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ZHANG  Yan WANG  Qin 等 《中国化学》2002,20(2):168-173
Treatment of 4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2,4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2,3-triazole-4-yl)-1,3,4-thiadiazoles with benzaldehyde,acetone and ω-bromoacetophenone was tested and compared.The title compounds Schiff bases,amides,imidazolo [2,1-b]-1,3,4-thiadiazoles and 7H-s-triazolo[3,4-b]-1,3,4-thiadiazines have been confirmed by elemental analyses,^1H NMR,IR and MS spectra.All the compounds have also been screened for their antibacterial activities against B.subtilis,S.aureus and E.coli.  相似文献   

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史达清  路再生 《结构化学》1998,17(6):391-394
标题化合物C23H26O4是水杨醛与5,6-二甲基-1,3-环己二酮在N,N-二甲基甲酰胺中反应而得。结果通过单晶X-射线衍射法确定,其晶体属于单斜晶系,空间群P21/c,a=7.056,b=20.263,c=13.665A,β=93.32,V=1950.7A^3,Mr=366.46,Dc=1.248g/cm^3,Z=4,μ(MOKα)=0.84cm^-1,F(000)=784。晶体结构用直接法解  相似文献   

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周龙虎  张永敏 《结构化学》1998,17(4):273-276
3,4-反-4,5-反-2-氨基-3-氰基-1,3-二乙氧羰基-4,5-二(4-氯苯基)环戊烯  相似文献   

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含有1,2,4三嗪母体环的化合物与核糖连接后,能参与蛋白质分子的合成,改变蛋白质的分子结构,具有抗癌、抗病毒、抗菌及杀虫除草等多种药物活性。作为三嗪类化合物的重要分支,4,6二取代5硫酮1,2,4三嗪3酮由于合成及分离上的困难,目前研究得较少[1][2]。4位为芳香基、6位为叔...  相似文献   

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张万轩  雷策南 《应用化学》1997,14(3):115-116
制备1┐氰基┐2,3,5┐三┐O┐苯甲酰基┐β┐D┐呋喃核糖的简便方法张万轩*雷策南黄锦霞陈家威(湖北大学化学系武汉430062)关键词鸟苷,制备,氰基三苯甲酰基-β-D-呋喃核糖,三甲基氯硅烷1996-08-12收稿,1997-03-05修回1-氰...  相似文献   

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黄君珉  陈茹玉 《结构化学》2001,20(5):354-357
1 INTRODUCTIONOrganophosphorus compounds are ubiquitous in nature and they have broad applications in the fields of agriculture and medicine. During the past two decades, (-ketophosphonates and their derivatives containing sulfur have attracted considerable attention because these compounds are endowed with special physical, chemical and pharmacological properties due to the proximity of the carbonyl and the phosphoryl groups[1~8]. In the study on new pharmacenticals and agrochemicals, th…  相似文献   

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李卫东  渠瑾 《合成化学》1998,6(2):179-183
以香叶基丙酮为起始原料,经五步反应以32%的总收率首次合成了3,7,11,15-四甲基-14-氧代-15-叔丁基二甲基硅氧基-2E,6E,10E-十六碳三烯酸乙酯,它是2-Hydroxyenehpthenol全合成中的酮酯关环前体。  相似文献   

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屠树江  周建峰 《结构化学》2001,20(6):459-461
1 INTRODUCTION Since the discovery of the pharmacological effects of 1,4-dihydropridines(1,4-DHPs) as calcium channel blocks[1], a great deal of work has been directed towards synthesis of the novel 1,4-DHPs acting as calcium antagonists[2, 3]. In fact, it is well-established that slightly modified structures on the DHP exhibit a calcium agents effect[4, 5] ; however, two fused rings have been less well-studied. By refluxing equivalent amounts of dimedone, aromatic aldehyde Meldrum抯 …  相似文献   

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