乙二醇

Dihydroxy-7, 4′-dimethoxy-dihydrflavonol and -3, 5, 7 -trihydroxy-4′-methoxy- dihydrflavonol were synthesized by selective protection, condensation, epoxidation, cyclization and deprotection from 2, 4, 6-trihydroxyacetophone and anisaldehyde.

以2，4，6-三羟基苯乙酮和茴香醛为起始原料，经选择性保护、缩合、环氧化、关环等步骤首次完成了-3，5-二羟基-7，4′-二甲氧基二氢黄酮醇和-3，5，7-三羟基-4′-甲氧基二氢黄酮醇全合成。

The control group were fed basal diet, group 1 to 3 were fed basal diet supplemented with 90,100,110 mg/kg of Lespedeza Bicolor crude extract, group 4 to 6 were fed basal diet supplemented with 60,70,80 mg/kg of ethyl acetate extract, group 7 to 9 were fed basal diet supplemented with 60,70,80 mg/kg of n-butanol extract.

试验期42 d。对照组饲喂基础日粮，1～3 组饲喂基础日粮加二色胡枝子粗提物90、100、110 mg/kg；4～6 组饲喂基础日粮加二色胡枝子乙酸乙酯萃取物60、70、80 mg/kg；7～9 组饲喂基础日粮加二色胡枝子正丁醇萃取物60、70、80 mg/kg。

The obtained results show that the primary and secondary alcohols areconverted in good yields, whereas tertiary alcohol and phenol are unreactive.

当原料分别为乙醇、正丁醇、仲丁醇、苯甲醇和苯乙醇时，目标产物碳酸二乙酯、正丁基乙基碳酸酯、仲丁基乙基碳酸酯、苯甲基乙基碳酸酯和苯乙基乙基碳酸酯的产率分别为67.3、52.3、56.7、37.6和32.8％。

Yields from chiral bisoxazolines (5a) with diethyl oxalate using NaOCH〓 as base for the first time. The structures of chiral multioxazolines and their intermediates, multi (β-hydroxylamide) s, were characterized by 〓H NMR, IR, mass spectra and elemental analysis. The catalytic activities and enantioselectivities of chiral multi (β-hydroxylamide) s (4) and chiral multioxazolines (5～8) were investigated by using acetophenone and β-acetonaphthone as former chiral ketone, KBH〓 or NaBH〓 as reductive reagent in chapter three.

在此基础上，对合成方法作了创新，以羧酸或酯为原料，在无催化剂的条件下与手性α-氨基醇反应，通过回流分水或脱醇的方法，一步反应合成了手性多噁唑啉（5～8），产率为89.2%～98.4%；以手性双噁唑啉（5a）为原料，在NaOCH〓的作用下，与草酸二乙酯反应，首次合成了呋喃类双嗯唑啉（6a），产率为72.9%～75.6%。

Seven compounds have been isolated from hard coral Acropora pulchra. These compounds are:pentadecoic acid, heptadecyl ester;(2)n-cetanol;(3)batyl alcohol;(4) N- [ 1 --2-hydroxyl--3,7-heptad-ecadienal] -hexadecanamide;(5)1 -0-hexanoyl-glycerol ester;(6)thymine;(7)uracil. Their structures were determined by IR, MS, HNMR, 13CNMR analysis.

从北海佳丽鹿角珊瑚Acropora pulchra乙醇提取液的乙酸乙酯部分分离出七个化合物，经IR、MS、~1HNMR、~(13)CNMR等波谱方法鉴定，其结构分别为：(1)十五酸十七酯，(2)正十六碳醇，(3)鲨肝醇，(4)N-1-羟基甲基-2-羟基—-3，7-十七碳二烯基十六酸酰胺，(5)1-正十六酸甘油酯，(6)胸腺嘧啶，(7)尿嘧啶。

For the synthesis reaction of chalcone, cyclohexanone aldolization and biodiesel,γ-Al_2O_3-NaOH-Na solid superacid has a satisfactory catalytic activity. With hypnone and phenylaldehyde as raw material, amount of catalyst 7.5% wt% of material, mole ratio of hypnone and phenylaldehyde 1:1.1, reaction temperature 40℃, after 3 hours, the yield of chalcone can be up to 96.88%. With cyclohexanone as raw material, amount of catalyst 10% wt% of material, reaction temperature 190℃, after 3 hours, dimmer of cyclohexanone can be up to 85.66%.

将该固体超强碱催化剂应用于查尔酮、环己酮自缩合以及生物柴油的合成反应中，该改性固体超强碱催化剂表现出了良好的催化活性：以苯乙酮和苯甲醛为原料，反应温度为40℃，催化剂用量为反应物总质量的7.5％，苯甲醛与苯乙酮摩尔比为1：1.1，反应3h查尔酮产率可达96.88％；以环已酮为原料，催化剂用量为原料总质量的10％，反应温度为190℃，反应3h，二聚物的总收率可达85.66％；以动物油和甲醇为原料，醇油摩尔为9：1，催化剂用量为动物油质量的2％，反应温度为70℃，反应3h后，生物柴油的收率可达91.8％。

Thermodynamic properties of PSf - DMAc - alcohols ternary systems are studied, the binodal is calculated. Cloud point curves from light scattering experiment verify the calculation results; The agreement between the cloud point curves and the binodal is quite well.

文章摘要：对聚砜-二甲基乙酰胺-醇类非溶剂构成的制膜体系的热力学特性进行了研究，计算出这些体系的双结点线，并用这些醇类非溶剂通过光散射法进行浊点滴定实验，浊点曲线与双结点线基本重合，验证了双结点线的计算结果。

Methods A mixture of 10 mol/L potassium dihydrogen phosphate solution and acetonitrile(60 ∶ 40) was used as the mobile phase.

方法以乙腈-10mmol/L磷酸二氢钾(40∶60)为流动相，炔雌醇为内标，血浆样品经乙酸乙酯萃取。

In this study, new benzo[l,2,3]thiadiazole derivatives were designed according to relationship of structure and efficacy. The 9 novel compounds were synsthesized with following reactions. The chlorine atom in 2-chloro-3,5-dinitro-benzoic acid as beginning raw material was substituted by 2-methylpropane-2-thiol, esterified then with bromoethane, reduced by iron powder and cyclized to obtain ethyl benzo[l,2,3]thiadiazole-7 after diazonation reation.

本论文根据苯并噻二唑诱导剂的构效关系设计了新的苯并噻二唑的结构，并合成了9个未见文献报道的化合物，合成步骤如下：采用2-氯-3，5-二硝基苯甲酸为起始原料，苯环上的氯原子被叔丁基硫醇置换，羧酸由溴乙烷酯化，硝基由铁粉还原，随后经重氮化关环生成苯并[1，2，3]噻二唑-7-羧酸乙酯。

Three fullerene derivatives including a bisadduct of tetraethyl methano[60] fullerenediphosphona- te、a dimalonic acid[60]fullerene (DMA C60and fullerol were used to study the relationship between their photo-induced GSH depletion and structures.

采用二加成亚甲基富勒烯[60]二膦酸四乙酯、二加成富勒烯[60]丙二酸(DMA C60)和富勒醇 3种富勒烯衍生物研究富勒烯衍生物的结构与光诱导细胞内GSH耗竭的关系。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。