A New Synthetic Method of 3-Formylcephalosporins
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概要
- 論文の詳細を見る
Cephalosporin 3'-bromolactones (3) were prepared in good yields via silyl ethers (2) starting from readily available cephalosporin lactones (1). Treatment of 3 with dimethyl sulfoxide yielded 3-formylcephalosporins (4), a useful intermediate for the chemical modification at the C_3-position of cephalosporins.
- 公益社団法人日本薬学会の論文
- 1980-04-25
著者
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松尾 泰介
Central Research Division, Takeda Chemical Industries, Ltd.
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川野 泰彦
Central Research Division, Takeda Chemical Industries, Ltd.
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川野 泰彦
Pharmaceutical Research Division Pharmaceutical Research Laboratories Iii Takeda Chemical Industries
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川野 泰彦
Central Research Division Takeda Chemical Industries Ltd.
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菅原 徹
Molecular Chemistry Laboratory, Takeda Chemical Industries Ltd.,
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桑田 胖
Central Research Division, Takeda Chemical Industries, Ltd.
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菅原 徹
Molecular Chemistry Laboratory Takeda Chemical Industries Ltd.
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菅原 徹
Central Research Division, Takeda Chemical Industries, Ltd.
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桝屋 浩大
Central Research Division, Takeda Chemical Industries, Ltd
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桑田 胖
Central Research Division Takeda Chemical Industries Ltd.
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桝屋 浩大
Central Research Division Takeda Chemical Ind. Ltd.
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松尾 泰介
Central Research Division Takeda Chemical Industries Ltd.
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