STEREOSPECIFIC SYNTHESIS OF NOVEL 1,3-THIAZOLIDIN-2-YL ANALOGUES OF PSEUDOURIDINE
スポンサーリンク
概要
- 論文の詳細を見る
The stereospecific synthesis is described of the first member of a new class of C-nucleoside analogues in which the sugar ring is replaced with a 1,3-thiazolidine ring. The 1,3-thiazolidin-2-yl analogues (1) and (2) of pseudouridine were prepared stereospecifically via condensation of L or D-cysteine with a formylated nucleobase.
- 社団法人日本薬学会の論文
- 1995-09-15
著者
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別所 清
Faculty Of Pharmaceutical Sciences Kyoto University
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多賀 徹
Faculty of Pharmaceutical Sciences, Kyoto University
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三輪 嘉尚
Faculty of Pharmaceutical Sciences, Kyoto University
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柳田 玲子
Faculty of Pharmaceutical Sciences, Kyoto University
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柳田 玲子
京都大学薬学部
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柳田 玲子
Faculty Of Pharmaceutical Sciences Setsunan University
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稲葉 敦宏
Faculty of Pharmaceutical Sciences, Kyoto University
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稲見 浩輔
Faculty of Pharmaceutical Sciences, Kyoto University
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木本 有一
Faculty of Pharmaceutical Sciences, Kyoto University
-
多賀 徹
Faculty Of Pharmaceutical Sciences Kyoto University
-
三輪 嘉尚
Faculty Of Pharmaceutical Sciences Kyoto University
-
木本 有一
Faculty Of Pharmaceutical Sciences Kyoto University
-
稲葉 敦宏
Faculty Of Pharmaceutical Sciences Kyoto University
-
稲見 浩輔
Faculty Of Pharmaceutical Sciences Kyoto University
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