5-去氢枞基-1,3,4-噻二唑衍生物的合成和除草活性(英文)  

Synthesis and Herbicidal Activity of 5-Dehydroabietyl-1,3,4-thiadiazole Derivatives

作　　者：段文贵[1] 李行任[1] 马献力[1,2] 莫启进[1] 许雪棠[1] 岑波[1] 

机构地区：[1]广西大学化学化工学院,广西南宁530004 [2]桂林医学院药学院,广西桂林541004

出　　处：《林产化学与工业》2011年第1期1-8,共8页Chemistry and Industry of Forest Products

基　　金：广西林产化学品开发与应用重点实验室开放基金项目(GXFC08-04);广西自然科学基金重点项目(2010GXNSFD013013)

摘　　要：为了寻找具有更高生物活性的新颖化合物,设计并合成了具有1,3,4-噻二唑骨架的系列新型去氢枞酸衍生物。在磷酸催化下,通过中间体1-去氢枞酰基-4-取代基氨基硫脲4(a～h)的关环反应,合成得到8个目标产物5-去氢枞基-2-取代氨基-1,3,4-噻二唑5(a～h),并采用IR、UV、EI-MS、1HNMR、13C NMR和元素分析等方法对其进行了分析和表征。初步生物活性测试结果表明:所有这些目标化合物均对油菜(Brassica campestris)表现出良好的抑制作用,对稗草(Echinochloa crusgalli(L.))有一定的抑制活性。In order to search for novel compounds with higher biological activity, a series of new dehydro- abietic acid derivatives bearing 1,3,4-thiadiazole moieties were designed and synthesized. Eight title cornpounds of 5-dehydroabietyl-2-substituted amino-1 ,3,4-thiadiazoles 5 （a-h） were synthesized by the eyclization of 1-dehydroabie- tacyl-4-substituted thiosemicarbazides 4（a-h） under the catalysis of phosphoric acid. All the title compounds were analyzed and characterized by means of IR, UV, EI-MS, ^1H NMR, ^13C NMR, and elemental analysis. The preliminary bioassay showed that all these title compounds exhibited exeellent growth inhibition against rape （Brasslca campestrls） and a certain inhibition against barnyard grass Echinochloa crusgalli （L.）.

关 键 词：去氢枞酸 1 3 4-噻二唑 合成 除草活性 

分 类 号：TQ351[化学工程]