An Effective Synthesis of 5,4'-Disubstituted Flavones via a Cesium Enolate Assisted Intramolecular ipso-Substitution Reaction
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- Matsugi Masato
- Department of Applied Biological Chemistry, Faculty of Agriculture, Meijo University
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- Takeda Masaki
- Department of Applied Biological Chemistry, Faculty of Agriculture, Meijo University
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- Takahashi Ayano
- Department of Applied Biological Chemistry, Faculty of Agriculture, Meijo University
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- Tazaki Takahide
- Department of Applied Biological Chemistry, Faculty of Agriculture, Meijo University
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- Tamura Hiroto
- Department of Applied Biological Chemistry, Faculty of Agriculture, Meijo University
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- Shioiri Takayuki
- Department of Applied Biological Chemistry, Faculty of Agriculture, Meijo University
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抄録
A variety of 5,4′-disubstituted flavones, which are anticipated to be androgen receptor antagonists to treat diseases mediated by the androgen receptor, were synthesized. It was found that an intramolecular ipso-substitution reaction via cesium enolate using 2-fluoro-6-hydroxyacetophenone and various benzoyl chlorides was effective in the preparation of 5-hydroxy-4′-alkylflavones.
収録刊行物
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- ＣＨＥＭＩＣＡＬ ＆ ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ ＢＵＬＬＥＴＩＮ
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ＣＨＥＭＩＣＡＬ ＆ ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ ＢＵＬＬＥＴＩＮ 58 (8), 1107-1110, 2010
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204172722816
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- NII論文ID
- 130000299825
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- NII書誌ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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- NDL書誌ID
- 10764302
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
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- 使用不可