In this work we present the Michael addition reaction carried out in micellar media starting from chalcones and acetophenones, to obtain both symmetric and asymmetric Michael adducts. The scope of the asymmetric adducts was expanded using a few chalcones, prepared through micellar-based aldol reaction, and various substituted acetophenones.

Micellar Synthesis of 1,3,5-Triaryl-1,5-Pentanediones

P. Bonino
First
;
F. Cardano;D. Dotta;A. Fin;P. Quagliotto
Last
2025-01-01

Abstract

In this work we present the Michael addition reaction carried out in micellar media starting from chalcones and acetophenones, to obtain both symmetric and asymmetric Michael adducts. The scope of the asymmetric adducts was expanded using a few chalcones, prepared through micellar-based aldol reaction, and various substituted acetophenones.
2025
XLIX “A. CORBELLA” INTERNATIONAL SUMMER SCHOOL ON ORGANIC SYNTHESIS – ISOS 2025
Gargnano (BS), Italy
From 15/06/2025 to 19/06/2025
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Organic Chemistry, Synthesis, Green Chemistry, Micellar Synthesis, Micelles, Surfactant, Chalcone, Pentanediones, Michael Reaction
P. Bonino, F. Cardano, D. Dotta, A. Fin, P. Quagliotto
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/2083191
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