Studies on Acetylenic Compounds. XXIX. A New Method for Synthesis of DL-Ribose.
スポンサーリンク
概要
- 論文の詳細を見る
DL-Ribose was synthesized stereospecifically by oxidative hydroxylation of 2-ethoxy-5-(tetrahydro-2-pyranyloxy) methyl-2,5-dihydrofuran (VII), which was obtained by hydrogenation of DL-1,1-diethoxy-5-(tetrahydro-2-pyranyloxy)-2-pentyn-4-ol. DL-1,1-diethoxy-5-(tetrahydro-2-pyranyloxy)-2-pentyn-4-ol was prepared by the Grignard reaction of (tetrahydro-2-pyranyloxy)acetaldehyde with propargyl diethyl acetal magnesium bromide.
- 公益社団法人日本薬学会の論文
- 1963-02-25
著者
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富田 和男
Agricultural Chemicals 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
Takamine Research Laboratory, Sankyo Co., Ltd.
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岩重 忠博
Takamine Research Laboratory, Sankyo Co. Ltd.
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岩井 一成
Takamine Laboratory, Sankyo Co., Ltd.
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富田 和男
Takamine Laboratory, Sankyo Co., Ltd.
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平岡 哲夫
Takamine Research Laboratory, Sankyo Co., Ltd.
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井手 純也
Takamine Research Laboratory, Sankyo Co., Ltd.
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井手 純也
Sankyo Research Laboratories, Sankyo Co., Ltd.,
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井手 純也
Sankyo Research Laboratories Sankyo Co. Ltd.
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岩重 忠博
三共中研
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岩重 忠博
Takamine Research Laboratory Sankyo Co. Ltd.
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平岡 哲夫
三共(株)総合研究所
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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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