Direct conversion to 2-phenyl-4-quinolon
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Shingo Sato; Hironobu Kumagai; Shigeru Matsuba; Toshihiro Kumazawa; Jun-Ichi Ono
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Article
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1999
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Journal of Heterocyclic Chemistry
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English
⚖ 201 KB
## Abstract A flavanone, in which a hydroxyl group at the 5‐position was protected with a methyl group, converted to the corresponding 5‐methoxy‐2‐phenyl‐4‐quinolone __via__ flavylium salt under mild conditions. Flavanone‐__O__‐rhamnoglucoside, naringin, was also converted to 5‐methoxy‐2‐phenyl‐4‐q