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oai:ojs.www.eurjchem.com:article/756 2013-06-30T03:41:05Z eurjchem:ART driver

Synthesis of new curcumin analogues from Claisen-Schmidt condensation Ziani, Nouara Sid, Assia Demonceau, Albert Willem, Quentin Dassonneville, Benjamin Lamara, Kaddour Curcumin Spectroscopy Benzaldehydes Curcumin analogues Cyclohexanone derivatives Claisen-Schmidt condensation A series of new curcumin analogues were obtained by Claisen-Schmidt condensation of substituted benzaldehydes with cyclohexanone derivatives using the ratio of 1:2 of ketone to aldehyde in dilute ethanolic solution under base catalyzed (NaOH) conditions at room temperature in good yields. The structures of the synthesized compounds were confirmed by data of IR, 1H NMR, and 13C NMR spectra. Atlanta Publishing House LLC 2013-06-30 info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion application/pdf https://www.eurjchem.com/index.php/eurjchem/article/view/756 10.5155/eurjchem.4.2.146-148.756 European Journal of Chemistry; Vol. 4 No. 2 (2013): June 2013; 146-148 2153-2257 2153-2249 eng https://www.eurjchem.com/index.php/eurjchem/article/view/756/PDF