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ABSTRACT Immobilized penicillin acylase (from E.coli) was used to catalyze 7 phenylacetamido 3 E propenyl cephalosporanic acid hydrolyzation into 7 amino 3 E propenyl cephalosporanic acid. Then, trans APRA was acylated with hydroxyethyl ester of 4 hydroxy D phenylglycine to obtain trans cefprozil.

以7 苯乙酰氨基 3 E 丙烯基 3 头孢菌素 4 羧酸为原料,在青霉素酰化酶作用下,首先酶法水解得到3 E 丙烯基 3 头孢菌素 4 羧酸,过滤固相酶,滤液调pH分离得到反式APRA固体;在青霉素酰化酶作用下,反式APRA再与对羟基苯甘氨酸乙二醇酯缩合,得到反式头孢丙烯;酶法合成所得的产品与进口反式头孢丙烯对照品一致。

Via comprehensive computations, the possibilities of vinylidene and allene intermediates were excluded, and the reaction mechanism was found to contain the following three steps:(1) gold-catalyzed cyclization to give the cyclic intermediate,(2) the cyclic intermediate undergoing a 1,3-H migration to give a more stable intermediate, with the assistance of water-cluster,(3) finially, the 1,2-H or 1,2-silyl migration occuring for generation of the observed product.

通过对各种可能的反应路径的进行计算和比较,排除了亚甲基卡宾和连二烯中间体的可能性,并确定该异构化反应机理包含以下三个步骤:(1)炔丙基吡啶反应在金催化条件下发生分子内的成环得到环状中间体;(2)环状中间体在水分子簇的协助下优先发生1,3-氢迁移反应,异构化得到更为稳定的中间体;(3)最后再进行1,2-氢迁移或是1,2-硅烷基团迁移即得到实验中所观察到的环异构化产物。

It was found that ARA was composed of esterification products of (2-HEA)-ester with pimaric acid, dehydroabietic acid, abietic acid and two isomers of acrylpimaric acid. ARA is a good crosslinking agent which can copolymerize with most vinyl monomers. The properties of solvent-resistance and heat resistance of the copolymer were improved considerably by the use of ARA.

实验结果表明:ARA主要由海松酸、脱氢枞酸、枞酸和丙烯海松酸的二种异构体的丙烯酸-2-羟基乙基酯的酯化产物组成,ARA是一种良好的交联剂,可与大多数乙烯基单体共聚合,其与MMA的共聚物的耐溶剂性和耐热性均得到了较大幅度的提高。

The all cis-structure of the cyclizative product was found. The construction of the enolic hydroxyl structure became easier and excellent.

合成中发现环化产物为全顺式结构,烯醇式结构的建立更为简洁、高效,异丙基在较复杂的结构下实现了一步引入。

Promoted by metal dysprosium, aldehydes and ketones could react smoothly with propargyl bromide to afford the corresponding homopropargylic alcohol s in good to excellent yields, and no allenic alcohols were found.

在金属镝的促进下,醛、酮可与炔丙基溴反应,高选择性高产率地得到相应的高炔丙醇,没有发现连二烯醇的存在。

Two new active esters of acrylic acids monomers, N-p-acryloxybenzoyloxy succini-mide and N-p-methacryloxybenzoyloxy succinimide have been synthesized and polymerized.ABOSu and MBOSu were prepared by coupling of p-acryloxybenzoic acid or p-methacryloxybenzoie acid with N-hydroxy succinimide in the presence of dicyclohexylcarbodimide.

新的丙烯酸活性酯,N-(对甲基丙烯酰氧苯甲酰氧基)丁二酰亚胺及N-丁二酰亚胺单体分别由对甲基丙烯酰氧基苯甲酸、对丙烯酰氧基苯甲酸与N-羟基丁二酰亚胺在环已基羰二亚胺存在下经偶联反应合成。

This paper mainly studies the synthesis of 2-Isopropyl-5-Methyl-2-Hexenal from the optimum reaction conditions of from self aldol condensation of Isovaleraldehy,with NaOH solution as the catalyst of the condensation.

本文以NaOH水溶液为催化剂,探讨了异戊醛Aldol缩合制备可可醛(2异丙基5甲基2己烯醛)的最佳反应条件:反应温度50℃、反应时间9h、催化剂NaOH水溶液的浓度2mol.L1、OH-/异戊醛为1/1,主产物可可醛的产率为92.2%。

A concentration of 2.5 micrograms per millilitre was effective at reducing the acrylamide-induced ROS production, as well as the preventing the fragmentation of DNA, and effects of cytotoxicity, report Cao and co-workers.

曹及其同僚表示,浓度为2.5微克/毫升的姜黄色素就能有效的减少由丙烯酰胺引起的活性氧自由基的产生,从而可以防止DNA的裂解,同时有效阻止细胞毒素。

The relationship between the melt index, the tensile strength and the stress-crack resistance, and that between the end-group structure and thermal stability of copo-lymer of tetrafluoroethylene and hexafluoropropylene have been studied.

研究了四氟乙烯和六氟丙烯共聚物的熔融指数,抗张强度和耐应力开裂之间,以及端基和热稳定性之间的关系。

Single component and multi\|component of iron system colloidal catalyst \Ali\|Bu\-3CH\-2CHCH\-2Cl\ were mixed by different ratios in hydrogenated gasoline medium at 25℃.This paper studied the relationship between the nonaqueous systematic electroconductivity and the concentration of catalyst components.In combination with Tyndall effect,polymerization experimental results,Ali\|Bu\-3 existed in associated state and dissociated into ionpair.The reaction between Ali\|Bu\-3 and Fenaph\-2 was the main reaction which formed colloidal core.Ali\|Bu\-3 reacted on CH\-2CHCH\-2Cl and Ali\|Bu\-2Cl was yielded which joined the formation of active center on the surface of colloidal core.The excessive Ali\|Bu\-3 was dissociated into ionpair which formed double electrode layer,and the double electrode layer kept the colloidal particles relatively stable.

研究了在25℃加氢汽油介质中,铁系胶体催化剂[Fenaph2Ali-Bu3―CH2==CHCH2Cl]单组分、多组分按不同配比混合,非水体系电导率与浓度的关系,结合Tyndall效应,聚合实验结果,得出Ali-Bu3以缔合状态存在并解离成离子对它同环烷酸亚铁的作用是形成胶核的主要反应,与氯丙烯反应生成的氯化异丁基铝,在胶核表面参与形成活性中心由过量Ali-Bu3解离的离子对形成的双电层结构,使胶粒保持相对稳定。

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