The reactivity of asymmetric benzo-condensed diazines in the 1,3-dipolar cycloaddition reactions with nitrilimines was investigated. The results demonstrated that, at variance with the symmetric quinoxaline, a certain grade of diastereoselectivity emerged.
Lauria, A., Guarcello, A., Macaluso, G., Dattolo, G., Almerico, A.M. (2009). Reactivity of asymmetric benzo-condensed diazines with nitrilimine dipoles in the 1,3-dipolar cycloaddition reactions. TETRAHEDRON LETTERS, 50(52), 7333-7336 [10.1016/j.tetlet.2009.10.062].
Reactivity of asymmetric benzo-condensed diazines with nitrilimine dipoles in the 1,3-dipolar cycloaddition reactions
LAURIA, Antonino;GUARCELLO, Annalisa;MACALUSO, Gabriella;DATTOLO, Gaetano;ALMERICO, Anna Maria
2009-01-01
Abstract
The reactivity of asymmetric benzo-condensed diazines in the 1,3-dipolar cycloaddition reactions with nitrilimines was investigated. The results demonstrated that, at variance with the symmetric quinoxaline, a certain grade of diastereoselectivity emerged.File in questo prodotto:
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