Novel Synthesis of Flavonoids of Scutellaria baicalensis GEORGI
スポンサーリンク
概要
- 論文の詳細を見る
A concise and efficient total synthesis of the flavonoids baicalein, oroxylin A and wogonin was described. Intramolecular oxidative cycli/.ation followed by demethylation of chalcone 1, readily prepared from trimethoxyphenol, afforded, depending upon the controlled conditions, baicalein or oroxylin A in excellent yields. Demethylation of 1 yielded 3, which, by oxidation with I_2/dimethyl sulfoxide (DMSO), was readily converted to oroxylin A and wogonin after column chromatography.
- 社団法人日本薬学会の論文
- 2003-03-01
著者
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Lee A‐r
School Of Pharmacy National Defense Medical Center
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Yang C‐h
School Of Pharmacy National Defense Medical Center
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HUANG Wen-Hsin
School of Pharmacy, National Defense Medical Center
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LEE An-Rong
School of Pharmacy, National Defense Medical Center
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YANG Ching-Huey
School of Pharmacy, National Defense Medical Center
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CHIEN Pei-Yu
School of Pharmacy, National Defense Medical Center
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Chien Pei-yu
School Of Pharmacy National Defense Medical Center
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Lee An-rong
School Of Pharmacy National Defense Medical Center
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Huang Wen-hsin
School Of Pharmacy National Defense Medical Center
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Yang Ching-huey
School Of Pharmacy National Defense Medical Center
関連論文
- Antioxidative and Anti-Inflammatory Activities of Polyhydroxyflavonoids of Scutellaria baicalensis GEORGI
- Novel Synthesis of Flavonoids of Scutellaria baicalensis GEORGI
- Leflunomide Analogues as Potential Antiinflammatory Agents