Intramolecular Anion Effect in Polyoxometalate-Based Organocatalysts: Reactivity Enhancement and Chirality Transfer by a Metal Oxide-Organic Cation Interaction - Archive ouverte HAL
Article Dans Une Revue Chemistry - A European Journal Année : 2014

Intramolecular Anion Effect in Polyoxometalate-Based Organocatalysts: Reactivity Enhancement and Chirality Transfer by a Metal Oxide-Organic Cation Interaction

Christian Brazel
  • Fonction : Auteur
Nathalie Dupre
  • Fonction : Auteur
Max Malacria
Emmanuel Lacôte
Serge Thorimbert

Résumé

An (1)-Dawson polyanion bearing a lateral side chain with a 4-aminopyridine end group was synthesized. This organopolyoxometalate catalyzes the addition of indenyl allyl silanes to cinnamoyl fluorides. The polyanionic framework influences the organocatalyst activity and selectivity. A moderate but nonzero chirality transfer from the chiral inorganic framework to the organic substrate was observed.

Domaines

Chimie organique

Dates et versions

hal-01397902 , version 1 (16-11-2016)

Identifiants

Citer

Christian Brazel, Nathalie Dupre, Max Malacria, Bernold Hasenknopf, Emmanuel Lacôte, et al.. Intramolecular Anion Effect in Polyoxometalate-Based Organocatalysts: Reactivity Enhancement and Chirality Transfer by a Metal Oxide-Organic Cation Interaction. Chemistry - A European Journal, 2014, 20 (49), pp.16074-16077. ⟨10.1002/chem.201403989⟩. ⟨hal-01397902⟩
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