2'-去氧-5-氟脲核苷(抗腫瘤藥物)之合成法研討
| dc.contributor.author | 姜宏哲 | zh_tw |
| dc.contributor.author | 王佩蓮 | zh_tw |
| dc.date.accessioned | 2014-10-27T15:26:13Z | |
| dc.date.available | 2014-10-27T15:26:13Z | |
| dc.date.issued | 1981-06-?? | zh_TW |
| dc.description.abstract | 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%. | en_US |
| dc.identifier | D2E609D5-F4B8-2C25-A6FD-8C00269ACEA8 | zh_TW |
| dc.identifier.uri | http://rportal.lib.ntnu.edu.tw/handle/20.500.12235/17704 | |
| dc.language | 中文 | zh_TW |
| dc.publisher | 國立臺灣師範大學研究發展處 | zh_tw |
| dc.publisher | Office of Research and Development | en_US |
| dc.relation | (26)，465-480 | zh_TW |
| dc.relation.ispartof | 師大學報 | zh_tw |
| dc.subject.other | 合成法 | zh_tw |
| dc.subject.other | 抗腫瘤藥物 | zh_tw |
| dc.title | 2'-去氧-5-氟脲核苷(抗腫瘤藥物)之合成法研討 | zh-tw |
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