Reaction of sec-Amides with Metal Hydride. II. Reaction of Acid Chlorides with Sodium Acetanilidoborohydride
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概要
- 論文の詳細を見る
Sodium acetanilidoborohydride prepared from acetanilide and sodium borohydride in α-picoline reduced acid chlorides to alcohols in dichloromethane. On the other hand, this reducing reagent prepared in pyridine did not reduce acid chlorides but reduced the pyridine ring to give acylpiperidines.
- 公益社団法人日本薬学会の論文
- 1976-08-25
著者
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菊川 靖雄
Faculty of Pharmaceutical Sciences, Josai University
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横山 祐作
Faculty of Pharmaceutical Sciences, University of Tokyo
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菊川 靖雄
Faculty Of Pharmaceutical Sciences Josai University
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横山 祐作
Faculty Of Pharmaceutical Sciences University Of Tokyo
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