三羟基的

Three ways leads to the synthesis of fenclorin, one way discussed here has 3 steps. Stepl :benzonitrile using as raw material goes though dry hydrogen chloride and becomes a-imino phenylmethyl ether after meet carbinol.

解草啶的合成主要有三条路线，本文选取合成路线是以苯甲腈为原料，经三步反应而成：1、苯甲腈在干燥的氯化氢通入，与甲醇形成亚氨基苯甲醚，通入氨气后置换甲氧基得到苯基脒盐酸盐(收率76.18%)。2、苯基脒盐酸盐在碱性条件下与丙二酸二乙酯环合而得嘧啶醇(收率84.39%)。3、嘧啶醇在三氯氧磷中羟基被氯化得到产品解草啶(收率87.29%)。

Cephalotaxine ester of 2-oxo-6-methylheptanoic acid was treated with lithium diisopropylamide and Me O-(1-methoxyisopropyl)glycolate to give a mixture of homoisoharringtonine and its stereoisomers with 56% yield. The four stereoisomers separated by TLC showed identical mass spectra and almost superimposed IR but with different 1H NMR spectra. The configuration of the 2'-C and 3'-C of the four isomers were postulated based upon their 1H NMR spectra as compared with the 1H NMR spectra of isoharringtonine and its stereoisomers.

2-氧代-6-甲基庚酰基三尖杉碱(3)与0-(1-甲氧基异丙基)羟基乙酸甲酯(4)在强碱性试剂二异丙胺锂存在下，起亲核加成反应，反应中间体5在室温用酸性丙酮水解，得到一种新的三尖杉酯类生物碱一一高异三尖杉酯碱(6c)及其立体异构体(6a、6b、6d)的混合物，产率56%、通过制备薄层层析分得这四个立体异构体，它们的1H NMR和异三尖杉酯碱及其立体异构体的1H NMR类似，推定了它们的绝对构型。

In the rhombohedron, each top site is occupied by a pair of ligand-unsupported Ag atoms which are surrounded by six phenol groups in an ethane-like structure. The phenol groups at another ends of the ligands bridge the rhombohedrons into novel non-interpenetrating three-dimensional network.

在每个棱柱体内，每个顶点由无桥连配体支持的、周围的六个酚羟基以一种不寻常的、类似于乙烷分子结构的扭曲方式排列的一对 Ag 原子占据，配体另一端酚羟基将棱面体连接成新颖的非穿插的具有棱形通道(沿 a 和 b 轴方向)的三维网络结构。

The results indicated that the Fe3+ ion of Fe-AO-PAN was coordinated with three amino nitrogen atoms and three hydroxyl oxygen atoms of three amidoxime units on the surface of AO-PAN by covalent bond, and the coordination number was six.

结果表明， Fe-AO-PAN中的Fe3+能够与AO-PAN表面三个偕胺肟链节单元的三个氨基氮原子和三个羟基氧原子进行配位反应，配位数为6。

Those biodegradable materials finally form into CO2 and H2O via culture of tricarboxylic acid cycle, which can be excreted from lung, kidney, and skin. Hydroxyacetic acid is a metabolic product of amino acids. Therefore, velocity of bioldegradable materials can be controlled in vivo. The recent contraception focuses on discover a sustained release system of biodegradable materials.

生物可降解材料包括聚乳酸、聚ε-己内酯、乳酸-羟基乙酸共聚物等，这些材料有很好的生物相容性，植入体内后可经生物降解成乳酸单体，经三羧酸循环后最终成为CO2和H2O，经肺、肾、皮肤排泄，羟基乙酸也是机体氨基酸代谢产物，而且生物可将解材料在体内降解速度是可控的，用生物降解聚合物作为药物载体的缓释避孕系统是目前材料学以及避孕节育研究的一大重点。

Three part of research works had been carried out in the dissertation. The first part: a kind of multidentate amine modified silica gel was synthesized through the following steps:(1) introduce the amino groups onto the surface of silica-gel by the treatment of surface silanol groups withγ-aminopropyl trimethoxy silane;(2) michael addition of excess trihydroxymethyl propyl triacrylate to amino groups on the silica gel surface;(3) amidation of the unreacted double bonds of TMPTA on the surface of TMPTA modified silica gel with diethylenetriamine;(4) the multidentate amine modified silica gel was finally obtained by the reaction of amino groups on the surface of DETA modified silica gel with double bond of butyl acrylate.

本论文进行了三部分研究工作，第一部分：通过多步反应对硅胶进行改性合成了一种多齿胺改性硅胶配体，合成过程如下：1通过γ-氨丙基三甲氧基硅烷与硅胶表面的硅羟基反应，使硅胶表面带有氨基；2利用硅胶表面氨基与过量的三羟甲基丙烷三丙烯酸酯发生Michael加成反应；3利用二乙烯三胺与TMPTA改性硅胶表面未反应的双键发生反应使硅胶表面氨基化；4最后用丙烯酸正丁酯与DETA改性硅胶表面氨基充分反应成功合多齿胺改性硅胶配体。

Novel rod like phenylene thiophene based polyhydroxy amphiphiles, derivatives of gallic acid combining three hydrophilic 2,3-dihydroxypropyloxy groups and one alkyl chain via central aromatic linking units, have been synthesized by using Ni, Pd(0) catalyzed coupling reaction as key steps.

以Ni， Pd (0)催化的C-C偶合反应为关键步骤合成了基于苯联噻吩的棒状型多羟基两亲性分子，它们是以棒状芳香核为中心部分，一端带三重亲水的2，3-二羟基链，另一端为带一条烷基链的没食子酸衍生物。

All of the tripodal schiff base ligands and their complexes were characterized.

以三乙醇胺、巯基苯胺、巯基乙胺为初始原料，设计合成了六个三脚架结构的化合物，其合成路线如下：三乙醇胺与氯化亚砜反应得到三(2-氯乙基)胺(1)，然后与巯基苯胺或巯基乙胺在碱性条件下反应生成三脚架结构的三{[2-(2-氨基苯基)硫代]乙基}胺(2)或三{[2-(2-氨基乙基)硫代]乙基}胺(3)，然后再与水杨醛、2-甲酰基-8-羟基喹啉(8)、2-甲酰基-8-苄氧基喹啉(7)反应得到六种新型的含硫西佛碱化合

In chapter 3, general reaction of a-hydroxy epoxides were introduced. We have developed a newly gold-catalyzed ring opening reaction ofα-hydroxy epoxides containing carbon cycle. We have disclosed the rule of ring opening reaction. And the plausible mechanism was proposed.

第三章：首先介绍了α-羟基环氧化合物的反应，其次介绍了一个新的金催化的含碳环骨架的α-羟基环氧化合物开环反应，总结了反应规律，提出了可能的反应机理。

This research utilized the method of organic synthesis, researching different amounts and positions of hydroxy-substituted benzoic acid and serotonin into amide reaction, so as to produce a series of polyhydroxy substituted N-benzoylserotonin derivatives (compound 1-10). Accordingly, this study conducts the following four tests. I. The activity of antioxidant and the experiment of ability to scavenge DPPH free radical, II. The ability of overall antioxidant—the activity of TEAC, III. The activity test of inhibit Tyrosinase, and IV. The study of absorbing UV / VIS Spectrophotometers. This study use trolox, arbutin, and octyl salicylate as the control groups, and to test the ability of anti-oxidation, the activity of inhibit Tyrosinase, and the ability of absorbing UV. This research ultimately intends to investigate the applied value of those compounds into cosmetics.

本研究主要利用有机合成的方法，将不同数量及不同位置的羟基取代苯甲酸化合物与色洛冬宁进行醯胺化反应后，得到一系列的多羟基取代之N-色洛冬宁苯甲醯胺衍生物（化合物1 ~ 10），进行四种不同活性测试方法：一、清除DPPH自由基能力抗氧化活性测试；二、总抗氧化能力活性测试；三、抑制酪胺酸酶活性美白测试；四、紫外线／可见光光谱仪吸收测试，并以水溶性维生素E、熊果素、水杨酸辛酯当作对照组，探讨其抗氧化能力、抑制酪胺酸酶的活性能力与吸收紫外线能力，再进一步探讨其应用於化妆品上的价值。

For a big chunk of credit-card losses; the number of filings (and thus charge-off rates) would be rising again, whether

年美国个人破产法的一个改动使得破产登记急速下降，而后引起了信用卡大规模的亏损。

Eph. 4:23 And that you be renewed in the spirit of your mind

弗四23 而在你们心思的灵里得以更新