Accéder au contenu
Merck

Highly enantioselective nitrone cycloadditions with 2-alkenoyl pyridine N-oxides catalyzed by Cu(II)-BOX complexes.

Organic letters (2010-12-24)
Santiago Barroso, Gonzalo Blay, M Carmen Muñoz, José R Pedro
RÉSUMÉ

Enantioselective nitrone cycloadditions with 2-alkenoyl pyridine N-oxides as dipolarophiles have been reported. The reaction is catalyzed by Cu(II)-BOX complexes to give the expected isoxazolidine products with high diastereo- and enantioselectivity.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Pyridine N-oxide, 95%