Main content area

Organocatalytic asymmetric vinylogous 1,4-addition of α,α-Dicyanoolefins to chalcones under a bio-based reaction media: Discovery of new Michael adducts with antiplasmodial activity

Martelli, Lorena S.R., Vieira, Lucas C.C., Paixão, Márcio W., Zukerman-Schpector, Julio, de Souza, Juliana O., Aguiar, Anna Caroline C., Oliva, Glaucius, Guido, Rafael V.C., Corrêa, Arlene G.
Tetrahedron 2019 v.75 no.25 pp. 3530-3542
Cinchona, aldehydes, alkaloids, antimalarials, antiplasmodial properties, catalysts, catalytic activity, chalcones, chemical reactions, chemical structure, cytotoxicity, diastereoselectivity, ketones, solvents, toluene
The organocatalysed asymmetric vinylogous Michael addition of α,α-dicyanoolefins to α,β-unsaturated aldehydes and ketones have been reported in the last decade, however, chalcones have been poorly explored. Moreover, a considerable part of the publications in this theme still employs undesirable solvents, such as toluene and THF, with concerns related to health and environmental safety. We report herein the use of a bifunctional catalyst derived from a Cinchona alkaloid to perform the enantio- and diastereoselective Michael addition of α,α-dicyanoolefins to chalcones using 2-MeTHF as solvent. The Michael adducts were obtained in moderate to good yields and were evaluated for their antiplasmodial and cytotoxic activity.