SYNTHESIS OF 1,4-DIKETONES BY MICHAEL ADDITION OF O-AROYLMANDELO-NITRILES INVOLVING REARRANGEMENT OF AROYL GROUP AND DECYANATION
スポンサーリンク
概要
- 論文の詳細を見る
The anions derived form O-aroylmendelonitriles 1 reacted with Michael addition acceptors such as acrylonitrile (7) and methyl acrylate (10) to give the corresponding 1,4-diketones 12,13,and 15 in moderate to good yields. Under acidic conditions, the 1,4-diketones 12,13,and 15 were converted into the furans 17,18 and 19 in good yields.
- 公益社団法人日本薬学会の論文
- 1996-02-15
著者
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Matsuoka Yoshiyuki
School Of Pharmaceutical Sciences University Of Shizuoka
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NUMATA Atsushi
Graduate School of Pharmaceutical Sciences, Tohoku University
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MIYASHITA Akira
School of Pharmaceutical Sciences, University of Shizuoka
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HIGASHINO Takeo
School of Pharmaceutical Sciences, University of Shizuoka
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NUMATA Atsushi
School of Pharmaceutical Sciences, University of Shizuoka
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Numata A
Graduate School Of Pharmaceutical Sciences Tohoku University
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Numata A
Osaka University Of Pharmaceutical Sciences
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Miyashita A
School Of Pharmaceutical Sciences University Of Shizuoka
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Miyashita A
Department Of Applied Chemistry Faculty Of Engineering Saitama University
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Miyashita Akira
Department Of Applied Physics School Of Engineering Nagoya University
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Miyashita Akira
School Of Pharmaceutical Sciences University Of Shizuoka
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Higashino Tt
School Of Pharmaceutical Sciences University Of Shizuoka
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Numata Atsushi
Osaka Univ. Pharmaceutical Sci. Osaka Jpn
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