摘要
前文指出,各种1,4-二取代的酰氨基硫脲可在碱性物质催化下脱水环化形成1,2,4-三唑啉-5-硫酮类杂环化合物,然而连接2,2,6,6-四甲基哌啶-1-氧自由基的酰氨基硫脲类化合物能否在相同条件下环化脱水形成类似结构的杂环化合物,迄今未见文献报道。各种3,4-二取代的1,2,4-三唑啉-5-硫酮杂环化合物具有广泛的生物活性,如抗菌,杀虫等,而2,2,6,6-四甲基哌啶-1-
In this paper the synthesis of eight new 3-aryl-4-(4'-2,2,6,6-tetramethyl-pipe-ridine-1-oxyl)-1,2,4-triazoline-5-thiones and the characterization of their structure werereported.Preliminary pharmacodynamic experiments of these compounds showed that mostof them possess inhibiting effect on Bacillus subitilis,Escherichia,Proteus vuigaris and Sta-phylococcus aurreus.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
1991年第2期159-162,共4页
Chinese Journal of Organic Chemistry
关键词
三唑啉硫酮
杂环化合物
三氮唑类
spin label,piperidine nitroxide,1,2,4-triazoline-5-thione
