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題 名 | 2'-去氧-5-氟脲核苷(抗腫瘤藥物)之合成法研討 |
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作 者 | 姜宏哲; 王佩蓮; | 書刊名 | 師大學報 |
卷 期 | 26 1981.06[民70.06] |
頁 次 | 頁465-480 |
關鍵詞 | 合成法; 抗腫瘤藥物; |
語 文 | 中文(Chinese) |
英文摘要 | The synthetic methods of 2'-deoxy-5-fluorouridine (an antitumor drug) reported in-literature were extensively reviewed and discussed. The most economical synthetic route is the method modifide by Brown(5) 2', 3', 5'-Tri-O-acetyluridine was allowed to react with acetic acid containing fluorine. The reaction mixture was treated with ammonia in methyl alcohol to give 5-fluououridine. which was then deoxygenated to give the 2'-deoxy-5-fluorouridinein the overall yield 71%. |
本系統中英文摘要資訊取自各篇刊載內容。