels-Alder reactions between acyclic dienes and α,β-enals

Diana Yepes, Patricia Pérez, Pablo Jaque, Israel Fernández

Resultado de la investigación: Article

11 Citas (Scopus)

Resumen

The factors controlling the reactivity and endo/exo selectivity of Lewis acid-catalysed Diels-Alder reactions between highly substituted open-chain 1,3-dienes and α,β-enals have been explored computationally by means of density functional theory calculations. In agreement with previous experimental observations, it is found that the B(C6F5)3-catalysed cycloaddition reaction leads almost exclusively to the corresponding exo-cycloadduct, whereas the analogous AlCl3-mediated process is highly endo-selective. The effect of Lewis acid bulkiness on stereoselectivity has been quantitatively analysed by means of a combination of the activation strain model of reactivity and the energy decomposition analysis methods. In contrast to the current view, the exo-selectivity promoted by the bulky B(C6F5)3 catalyst does not result from the steric destabilization of the corresponding endo-transition state but from the interplay between the less destabilizing strain energy and the stronger interaction between the deformed reactants along the entire reaction coordinate. In addition, non-covalent interactions are found to play a crucial role in stabilizing the exo-approach. These results allow us to not only quantitatively understand the effect of the Lewis acids in the process, but also predict new catalysts leading to highly exo-selective Diels-Alder reactions.

Idioma originalEnglish
Páginas (desde-hasta)1390-1399
Número de páginas10
PublicaciónOrganic Chemistry Frontiers
Volumen4
N.º7
DOI
EstadoPublished - 1 jul 2017

Huella dactilar

Stereoselectivity
Lewis Acids
Catalysts
Cycloaddition
Catalyst selectivity
Strain energy
Density functional theory
Chemical activation
Decomposition

ASJC Scopus subject areas

  • Organic Chemistry

Citar esto

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abstract = "The factors controlling the reactivity and endo/exo selectivity of Lewis acid-catalysed Diels-Alder reactions between highly substituted open-chain 1,3-dienes and α,β-enals have been explored computationally by means of density functional theory calculations. In agreement with previous experimental observations, it is found that the B(C6F5)3-catalysed cycloaddition reaction leads almost exclusively to the corresponding exo-cycloadduct, whereas the analogous AlCl3-mediated process is highly endo-selective. The effect of Lewis acid bulkiness on stereoselectivity has been quantitatively analysed by means of a combination of the activation strain model of reactivity and the energy decomposition analysis methods. In contrast to the current view, the exo-selectivity promoted by the bulky B(C6F5)3 catalyst does not result from the steric destabilization of the corresponding endo-transition state but from the interplay between the less destabilizing strain energy and the stronger interaction between the deformed reactants along the entire reaction coordinate. In addition, non-covalent interactions are found to play a crucial role in stabilizing the exo-approach. These results allow us to not only quantitatively understand the effect of the Lewis acids in the process, but also predict new catalysts leading to highly exo-selective Diels-Alder reactions.",
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Effect of Lewis acid bulkiness on the stereoselectivity of Diels-Alder reactions between acyclic dienes and α,β-enals. / Yepes, Diana; Pérez, Patricia; Jaque, Pablo; Fernández, Israel.

En: Organic Chemistry Frontiers, Vol. 4, N.º 7, 01.07.2017, p. 1390-1399.

Resultado de la investigación: Article

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