Studies on Acetylenic Compounds. XXXVI. Total Synthesis of Ethyl 3-Amino-3-deoxy-β-DL-arabinofuranoside.
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概要
- 論文の詳細を見る
Ethyl 5-O-(2'-tetrahydropyranyl)-2,3-anhydro-β-DL-lyxofuranoside (VIDL) was predominantly formed by the action of alkali on a chlorohydrin derivative, which was prepared by hypochlorous acid addition of 2'-ethoxy-5-(2'-tetrahydropyranyloxy) methyl-2,5-dihydrofuran (I). Then, ethyl 3-amino-3-deoxy-β-DL-arabinofuranoside (IXDL) was synthesized from VIDL.
- 公益社団法人日本薬学会の論文
- 1963-12-25
著者
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岩井 一成
Central Research Laboratories, Sankyo Co., Ltd.
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浅井 素次
Central Research Laboratories, Sankyo Co., Ltd.
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浅井 素次
Research Laboratories Sankyo Co., Ltd.
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岩井 一成
Research Laboratories, Sankyo Co., Ltd.
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岩重 忠博
Research Laboratories, Sankyo Co., Ltd.
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岩重 忠博
三共中研
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岩井 一成
Central Research Laboratories Sankyo Co. Ltd.
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浅井 素次
Central Research Laboratories Sankyo Co. Ltd.
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