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- W2606004983 abstract "Durch Reaktion von o-Benzyloxy-acetophenon mit aromatischen oder heterocyclischen Carbaldehyden im alkalischen Medium werden Chalkone wie (I) (73 10 bis 95% Ausbeute) dargestellt, die mit H2O2 in Gegenwart von NaOH zu Epoxiden wie (II) (67-95%) oxidiert werden; analog werden aus o-Benzyloxy-oz-acetonaphthon mit Benzaldehyd bzw. α-Naphthaldehyd über die Chalkone die entsprechenden Epoxide erhalten." @default.
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- W2606004983 date "1972-04-11" @default.
- W2606004983 modified "2023-10-18" @default.
- W2606004983 title "ChemInform Abstract: FLAVONOIDE 20. MITT. REAKTIONEN SUBSTITUIERTER 2′-BENZYLOXY-CHALKONEPOXIDE" @default.
- W2606004983 doi "https://doi.org/10.1002/chin.197215250" @default.
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