Total Synthesis of (±)-Plumbazeylanone
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概要
- 論文の詳細を見る
The first total synthesis of plumbazeylanone (1), which is a trimer of naphthoquinone, was carried out successfully utilizing the unsymmetrical methylene-bridged dimer with the naphthoquinone unit and the naphthol unit, 11b as a key intermediate in 11 steps. This synthesis features a regioselective nucleophilic 1,2-addition reaction and dinone-phenol-type rearrangement.
- 公益社団法人日本薬学会の論文
- 1998-10-15
著者
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TAKEYA Tetsuya
Showa College of Pharmaceutical Sciences
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TOBINAGA Seisho
Showa College of Pharmaceutical Sciences
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Takeya T
Showa Pharmaceutical University
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Tobinaga S
Showa Pharmaceutical University
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KAJIYAMA Manabu
Showa College of Pharmaceutical Sciences, Machida
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NAKAMURA Chikara
Showa College of Pharmaceutical Sciences, Machida
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Nakamura C
Showa College Of Pharmaceytical Sciences
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Kajiyama Manabu
Showa College Of Pharmaceytical Sciences
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KAJIYAMA Manabu
Showa College of Pharmaceutical Sciences
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