Studies on nucleosides and nucleotides. V. Selective aroylation of 5'-hydroxyl group of uridine and adenosine.
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概要
- 論文の詳細を見る
When uridine was allowed to react with diethyl azodicarboxylate, triphenylphosphine and either benzoic or <I>p</I>-nitrobenzoic acid at room temperature, 5′-<I>O</I>-aroyluridines were selectively obtained in good yields. Similarly, adenosine gave 5′-<I>O</I>-aroyladenosine. In this case, however, a small amount of <I>N</I><SUP>3</SUP>,5′-cycloadenosine was formed.
- 公益社団法人 日本化学会の論文
著者
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Kimura Junji
Department Of Chemistry And Biological Science College Of Science And Engineering Aoyama Gakuin Univ
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Mitsunobu Oyo
Department Of Chemistry College Of Science And Engineering Aoyama Gakuin University
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Shimokawa Satoru
Department of Chemistry, College of Science and Engineering, Aoyama Gakuin University
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