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.accessioned2014-10-27T15:25:49Z
dc.date.available2014-10-27T15:25:49Z
dc.date.issued1984-06-??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.abstractTreatment 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.identifierB98CD3FD-B54B-88C9-8BF0-FA79B13270ACzh_TW
dc.identifier.urihttp://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.publisherOffice of Research and Developmenten_US
dc.relation(29),649-657zh_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.titleSynthesis of 5, 5-Bis(p-methoxy- m -bromophenyl)-2-thiohydantoin Derivativeszh-tw
dc.title.alternative5, 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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