摘要
通过二溴化物与唑酮 1 [R=(CH3) 3C]或α-三唑基苯乙酮 1 (R=Ar)的亲核取代反应 ,合成了新型的环状三唑类化合物 3和 4 ,经元素分析 ,1H NMR,IR,EI-MS和 X射线衍射等方法确证其结构 ,讨论了反应过程 .生物活性测试发现大部分化合物具有很好的杀菌活性 。
The title compounds 3 and 4 were prepared by nucleophilic substitution reaction of compounds 1 with dibromide 2. Their structures were determined by elementary analysis, 1H NMR, IR, EI-MS and X-ray diffraction method. The reaction procedure was also studied in detail. From the screening results of biological activities, most compounds possess good fungicidal activities, especially against Puccinia recondita.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2003年第3期431-435,共5页
Chemical Journal of Chinese Universities
基金
国家自然科学重点基金 (批准号 :2 9832 0 5 0 )资助