生产了各种芳基三氟甲磺酸酯。
他开发了光致变色材料的二芳基乙烯系列。
He developed the diarylethene family of photochromic materials.
可用于合成各种具芳基胺醇类结构的手性药物。
It can be oriented to produce levo-aromatic and dextro-aromatic alcohols.
详细研究了氟代苯基硼酸和多芳基硼酸的合成及其工艺改进。
The synthesis of fluoro-substituted phenylboronic acid, and multiarylboronic acid and their process improvement were studied in detail.
例如芳基二硫化物可抑制聚烯烃的氧化。
结果：合成得到5个二芳基庚烷类衍生物。
二芳基氮氧化物比二烷基氮氧化物还要稳定。
Diaryl nitroxides are even more stable than the dialkyl nitroxides.
芳基烷酸类及其他结构类型的非甾体抗炎药。
This section focuses on pyrazole ketones, indole acetic acids, aryl alkyl acids non-steroidal anti-inflammatory drugs.
因此，与芳基取代的烯丙基碳酸反应选择性。
Thus, the reaction with aryl-substituted allylic carbonates is regioselective.
取代芳基膦酸盐是最重要的聚丙烯成核剂之一。
Substituted aromatic phosphate is one of the most important nucleating agents for polypropylene.
芳基取代聚炔及其衍生物呈现出光电磁等许多新颖的性能。
Aryl substituted polyacetylenes and their derivatives exhibit a lot of novel optical, electric, magnetic properties.
目的研究多芳基取代蝶啶类化合物的合成及其抗肿瘤活性。
Aim To study the synthesis and antitumour activities of some aryl-substituted pteridines.
二芳基氮氧化物自由基比二烷基氮氧化物自由基还要稳定。
Diaryl nitroxides are even more stable than the dialkyl nitroxides.
这是第一个用芳基硼酸的磷光光谱对单糖进行识别的研究。
This was the first time to use phosphorescence spectra of aromatic boronic acid for the recognition of carbohydrates.
芳基叔膦和金属锂在超声波辐射下迅速反应产生芳基膦锂。
The fragmentation reaction of aryl tertiary phosphines in the presence of lithium can be promoted effectively by use of ultrasonic irradiation.
联芳基取代吡唑化合物为钠通道阻滞剂，用于治疗疼痛和其它病症。
Biaryl substituted pyrazole compounds are sodium channel blockers useful for the treatment of pain and other conditions.
本文研究在氢氧化铯催化下，三甲硅基乙炔与二芳基二硒醚的反应。
It has been researched on the reaction of trimethylsilylacetylene with diphenyl diselenide catalyzed by cesium hydroxide.
提出了一种合成芳基氟喹诺酮抗菌剂二氟沙星和替马沙星的新方法。
A new synthetic method for preparing two arylfluoroquinolone antimicrobial agents, difloxacin and temafloxacin, was reported.
芳基柔性二齿配体的配位构型多变，使得其金属配合物的结构丰富多彩。
Self assembly of aryl group containing flexible bidentate ligands with metal ions gives rise to many types of novel structures because of their variable coordination modes.
联芳基取代的吡啶、嘧啶和吡嗪化合物为用于治疗疼痛的钠通道阻滞剂。
Biaryl substituted pyridine, pyrimidine and pyrazine compounds are sodium channel blockers useful for the treatment of pain.
由芳基锂盐、硫代甲酰胺和芳基格氏试剂一锅法合成了取代二芳基甲胺。
One-pot synthesis method of diarylmethylamines was investigated using aryl lithium salt, thioformamide and aryl Grignard reagent.
用作高选择性环加氧酶-2抑制剂的二芳基1,2,4 -三唑衍生物。
Diaryl 1, 2, 4-triazole derivatives as a highly selective cyclooxygenase-2 inhibitor.
通过明胶活泼氨基的酰化反应，可以接入憎水性的芳基改变明胶的水溶性；
The amino groups of the gelatin are the amenable sites for modification in aqueous solution. Benzoylation of the gelatin with pathalic anhydride can change the solubility.
芳基肟胺菊酯类化合物和1，2，4-恶二唑衍生物的合成及其生物活性研究。
Studies on the Synthesis and Biological Activities of Aryl Amidoximyl Chrysanthemumates and 1,2,4-Oxadiazole Derivatives.
目的探讨5 ，6二芳基2 ，3二氢1吡咯里嗪酮类化合物的作用机制。
AIM To theoretically explore the mechanism of action of 5,6 diaryl 2,3 dihydro 1 pyrrolizinone derivatives.
在此条件下，苯乙烯单程转化率可达93.5%，二芳基乙烷的选择性为78.9%。
Styrene conversion of 93.5% and selectivity to diphenylethylane of 78.9% were attained under the optimum condition.
本论文对二芳基庚烷类天然产物的分布，生物活性，生物合成及化学合成进行了概述。
This thesis describes natural diarylheptanoids from distribution, bioactivity, biosynthesis and synthesis and focuses on the synthesis of several diarylheptanoids.
当然，人们也观察到了通过芳香C—H键活化产生的芳基碳钯键与腈基的分子间反应。
In- termolecular reactions were observed with the C—Pd bond formed by the C—H activation of the aromatic ring and the nitrile group.
尤其，对于沿着聚合物主链带有芳基的聚合物通常有至少约55%的芳环位置被氟化。
In particular, for polymers with the aromatic groups along the polymer backbone generally at least about 55 percent of the aromatic ring positions are fluorinated.
研究了数种芳基甲烷在有机溶剂中碱催化下的氧化缩合反应，并对反应产物进行了表征。
Oxidative dimerizations of a seris of aryl methanes have been investigated and the products characterized.
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