Studies on Organic Fluorine COmpounds. IL. The Ene Reaction of Trifluoroacetone
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概要
- 論文の詳細を見る
The ene reaction of 1,1,1-trifluoroacetone with various olefinic compounds proceeded in the presence of aluminum chloride at low temperature to give allylmethyl (trifluoromethyl)carbinols. Olefinic compounds with a terminal vinyl group reacted smoothyl, but some olefins with an inner double bond did not react at all. Trifluoroacetone was also found to undergo a Friedel-Crafts type reaction with aromatic compounds.
- 社団法人日本薬学会の論文
- 1986-04-25
著者
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小林 義郎
Tokyo College of Pharmacy
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三木 卓一
Department of Toxicology, Faculty of Pharmaceutical Sciences, Setsunan University
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小林 義郎
東京薬科大学薬学部
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熊懐 稜丸
摂南大・薬
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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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富沢 銀次郎
Tokyo College of Pharmacy
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熊懐 稜丸
摂南大薬
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熊懐 稜丸
Faculty Of Pharmaceutical Sciences Setsunan University
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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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三木 卓一
Department Of Toxicology Faculty Of Pharmaceutical Sciences Setsunan University
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三木 卓一
武田薬品工業株式会社研究開発本部
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冨沢 銀次郎
Tokyo College Of Pharmacy
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Miki Takuichi
Department Of Toxicology Faculty Of Pharmaceutical Sciences Setsunan University
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