Diels-Alder adducts from flavonoid |
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| Authors: | Marie-France Laroche Arnaud Marchand Georges Massiot |
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| Institution: | a Centre de Recherche en Oncologie Expérimentale, Division Chimie Médicinale, Pierre Fabre Médicament, ISTMT 3 rue des Satellites BP94244, 31432 Toulouse Cedex 4, France
b Centre de Recherche des Sustances Naturelles, UMS 2597 CNRS/Pierre Fabre, ISTMT 3 rue des Satellites BP94244, 31432 Toulouse Cedex 4, France |
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| Abstract: | A quinoflavonoid was synthesized from commercially available products over three steps. The quinoflavonoid turned out to be an excellent dienophile in Diels-Alder reaction. Reactions were easily performed in dichloromethane, and after evaporation of the solvent, expected products were obtained in good yields. |
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| Keywords: | Diels-Alder reaction Quinoflavonoid |
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