Study of Reactivity in the 1,3-Dipolar Cycloaddition Reactions Leading to New Triazolopyrrolopyrazine Ring Systems

6533b7d1fe1ef96bd125cde2

RESEARCH PRODUCT

Study of Reactivity in the 1,3-Dipolar Cycloaddition Reactions Leading to New Triazolopyrrolopyrazine Ring Systems

Antonino Lauria Annalisa Guarcello Anna Maria Almerico Gaetano Dattolo

subject

Dipole 1 3-Dipolar Cycloaddition Reactions Triazolopyrrolopyrazine Ring Systems Chemistry Organic Chemistry 1 3-Dipolar cycloaddition Structural symmetry Reactivity (chemistry)Ring (chemistry)Photochemistry Settore CHIM/08 - Chimica Farmaceutica Symmetry (physics)Cycloaddition

description

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.

year	journal	country	edition	language
2010-07-28	Synlett

https://doi.org/10.1055/s-0030-1258532

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