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N′-叔丁基-N-取代菊酰脲类化合物的合成及其生物活性 被引量:1
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作者 薛思佳 柯少勇 段李平 《应用化学》 CAS CSCD 北大核心 2004年第3期319-321,共3页
Four N′-tert-butyl-N-substituted chrysanthemoyl urea derivatives have been synthesized through "substructure link way": substituted chrysanthemoyl chlorides were directly reacted with tert-butyl urea at abo... Four N′-tert-butyl-N-substituted chrysanthemoyl urea derivatives have been synthesized through "substructure link way": substituted chrysanthemoyl chlorides were directly reacted with tert-butyl urea at about 40 ℃ in the presence of acetonitrile. The structures of the target compounds(2a~2d) were characte- rized by 1H NMR, IR and elemental analysis. The preliminary bioactivity tests showed that compound 2d was active against Cucumber, Chenopodium, Radish and Sorgham. The inhibitory percentage to the root was over 70% and it was also active against the growth of stalks. Compound 2b showed a considerable insecticidal activity. 展开更多
关键词 n′-叔丁基-n-取代菊酰脲 合成 生物活性
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N′-叔丁基-N-取代酰基(硫)脲类化合物的合成及生物活性测定 被引量:11
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作者 薛思佳 柯少勇 段李平 《有机化学》 SCIE CAS CSCD 北大核心 2004年第2期227-230,118,共5页
将叔丁基引入到酰基 (硫 )脲骨架中 ,设计合成了 8个未见文献报道的N′ 叔丁基 N 取代酰基脲及N′ 叔丁氨基羰基 N 取代酰基硫脲类化合物 ,其结构经元素分析、IR和1 HNMR得到确证 .
关键词 n′-n取代 n′--n-取代 合成 生物活性
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