The Synthesis of 5,2′-Dihydroxy-6,8-dimethoxyflavone and Its Isomers: A Revised Structure of Skullcapflavone I-Reference-Cited by-同舟云学术

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The Synthesis of 5,2′-Dihydroxy-6,8-dimethoxyflavone and Its Isomers: A Revised Structure of Skullcapflavone I

Published:1979-10 Issue:10 Volume:52 Page:2950-2952
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Horie Tokunaru,Tsukayama Masao,Masumura Mitsuo,Nakayama Mitsuru,Hayashi Shûichi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/52/10/52_10_2950/_pdf

Reference7 articles.

1. Studies on the Constituents in the Water Extracts of Crude Drugs. I. On the Roots of Scutellaria baicalensis GEORGI (Wogon) (1)

2. Synthesis of 5∶6∶7-hydroxyflavones and their derivatives—Part I

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1. Immunosuppressant flavonoids from Scutellaria baicalensis;Biomedicine & Pharmacotherapy;2021-12

2. Compounds derived from acetic acid;Handbook of Hydroxyacetophenones: Preparation and Physical Properties;2005

3. 2 Hydrogen-NMR. Coupling constant. Substance no. 3478ff;Landolt-Börnstein - Group III Condensed Matter;2000

4. 2 Hydrogen-1 NMR. Chemical shift. Substance no. 1844ff;Landolt-Börnstein - Group III Condensed Matter;2000

5. 2 Hydrogen-1 NMR. References;Landolt-Börnstein - Group III Condensed Matter;2000

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