Synthesis of 5, 5-Bis(p-methoxy- m -bromophenyl)-2-thiohydantoin Derivatives
dc.contributor.author | 姜宏哲 | zh_tw |
dc.contributor.author | 王佩蓮 | zh_tw |
dc.date.accessioned | 2014-10-27T15:25:49Z | |
dc.date.available | 2014-10-27T15:25:49Z | |
dc.date.issued | 1984-06-?? | zh_TW |
dc.description.abstract | 取5.5-雙(對甲氧-間溴苯基)-2-硫代乙內醯?(2a),點化甲烷,氫氧化鈉、乙醇、混合加熱,冷?可得到5.5-雙(對甲氧-間溴苯基)-2-甲基硫代乙內醯?(3a),產率81.0%,同樣的方法可合成(b3),(4a-4e)10個衍生物。 | zh_tw |
dc.description.abstract | Treatment of 5,5-bis (p-methoxy-m-bromophenyl)-2-thiohydantoin (2a) with methyl iodide in basic alcohol solution gave 5,5-bis (p-methoxy-m-bromo-phenyl)-2-methythiohydantoin (3a), in 81.0% yield, whose ten new derivatives (3b-3f), (4a-4e) were also prepared in a similar fashion. | en_US |
dc.identifier | B98CD3FD-B54B-88C9-8BF0-FA79B13270AC | zh_TW |
dc.identifier.uri | http://rportal.lib.ntnu.edu.tw/handle/20.500.12235/17595 | |
dc.language | 英文 | 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 | (29),649-657 | zh_TW |
dc.relation.ispartof | 師大學報 | zh_tw |
dc.subject.other | 乙內醯脲 | zh_tw |
dc.subject.other | 合成 | zh_tw |
dc.subject.other | 衍生物 | zh_tw |
dc.subject.other | 硫代 | zh_tw |
dc.subject.other | 雙對甲氧間溴苯基 | zh_tw |
dc.title | Synthesis of 5, 5-Bis(p-methoxy- m -bromophenyl)-2-thiohydantoin Derivatives | zh-tw |
dc.title.alternative | 5, 5﹣雙 (對甲氧﹣間溴苯基)-2-硫代乙內醯脲衍生物之合成 | zh_tw |
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