A Practical Synthesis of L-Ribose
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概要
- 論文の詳細を見る
L-Ribose was synthesized by a simple four-step method with overall yield of 76.3% from a protected L-arabinose derivative, which is a compatible intermediate for the synthesis of L-deoxyribose. The key step of this strategy is the Swern oxidation and subsequent stereoselective reduction accompanied by inversion of the 2-hydroxy group of protected L-arabinose.
- 公益社団法人日本薬学会の論文
- 2002-06-01
著者
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Akagi M
Osaka University Of Pharmaceutical Sciences
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Akagi Masao
Osaka University Of Pharmaceutical Sciences
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Urata Hidehito
Osaka University of Pharmaceutical Sciences
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OMAE Daichi
Osaka University of Pharmaceutical Sciences
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TAMURA Yoshinori
Osaka University of Pharmaceutical Sciences
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UEDA Tetsujiro
Osaka University of Pharmaceutical Sciences
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KUMASHIRO Tetsuya
Osaka University of Pharmaceutical Sciences
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Urata H
Osaka University Of Pharmaceutical Sciences
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Urata Hidehito
Osaka College Of Pharmacy
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Tamura Y
Osaka University Of Pharmaceutical Sciences
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