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Ling SHAO Yah HU Xin ZHOU Zhong JIN Jian Bing LIU Jian Xin FANG 《中国化学快报》2006,17(8):1002-1004
Ferrocenes and their derivatives have been used in material chemistry, electrochemistry and in nonlinear optics. Recently, increasing interests have been focused on their biological activity1. Ferrocifen is a ferrocene derivative of tamoxifen, will be sub… 相似文献
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为了寻找新的含噻唑杂环的先导化合物,利用¨(2-氰基亚胺基-1,3-噻唑烷-3-基)甲基]-2-氨基噻唑与取代苯甲酰氯(或乙酰氯)在吡啶存在下发生缩合反应,合成了19个新型含2-取代-1,3-噻唑烷环的噻唑酰胺类化合物4.经1HNMR和元素分析对目标化合物的结构进行了表征,经MS进一步证实了化合物4s的结构,并通过X射线单晶衍射分析测定了化合物4a的晶体结构.对所合成的目标化合物进行了生物活性测试,部分化合物表现出一定的杀菌和植物生长调节活性. 相似文献
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根据活性基团拼接原理,以对羟基硫代苯甲酰胺和4,4,4-三氟-2-氯乙酰乙酸乙酯为原料,经环化反应制得中间体2-(4'-羟基)苯基-4-三氟甲基-5-噻唑甲酸乙酯(3);3与取代苄基氯或氯乙酸反应合成了5个新型的含醚结构噻唑类化合物(5a~5e),其结构经1H NMR,ESI-MS和元素分析表征。用离体平皿法考察了5a~5e对小麦赤霉病和纹枯病细菌的抑菌活性。结果表明,5a~5e均有一定的抑制活性。其中2-(4'-间氟苄氧基苯基)-4-三氟甲基噻唑-5-甲酸乙酯5c抑菌活性最好,对小麦赤霉病和纹枯病细菌的抑菌活性分别为37.8%和53.3%。 相似文献
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Samuel O. Grim Anthony W. Yankowsky 《Phosphorus, sulfur, and silicon and the related elements》2013,188(2):191-195
Abstract The 31P chemical shifts of eleven (4-ZC6H4)3P compounds show a slight correlation with the Hammet [sgrave]para constant of Z. The unusually large upfield chemical shifts of (2-ZC6H4)3P compounds are attributed to an extreme “gamma” effect caused by the restricted conformations due to the steric influence of the ortho substituents. Chemical shifts are given for about thirty triarylphosphines, and group contributions to phosphine chemical shifts are listed for twenty-one aryl groups. 相似文献
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A. Zablotskaya I. Segal S Germane I. Shestakova I. Domracheva A. Nesterova A. Geronikaki E. Lukevics 《Chemistry of Heterocyclic Compounds》2002,38(7):859-866
Trimethylsilyl ethers of various hydroxyl-containing thiazole derivatives have been synthesized. The psychotropic activity (in vivo) and the cytotoxicity (in vitro on tumor cell lines HT-1080 and MG-22A) of these ethers and of their unsilylated precursors have been studied. It was discovered that the obtained compounds possess a sedative action. A moderate cytotoxic effect was detected for piperidine-containing thiazoles, displayed most strongly in relation to MG-22A cells. 相似文献
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Azomethines containing a thiazole ring have been synthesized and their liquid crystal properties have been investigated. The influence of the central group and substituents in the azomethine component on the type and temperature range of the mesomorphous properties of the compounds synthesized has been elucidated. 相似文献
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《Journal of heterocyclic chemistry》2017,54(6):3395-3402
A series of novel thiazole acrylonitrile derivatives was designed and synthesized utilizing NC‐510 as a precursor. Their structures were characterized by NMR spectrometry, MS, and elemental analysis. The results of bioassay indicated that some of these title compounds exhibited 100% mortality at 50 mg/L against Aphis fabae . In particular, the compound 11c displayed the best activity: Its LC50 value achieved 1.45 mg/L, and its insecticidal potency is comparable with that of NC‐510. 相似文献
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Lu Yu Jiyan Chi Lingling Xiao Jie Li Zhangfei Tang Shuming Tan Pei Li 《Molecules (Basel, Switzerland)》2021,26(10)
A series of novel thiochromanone derivatives containing a sulfonyl hydrazone moiety were designed and synthesized. Their structures were determined by 1H-NMR, 13C-NMR, and HRMS. Bioassay results showed that most of the target compounds revealed moderate to good antibacterial activities against Xanthomonas oryzae pv. oryzae, Xanthomonas oryzae pv. oryzicolaby, and Xanthomonas axonopodis pv. citri. Compound 4i had the best inhibitory activity against Xanthomonas oryzae pv. oryzae, Xanthomonas oryzae pv. oryzicolaby, and Xanthomonas axonopodis pv. citri, with the EC50 values of 8.67, 12.65, and 10.62 μg/mL, which were superior to those of Bismerthiazol and Thiodiazole-copper. Meanwhile, bioassay results showed that all of the target compounds proved to have lower antifungal activities against Sclerotinia sclerotiorum, Fusarium oxysporum, Gibberella zeae, Rhizoctonia solani, Verticillium dahlia, and Botrytis cinerea than those of Carbendazim. 相似文献
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为寻找具有医用或农用生物活性的新颖化合物,以对氯苯胺为起始原料,经由四步反应,制得1-对氯苯基-5-甲基-1,2,3-三唑-4-乙酮缩氨基硫脲(3),随后中间体3与ω-溴代芳基乙酮在无水乙醇中回流或在超声波辐射下反应,得到了一系列新型N-(1-对氯苯基-5-甲基-1,2,3-三唑-4-乙酰基)-N'-(4-芳基-噻唑-2-基)腙类化合物.用1H NMR MS谱和元素分析对所有化合物进行了结构表征.初步生物活性测试表明,化合物4d和4e表现出一定的生物活性. 相似文献
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To further explore the structure-activity relationship(SAR) of amide bridge moeity of anthranilic diamides derivatives, a series of N-pyridylpyrazole derivatives was designed, synthesized and their biological activities were evaluated. The chemical structures of novel target compounds were confirmed by 1H nuclear magnetic resonance (NMR), 13C NMR and elemental analyses(EA). Bioassay results of insecticidal activity demonstrated that the target compound 6h displayed 70% lethality rate against oriental armyworms at 200 mg/L. Moreover, most compounds displayed moderate to excellent antifungicidal activities against Fusarium oxysporum f. sp. cucumerinum, Cercospora arachidicola Hori, Botryosphaeria dothidea, Alternaria solani, Gibberella zeae and Phytophthora capsici at 50 mg/L. In particular, compound 6e showed 61.5% and 92.3% inhibition rate against Cercospora arachidicola Hori and Botryosphaeria dothidea, which was superior to the commercial positive control Chlorothalonil. These results will provide a potential clue for exploring novel high-effective agrochemicals. 相似文献
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A novel series of 3,6-disubstituted coumarin derivatives were synthesized by the reaction of ethyl-2-(3-acetyl-2-oxo-2H-chromen-6-yl)-4-methylthiazole-5-carboxylate with thiosemicarbazide and various phenacyl bromides / 3-(2-bromoacetyl)-2H-chromen-2-ones / 2-(2-bromoacetyl)-3H-benzo[f]chromen-3-one in ethanol having catalytic amount of acetic acid under reflux conditions with good yields. All the synthesized compounds were fully characterized by spectral studies and evaluated for their in vitro antibacterial activity against Pseudomonas aeruginosa, Bacillus subtilis (Gram positive), Escherichia coli, and Azatobacter (Gram negative) bacterial strains. Activity results revealed that the compound 6h against Escherichia coli and compound 6i against Pseudomonas aeruginosa and Escherichia coli have shown maximum zones of inhibition. Remaining compounds showed moderate to good activity against all the tested bacterial strains compared with the standard drug cefotaxime. 相似文献
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Nitin D. Gaikwad Sachin V. Patil Vivek D. Bobade 《Journal of heterocyclic chemistry》2013,50(3):519-527
A series of new 1‐[4‐(2,3,4‐substituted‐phenyl) thiazol‐2‐yl]‐3‐(2,3,4‐substituted‐phenyl)‐1H‐pyrazole‐4‐carbaldehyde ( 4a , 4b , 4c , 4d , 4e , 4f , 4g , 4h , 4i , 4j , 4k , 4l , 4m ), 4‐[4‐(4‐substituted‐phenyl) thiazol‐2‐yl]‐3‐(4‐substituted‐phenyl)‐1‐phenyl‐1H‐pyrazole ( 7a , 7b , 7c , 7d , 7e , 7f , 7g , 7h , 7i ), 4‐[4‐(4‐substituted phenyl)thiazol‐2‐yl]‐1‐phenyl‐1H‐pyrazol‐3‐amine ( 10a , 10b , 10c , 10d , 10e , 10f , 10g ) have been synthesized by using Vilsmeier Haack formylation and Hantzsch reaction in high yield. All the synthesized compounds were tested qualitative (Zone of inhibition) and quantitative antimicrobial activities (MIC). Most of the synthesized compounds showed potent antimicrobial activity against gram positive and gram negative bacteria as well as fungi species. 相似文献