查询词典 morphologic synthesis

3 The effects of APS and AstragalosideⅣon synthesis of collagen Measure the Radix Astragali impact on NIH3T3 cells collagenic synthesis of many candies with the hydroxyproline reagent box.

2.3黄芪多糖和黄芪甲苷对胶原合成的影响本实验以NIH3T3为细胞模型，用羟脯氨酸试剂盒测量黄芪多糖对NIH3T3细胞胶原合成作用的影响。

Through activating the synthesis of jasmonic acid itself,aboveground application of jasmonia acid could induce the expression of Bx1,Bx9,PAL,PR-1,MPI,FPS and TPS genes,increase DIMBOA content and decrease caffeic acid content in leaves;on the other hand,the systematic induction of gene expression of Bx6,Bx9、PAL and PR-2a,increase of contents of coumaric acid and caffeic acid,and decrease of syringic acid content in the roots were related with the activating of jasmonic acid synthesis in the aboveground.

茉莉酸处理地上部是通过激活茉莉酸自身合成来诱导叶片Bx1、Bx9、PAL、PR-1、MPI、FPS和TPS基因的表达、增加叶片丁布含量及降低咖啡酸含量的，同时系统诱导根系Bx6、Bx9、PAL和PR-2a基因表达、增加香豆酸和咖啡酸含量以及降低丁香酸含量则与激活地上部茉莉酸自身合成相关。

These indicted that the low temperature in autumn and short sunshine could promote the synthesis of the leaf protein,degrade the buildup of starch and invert part of starch to glucose,thus the PAL enzymatic activity were increased and the synthesis of cyanin was promoted,the leaf color changed red.

这说明秋季低温和短日照促进叶片蛋白质的合成，降低淀粉积累，将部分淀粉转化为葡萄糖，PAL酶活性增加，从而促进花色素苷的合成，叶色转为红色。

The synthesis of 4,5,7-trichloroquinoline makes use of ethyl orthoformate, cyanoacetic ester and 3,5-dichloroaniline as the raw materials. The synthesis is completed by four steps: condensation, cyclization, hydrolyzation and chlorination. Several conditions concerned in the process are studied, the whole yield of 4,5,7-trichloroquinoline is about 53%, and the purity of it is about 96%. All the products are testified by IR, NMR and HPLC.

介绍了以3，5-二氯苯胺、原甲酸三乙酯和氰乙酸乙酯为原料，经过缩合、成环、水解和氯代4步反应制备4，5，7-三氯喹啉的方法，对相关的试验条件进行了考察，通过红外光谱、核磁共振谱和液相色谱对4，5，7-三氯喹啉的结构和纯度进行表征和测定，试验结果为4，5，7-三氯喹啉的纯度大于96%，总收率达到53%。

This work, concentrated on the asymmetric allylation of aldehydes controlled by different chiral auxiliaries prepared from rotational pure tartaric acid, can be divided into three parts.The first part aims to review the developments of chiral drugs and asymmetric synthesis, from which derived the present research topic backgrounds and works.Synthesis and applications of allylation from aldehydes are the second part of the thesis. By optimizing the reaction conditions, such as solvents, temperature, time and chiral auxiliaries like N,N\'-dibenzyl tartamide, N,N\'-p-dimethylphenyl tartamide, N,N\'-o-dimethylphenyl tartamide, N,N\'-o-dichlorophenyl tartamide, N,N\'-a-dinaphyl tartamide, N,N\'-dicyclohexyl tartamide and N,N\'-diphenyl tartamide, ideal experimenttal conditions are obtained according to HPLC monitoring, as well as the auxiliaries\' recoveries experiments. Starting from benzaldehyde and 3-bromopropaldehyde, N,N\'-dibenzyl tartamide is considered the best auxiliary in this reaction.

本文介绍了醛的不对称烯丙基化反应，以光学纯酒石酸为原料，研究了不同构型手性配体在醛的烯丙基化反应中的立体选择性，全文共分三部分十个章节：第一部分对当前手性药物和手性技术进行了概述，并由此展开了本文的研究背景和任务；第二部分为有机合成部分，对醛的不对称烯丙基化反应进行了深入探讨，以苯甲醛为原料对反应条件进行优化，在优化的反应条件下对制备的七种可回收手性酰胺配体(N-苄基酒石酸二酰胺、N-对甲苯基酒石酸二酰胺、N-邻甲苯基酒石酸二酰胺、N-邻氯苯基酒石酸二酰胺、N-a-萘基酒石酸二酰胺、N-环己基酒石酸二酰胺和N-苯基酒石酸二酰胺)进行筛选，优化配体回收实验条件，最终确定出N-苄基酒石酸二酰胺在苯甲醛的不对称烯丙基化反应中具有较大优越性，结晶回收的手性配体光学纯度保持不变。

Reaction of 5'-O-p-methoxytrityl-thymidine with 1, 1'-carbonyl-diimidazole gave the 3'-O-carbonylimidazolide, which was condensed in high yield with 3'-O-protected thymidine to give a dithymidine carbonate. In the same way, we obtained the protected trithymidine dicarbonate. After deprotection, we obtained quantatively the trithymidine dicarbonate.By the same stratagy, we completed the synthesis of dithymidine sulfite.It was shown that allyl can be used as a good protection group for hydroxyl of ribose in the synthesis of oligonucleotides consisting in some unstable nucleotide analogues.

我们在第一部分工作的基础上，以烯丙基作为3'-OH的保护基合成了保护的三胸苷碳酸酯以及二胸苷亚硫酸酯，用我们所得的脱保护条件进行了脱保护研究，得到了三胸苷碳酸酯以及二胸苷亚硫酸酯，并研究了它们合成中的一些化学问题，结果表明：烯丙基能很好地运用于这两类寡核苷酸类似物的合成中，其脱保护条件为中性，不会影响碳酸酯键及亚硫酸酯键。

Ytterbium metal, ytterbium diiodide, samarium diiodide promoted organic reaction and their applications in organic synthesis;;bis carbonate in organic synthesis

中文题名金属镱，二碘化镱和二碘化钐促进的有机反应在有机合成中的应用；双碳酸酯在有机合成中的应用

The chapter two was focused on the samarium diiodide promoted organic reactions and their applications in organic synthesis, firstly, a new synthesis of highly substituted cyclopentadienes from a,β-alkynone promoted by samarium diiodide was investigated and the highly substituted cyclopentadienes were prepared in moderate to good yields under mild conditions. Secondly, the Michael addition and Michael-aldol tandem reaction of diorganyl diselenides or diorganyl disulfides with α,β-alkynones mediated by samarium diiodide were studied and a series of alkenylsulfides and alkenylselenides were prepared in good yields. Then the highly regioselecfive nucleophilic addition of the allylsamarium bromide to α,β-alkynones were explored. We found that the allylsamarium bromide reacts with α,β-alkynones to afford regiospecificly 1. 2-nucleophilic addition products in good yields under mild condition. At last we studied the coupling reaction of aryl halides promoted by NiCl〓/PPh〓/Sm〓.

第二章 研究了二碘化钐、金属钐促进的有机反应：1、二碘化钐促进下α，β-炔基酮的偶联环化反应，提供了一种制备多取代环戊二烯的新方法；2、二碘化钐促进下的二硫醚、二硒醚与α，β-炔基酮的Michael加成反应，为高产率地制备多取代的烯基硫或烯基硒化合物提供了方便可靠的新方法；3、二碘化钐促进下的二硫醚、二硒醚与α，β-炔基酮和醛、酮的Michael—aldol串联反应，提供了一种一锅法高产率地制备多取代的含硫的烯丙基醇或含硒的烯丙基醇类化合物的方便可靠的原子经济性的新方法；4、烯丙基溴化钐与α，β-炔基酮的高度区域选择性的1，2-亲核加成反应；5、NiCl〓/PPh〓/Sm〓促进的卤代芳烃的偶联反应-一种从各种卤代芳烃制备联苯类化合物的有效方法。

According to the structure and synthesis character of the geminal dinitro energetic plasticizers,the current situation about the synthesis,the property and application of geminal dinitro aldehyde acetals,esters and ether energetic plasticizers is summarized with 21 references.

从偕二硝基含能增塑剂的结构和合成特点出发，综述了偕二硝基缩醛类、酯类及醚类等含能增塑剂的合成、性能及应用研究现状。

In the forth part of the dissertation, based on the mechanism of classical Strecker reaction,we developeda new method for the asymmetric synthesis of the α,α-disubstituted amino acid, and applied it to theasymmetric synthesis of-αM4CPG, compound 11a and 11b.

在本论文的第四部分，我们从深入分析经典的Strecker反应入手，发展了一条新的以酮为原料出发的立体选择性地合成α，α-双取代的光学纯的氨基酸的方法，并且利用该方法立体选择性地合成了化合物-αM4CPG，11a和11b。

There had been a moment during the breakfast meeting, though, after the backslapping and the small talk and when all of us were seated, with Vice President Cheney eating his eggs Benedict impassively and Karl Rove at the far end of the table discreetly checking his BlackBerry, that I witnessed a different side of the man.

那次早餐会期间，在表示过关心和寒暄以后，我们所有人坐了下来，我注意观察了一下，副总统切尼面无表情地吃着班尼迪克蛋（Eggs benedict，源自美国，以英式松饼、火腿、水煮蛋以及荷兰酱组合而成），卡尔。罗夫在餐桌的远端谨慎地经常查看他的黑莓手机，我目睹了他所不为人知的一面。

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