The influence of the structural symmetry of the 2-pi double-reactive-sites component in the 1,3-dipolar cycloaddition reactions, involving nitrilimines as dipoles, was investigated. the experimental data showed that the loss of the symmetry leads to the formation of the monocycloadduct in good yields.
Lauria, A., Guarcello, A., Dattolo, G., Almerico, A.M. (2010). Study of Reactivity in the 1,3-Dipolar Cycloaddition Reactions Leading to New Triazolopyrrolopyrazine Ring Systems. SYNLETT, 2010(14), 2067-2070 [10.1055/s-0030-1258532].
Study of Reactivity in the 1,3-Dipolar Cycloaddition Reactions Leading to New Triazolopyrrolopyrazine Ring Systems
LAURIA, Antonino;GUARCELLO, Annalisa;DATTOLO, Gaetano;ALMERICO, Anna Maria
2010-01-01
Abstract
The influence of the structural symmetry of the 2-pi double-reactive-sites component in the 1,3-dipolar cycloaddition reactions, involving nitrilimines as dipoles, was investigated. the experimental data showed that the loss of the symmetry leads to the formation of the monocycloadduct in good yields.
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