Studies of the SelectiveO-Alkylation and Dealkylation of Flavonoids. XV. A Convenient Synthesis of 3,5,6-Trihydroxy-7-methoxyflavones and Revised Structures of Two Natural Flavones
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/66/9/66_9_2668/_pdf
Reference14 articles.
1. Studies of the SelectiveO-Alkylation and Dealkylation of Flavonoids. XIV. A Convenient Method for Synthesizing 5,6,7-Trihydroxy-3-methoxyflavones from 6-Hydroxy-3,5,7-trimethoxyflavones
2. Syntheses of 5,7,8- and 5,6,7-trioxygenated 3-alkyl-3',4'-dihydroxyflavones and their inhibitory activities against arachidonate 5-lipoxygenase
3. Inhibition of intestinal .ALPHA.-glucosidases and sugar absorption by flavones.
4. Studies of the selective O-alkylation and dealkylation of flavonoids. XII. A new, convenient method for synthesizing 3,5-dihydroxy-6,7-dimethoxyflavones from 3,5,6,7-tetramethoxyflavones.
5. 3,5-Dihydroxy-7,8-dimethoxyflavones and revised structures for some natural flavones
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2. ChemInform Abstract: Studies of the Selective O-Alkylation and Dealkylation of Flavonoids. Part 15. A Convenient Synthesis of 3,5,6-Trihydroxy-7-methoxyflavones and Revised Structures of Two Natural Flavones.;ChemInform;2010-08-19
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4. 13C NMR spectral assignment of the A-ring of polyoxygenated flavones;Phytochemistry;1998-03
5. Studies of the SelectiveO-Alkylation and Dealkylation of Flavonoids. XVIII. A Convenient Method for Synthesizing 3,5,6,7-Tetrahydroxyflavones;Bulletin of the Chemical Society of Japan;1995-07
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