共查询到19条相似文献,搜索用时 109 毫秒
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1—(取代异恶唑基)—1,2,4—三唑和1—(取代嘧啶基)—1,2,4—… 总被引:1,自引:0,他引:1
合成了15个新的1-(取代恶唑基)-1,2,4-三唑和1(取代嘧啶基)-1,2,4-三唑化合物,经元素分析、IR、HNMR和MS证实基,对其代表化合物进行抑菌及植物生长调节活性的初步观察。 相似文献
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XU Liang-zhong ZHANG Shu-sheng ** GAO Hong-rong JIAO Kui . College of Chemistry Chemical Engineering Ocean University of China Qingdao P. R. China . Colloge of Chemistry Molecule Engineering Qingdao University of Science Technology Qingdao P. R. China 《高等学校化学研究》2003,19(4):437-441
IntroductionAs an important type of fungicides,triazolecompounds are highly efficient,low poisonous andinward absorbents[1— 4] .At present,the studies ontriazole derivatives have mainly been concentratedon the compounds with triazole group as the onlyactive group.The report of triazloe compoundsthat contain both a triazole group and other activegroups in a single molecule has rarely been found.Some pyrimidines have been used as high efficientand low poisonous fungicides[5] in control of pow-d… 相似文献
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将苯基引入到嘧啶环的4位, 设计、 合成了2个系列共24个结构新颖的磺酰脲类衍生物, 并对其生物活性进行了研究. 抑菌实验结果表明, 目标化合物对苹果轮纹病菌和小麦纹枯病菌表现出优异的抑制率, 其中化合物9f对5种病菌的抑制率均超过65%. 进一步研究发现, 化合物9f对苹果轮纹病菌的EC50值为8.63 mg/L, 略高于对照药百菌清(7.33 mg/L); 化合物8k和9k对小麦纹枯病菌的EC50值分别为5.48和6.09 mg/L, 与百菌清(4.26 mg/L)接近. 同时, 盆栽法除草测试结果表明, 在75 g/ha剂量下, 化合物8d和9d对油菜具有较好的芽前除草活性, 分别为86%和73%; 化合物9h对反枝苋的土壤处理抑制活性为100%, 优于对照药氯磺隆(96%). 相似文献
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WANG Mei-yi MU Xiao-li GUO Wan-cheng LI Yong-hong LI Zheng-ming 《高等学校化学研究》2007,23(6):674-678
Sulfonylurea herbicides have been widely used because of their low application rates,good crop selectivities and low mammalian toxicities.However,some sulfonylureas might persist unfavourably in the environment with residual problems.In order to look for ecologically safer and environmentally benign sulfonylureas,and on keeping the pyrimidine ring being monosubstituted,15 novel C5-monosubstituted benzenesulfonylurea compounds were synthesized.The structures of all the compounds synthesized were confirmed by elemental analysis and 1H NMR.Preliminary herbicidal activities of these new sulfonylurea compounds were determined by ALS screening(in vitro)and pot bioassay experiments(in vivo).The herbicidal results show that some novel sulfonylureas are comparable to commercial Foramsulfuron and Monosulfuron. 相似文献
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新型金属卟啉的合成及其仿酶活性研究 总被引:19,自引:0,他引:19
合成并表征了一系列水溶性和非水溶性金属卟啉3a~3e,5a~5f和8a~8f;测试了这些金属卟啉作为超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的模拟物催化歧化O2-和催化分解H2O2等有毒氧自由基的活性及抗脂质过氧化性质.结果表明,含有吡啶溴化盐的水溶性金属卟啉8a~8f的仿酶活性明显大于含有羟基的非水溶性金属卟啉3a~3e和含有酯基的金属卟啉5a~5f. 相似文献
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Design,Synthesis of Novel Thiourea and Pyrimidine Derivatives as Potential Antitumor Agents 下载免费PDF全文
1,3‐Bis‐(arylidene)thiourea derivatives ( 11a‐c ) were prepared by reacting thiourea ( 9 ) with bezaldehyde, p‐chlorobenzaldehyde or p‐anisaldehyde ( 10a‐c ) respectively. Further reaction of ( 11b ) with acetyl acetone, ethyl acetoacetate, malononitrile and acetic anhydride gave tetrahydropyrimidine‐2‐thiones ( 12‐14 ) and 1,3‐diacetyl thiourea ( 15 ). Compound ( 11b ) reacted with chloroacetyl chloride to give the corresponding pyrimidin‐4‐one derivative ( 16 ). Reaction of ( 12‐14 ) with acetic acid in aqueous sodium nitrite yielded the corresponding oxime derivatives ( 17‐19 ). The triazole ( 20 ) was achieved via refluxing of ( 19 ) in dimethylformamide. Reaction of ( 16 ) with mercaptoacetyl chloride gave the sulfanyl‐acetic acid ( 21 ) which afforded the dihydrazinyl ( 22 ) up on treatment with hydrazine hydrate. Newly synthesized compounds ware characterized by elemental analyses and spectral data (IR, 1H‐NMR, 13C‐NMR and mass spectra). The investigated compounds were screened for their cytotoxicity, i.e. compounds 19 , 20 and 22 exhibited highly potential antitumor activity. 相似文献
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一类新型酰基脲化合物的设计,合成及生物活性 总被引:7,自引:0,他引:7
设计并合成了21个新型含呋喃环的双酰基脲化合物,经IR,^1HNMR、MS和元素分析确证其结构,初步生物活性测定结果表明,该类化合物具有几丁质抑制活性。 相似文献
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In an attempt to search for potent fungicide, a series of novel N-aryl-1H-pyrazole-5-carboxylate derivatives was designed and synthesized. Their chemical structures were characterized by 1H NMR spectra and high resolution mass spectrometry(HRMS). The preliminary bioassay results indicated that some target compounds displayed better fungicidal activities against certain fungi at 50 μg/mL or favorable antitumor activities at 5 μg/mLcompared with chlorothalonil and 5-fluorouracil, respectively. The structure-activity relationship demonstrated that the introduction of ester group and amide bond was favorable to the improvement of activities against Physalospora piricola and Phytophthora capsici. 相似文献