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• W2155212546 abstract "The first total syntheses of ochnaflavone, an asymmetric biflavone consisting of apigenin and luteolin moieties, and the permethyl ether of 2,3,2'',3''-tetrahydroochnaflavone have been achieved. The key steps in the synthesis of ochnaflavone were the formation of a diaryl ether and ring cyclization of an ether-linked dimeric chalcone to assemble the two flavone nuclei. Optimal experimental conditions for the oxidative cyclization to form ochnaflavone were established." @default.
• W2155212546 created "2016-06-24" @default.
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• W2155212546 date "2013-07-08" @default.
• W2155212546 modified "2023-10-13" @default.
• W2155212546 title "Total synthesis of ochnaflavone" @default.
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• W2155212546 doi "https://doi.org/10.3762/bjoc.9.152" @default.
• W2155212546 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3740604" @default.
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