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对文献合成方法进行了改进.以N—Boc氨基酸与自制甲烷磺酸酯反应,制备N—Boc氨基酸丙烯酯,以混合酸酐法实现关键中间体与1-胸腺嘧啶乙酸的缩合,总收率为26.4%,比文献方法提高了12%,成本降低,制备了含丝氨酸残基碱基为胸腺嘧啶的手性肽核酸单体.  相似文献   
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以L-组氨酸为起始原料,设计合成了含组氨酸残基的手性肽核酸单体.以叔丁氧羰基(Boc)保护α-氨基,羧基形成苄酯加以保护,分别以苄氧羰基(Cbz)及2,4-二硝基苯基(Dnp)作为咪唑基的临时和永久保护基,共九步反应,手性肽核酸单体总收率13.3%.  相似文献   
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0 IntroductionThemethodofmineralizingorganictoxicantsinthewastewaterbygenerating·OHradicalshasbecomefocusofchemicaltheoriesandtechnicalresearchesintheenvironmentprotection[1] .Because·OHradicalisastrongoxidizerwithstandardpotentialof2 .80V ,withit,thestable…  相似文献   
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(S)-2-甲氧基环己酮为制备抗菌药Tribactam侧链的关键中间体.本研究工作设计以1,2-环氧环己烷为起始原料,经甲醇取代开环、酯化、缬氨酸手性拆分、皂化、氧化,得到光学纯的(S)-2-甲氧基环己酮;总收率14.32%.  相似文献   
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The characteristic of electrochemical oxidation of aniline on SnO2/Ti electrode is studied. The results indicate that SnO2/Ti electrode dopedF plays a wonderful role in the oxidation of aniline comparing with Pt electrode. The kinetics factors that influence the oxidation rate of aniline on the SnO2/Ti electrode are determined by the dissolving of the film on the electrode. The dissolving of the film consisted of intermediate products on the electrode is the slow step. The effects of aniline concentration, pH in aniline solution and the current density (i) on the rate of aniline oxidation, the complexity of intermediate products and the basic category of the intermediate products consisted of the film are introduced. Foundation item: Supported by the National Natural Science Foundation of PRC(10971023) Biography: Wany Yu-ling (1975-), female, Master, research direction: photochemical catalysis and electochemical catalysis.  相似文献   
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A novel reaction system consisted of a supported TiO2 film electrode, a Ru−Ti oxide film electrode and air (oxygen) electrode is reported. The air (oxygen) electrode can provide H2O2 continuously for homogeneous photochemical oxidation reaction on the spot. In this reactor, degradation reaction of aniline occur from interface of TiO2 film to all solution which is irradiated by ultraviolet ray. The degradation rate of aniline was characterized by measuring the change of chemical oxygen demand (COD) in solution under different conditions. It was found that the degradation rate of aniline in the novel system increased apparently as compared with single heterogeneous photocatalysis and homogeneous photochemistry system. It can be explained in terms of combining acts of heterogeneous photocatalysis and homogeneous photochemistry. Foundation item: Supported by the National Natural Science Foundation of China (10791033) Biography: CAI Nai-cai (1946-), male, Associate professor, Research direction: electrochemical catalysis and photocatalysis.  相似文献   
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以1,2,4-三-O-乙酰基-4-O-苄基-α/β-L艾杜糖醛酸甲酯为起始原料,经溴化、糖苷化、脱乙酰基和选择性乙酰化合成了甲基6-O-乙酰基-3-O-苄基-2-苄氧碳酰氨基-2-脱氧-4-O-(2-O-乙酰基-3-O-苄基-α-L-吡喃艾杜糖醛酸甲酯)-α-D-吡喃葡萄糖(FPS-1306),其中2个中间体为新化合物,结构经1H NMR、13C NMR和MS表征.  相似文献   
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A gas diffusion electrode (air electrode) with a high current efficiency of electro-synthesizing H2O2 using O2 in air was prepared. The several systems with air electrode as cathode of electro-synthesizing H2O2 on the reaction spot for degrading aniline in aqueous—electro-Fenton system, photo-excitation electro-H2O2 system and photo-electro-Fenton system, were developed. The rates of decomposition of H2O2 and mineralization of aniline were experimentally measured respectively under different conditions, and the results indicated there has an excellent parallel relation between decomposition rate of H2O2 and mineralization rate of aniline. Especially, photo-electro-Fenton system, where H2O2 is decomposed the fastest, is the best system of oxidizing and degrading organic toxicants. Compared photo-electro-Fenton system with photo-Fenton system, important role is revealed in the interface of air electrode. In this paper, the mineralization mechanism of aniline in the photo-electro-Fenton system was also discussed. Foundation item: Supported by the National Natural Science Foundation of China (200710026) and Foundation of Environmental Sciences Academy of Jiangsu Province. Biography: Cao xiao-yu (1979-), male, Master candidate, research direction: Electrochemistry  相似文献   
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