Studies of the SelectiveO-Alkylation and Dealkylation of Flavonoids. V. The Synthesis of 5,6-Dihydroxy-3,4′,8-trimethoxyflavone and a Revised Structure for the Flavone fromConyza stricta
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/55/9/55_9_2933/_pdf
Reference9 articles.
1. The Synthesis of 5,2′-Dihydroxy-6,8-dimethoxyflavone and Its Isomers: A Revised Structure of Skullcapflavone I
2. The Constituents of Domestic Chrysosplenium Genus Plants. : A New Glycoside of Chrysosplenium maximowiczii FRANCH. et SAVAT.
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1. 13C NMR spectral assignment of the A-ring of polyoxygenated flavones;Phytochemistry;1998-03
2. Revised structure of a natural flavone from Tephrosia candida;Phytochemistry;1994-11
3. Studies of the selective O-alkylation and dealkylation of flavonoids. 13. An improved method for synthesizing 5,6,7-trihydroxyflavones from 6-hydroxy-5,7-dimethoxyflavones;The Journal of Organic Chemistry;1992-06
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