Reaction of Trifluoromethyl Ketones. III. : The Aluminum Chloride Assisted Ene Reaction of 1,1,1-Trifluoro-2-hexanone and α, α, α-Trifluoroacetophenone
スポンサーリンク
概要
- 論文の詳細を見る
In the presence of aluminum chloride, 1,1,1-trifluoro-2-hexanone reacts as an enophile with several allyl compounds to give trifluoromethylated homoallyl alcohols. α, α, α-Trifluoroacetophenone reacts similarly with aliphatic allyl compounds, but its reaction with allylbenzene is too slow to be useful for the synthesis of fluorine compounds.
- 社団法人日本薬学会の論文
- 1986-11-25
著者
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永井 隆文
Faculty Of Pharmaceutical Sciences Setsunan University
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三木 卓一
Faculty of Pharmaceutical Sciences, Setsunan University
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熊懐 稜丸
Faculty of Pharmaceutical Sciences, Setsunan University
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Miki T
Takeda Chemical Industries Ltd. Pharmaceutical Research Division
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熊懐 稜丸
Faculty Of Pharmaceutical Sciences Kyushu University:(present Address)tokyo College Of Pharmacy Kash
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永井 隆文
Faculty of Pharmaceutical Sciences, Setsunan University
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