羟基化

The 1,5-Bis(4-aminophenylazo) anthraquinone, 1,5-bis(4-hydroxyphenyl azo) anthraquinone and 1,5-bis(3-methyl-4-hydroxyphe nylazo) anthraquinone were synthesized by diazotizing 1,5-biaminoanthraquinone with nitrosyl sulfuric acid and coupling with aniline, phenol and o-cresol.

合成以1，5-二氨基蒽醌为原料，经亚硝酰硫酸重氮化，分别和苯胺、苯酚及邻甲酚偶合，得到双（4-氨基苯）－1，5-二偶氮蒽醌，双（4-羟基苯）－1，5-二偶氮蒽醌和双（3-甲基－4-羟基苯）－1，5-二偶氮蒽醌，反应产率达47%~62%。

By the mechanism of the electrocyclic reaction, three groups of 4-hydroxy-2-cyclobutenones 4 were designed and synthesized to investigate their behaviors underthe thermolysis conditions Meanwhile, a new procedure for preparation of 2(5H)-furanone 5 Was discovered.

根据电环化反应机理，我们设计了三组不同类型的4-羟基-2-环丁烯酮(4)。通过对4-羟基-2-环丁烯酮(4)进行热解，发现了一种制备2(5H)-呋喃酮类化合物(5)的新方法。

Compound 9 is glycosylated in the presence of TMSOTf with rhamose-derived trichloroacetimidates to provide target trisaccharide Saponin 1, oleanolic acid 3-yl-2,4-di-O-a-L-rhamnopyranosyl -p-D-glucopyranosideCoumpond 18 is prepared with oleanic acid and Bromide 11 through phase-thansfer catalysis glycosylation manner.

三糖皂苷Saponin 1是以葡萄糖齐墩果酸皂苷为起始原料，用BBTZ(1-苯甲酰苯并噻唑)选择性保护葡萄糖3′，6′-羟基得到化合物9，然后以化合物9为糖基受体，进行一步糖苷化可以在化合物9的2′，4′-羟基上同时引入两分子鼠李糖，最后脱掉所有的保护基得到目标化合物Saponin1。

Therefore esterification crosslinked reactionbetween polyearboxylic acid and wood can be quantitatively determined.According toexperiment results of stereoscopic configuration choices by crosslinking agents,crosslinkingreaction between model of reaction intermediate and wood,and the intermediate characteristic incrosslinking reaction,crosslinking reaction intermediate was proofed.We can infercrosslinking reactions between polycarboxylicacid and wood want through a mechanism of twosteps reaction process,the first cyclic anhydrides were formed as intermediates by dehydratingbetween hydroxyls in polycarboxylic acids,second esters were occurred by substitution reactionbetween wood hydroxyls and cyclic anhydrides.

从而可全面定量表征木材与多元羧酸类化合物的酯化交联反应；依据交联剂立体构型选择性、反应中间体模型物与木材的交联反应和交联反应中间体的波谱特征实验结果，证实了交联反应中间体，因此可以推测：多元羧酸类化合物与木材化学组分的交联反应是经历两步反应的机理，首先多元羧酸中相邻羧基的羟基之间脱水形成五元环酸酐中间体，然后木材的羟基与酸酐发生亲核取代反应形成酯。

In this article, the preparation of benzyl 4-hydroxybenzoate in water was reported, with 4-hydroxybenzoic acid and benzyl chloride as main raw materials, cetyl trimthylamonium bromide as phrase transfer catalyst.

采用改进工艺，以正十六烷基三甲基溴化铵为相转移催化剂，水为溶剂，对羟基苯甲酸和氯化苄为主要原料，合成对羟基苯甲酸苄酯。

The real-time quantitative PCR results showed that the expression level of two genes did not be affected by HHO obviously, whereas, the expression level of CHS gene had down regulation of different degree, except in 1.0 mM of HHO's concentration. It meaned that CHS gene is probably related with the metabolism of allelochemical.4. The Chalcone synthase gene (EaCHS1) of E.

荧光定量PCR的结果表明，萜类代谢途径中的两个关键酶基因的表达水平，没有因为羟基泽兰酮的诱导而表现出显著的差异；CHS基因的表达水平，除了在羟基泽兰酮处理浓度为1.0 mM时的差异不显著之外，在其他处理浓度均有不同程度的下调，说明该基因与化感物质的代谢途径相关。4。

The invention is characterized in that the molecule of the polymer adsorption material has a structure in formula I: in the formula, R is selected from the natural polysaccharides with amino groups and hydroxyls and the derivatives thereof or the chemosynthetic polymers, the molecular weight of which is from 6 KD to 500 KD; X is selected from a C0 to C6 paraffinic chain with O atoms, N atoms or OH groups; R1, R2 and R3 are selected from a C1 to C4 alkyl group.

生物医学材料领域中的水溶性阳离子多聚物吸附材料及其应用，包括采用带有氨基或羟基的天然多糖及其衍生物或者化学合成多聚物季铵化反应合成，其特征在于该多聚物吸附材料分子具有式的结构：式中，R选自粘均分子量范围为6KD～500KD的带有氨基或羟基的天然多糖及其衍生物或者化学合成多聚物；X选自含有O原子、N原子或者OH基团的C 0 ～C 6 烷链；R 1 、R 2 、R 3 选自C 1 ～C 4 的烷基。

The new synthetic technology of some important anthraquinone intermediates derived from 1-amino- anthraquinone, l-amino-4-hydroxy-anthraquinone, l-amino-4-bromo- anthraquinone-2-sulfonic acid, 1,5- and 1,8 dinitro- anthraquinone, have been studied.

本文研究了几种重要的由1-氨基蒽醌衍生的蒽醌型中间体：1-氨基-4-羟基蒽醌、1-氨基-4-溴蒽醌-2-磺酸和1，5-及1，8-二硝基蒽醌的合成化学，在此基础上开发了上述中间体的合成新技术。现行1-氨基-4-羟基蒽醌的生产技术是从1-氨基蒽醌出发，经二溴化再水解制得，溴的耗量在1.5mol以上。

According to the distribution of the positive charges inthe surface of the cage, it can be expected that two -OH groups finally adding at two sites which arewithin one hexacyclic ring and in different sides of equator, which is accord with the conclusion resultedfrom thermodynamics

通过寻找并分析过度态的结构，发现酸化阳离子中处于赤道带6-6类碳原子上的羟基和两极区域5-5类碳原子上的羟基都有朝邻近赤道带碳原子上迁移的可能，结合碳笼上正电荷的分布特征，预计亲核水解作用将发生在赤道异侧六员环的对位，说明考虑动力学因素，最终获得1，4-加成富勒醇的可能性最大，该结论与热力学的结果一致。

In the first chapter, Barton reaction of C〓-hydroxy was studied.

论文第二部分分两章，第一章主要考察了甾体C〓-羟基的Barton反应，期望通过C〓-羟基的Barton反应进行18-甲基的官能团化。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。