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aldehydes相关的网络例句

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与 aldehydes 相关的网络例句 [注:此内容来源于网络,仅供参考]

Cinnamaldehyde, a member of α,β-unsaturated aldehydes, and its semi- hydrogenated products such as cinnamyl alcohol and hydrocinnamaldehyde are important fine chemicals and intermediates especially in perfume industry and medicine manufacture.

肉桂醛是α,β-不饱和醛分子中的一种,肉桂醛分子中C=C键及C=O键加氢生成半加氢产物加氢肉桂醛和肉桂醇更是医药、香料等的重要原料及中间体。

The basic functionalized ionic liquid, 1 -butyl-3-methylimidazolium hydroxide OH, was prepared and used to catalyze the Knoevenagel condensation of aromatic aldehydes with malononitrile or ethyl cyanoacetate.

合成了碱性功能化离子液体氢氧化1-丁基-3-甲基咪唑,研究了将其作为催化剂催化芳香醛和丙二氰、氰基乙酸乙酯的Knoevenagel缩合反应。

The basic functionalized ionic liquid, 1-butyl-3-methylimidazolium hydroxide, was prepared and used to catalyze the Knoevenagel condensation of aromatic aldehydes with malononitrile or ethyl cyanoacetate.

合成了碱性功能化离子液体氢氧化1-丁基-3-甲基咪唑,研究了将其作为催化剂催化芳香醛和丙二氰、氰基乙酸乙酯的Knoevenagel缩合反应。

Knoevenagel condensation reaction of aromatic aldehydes with active methylene compounds like ethyl cyanoacetate proceeds smoothly in water in the presence of 8mol% of diammonium hydrogen phosphate and 2mol% TEBA.

醛与活泼亚甲基化合物的 Knoevenagel 反应是有机合成中广泛应用的形成碳碳键的重要方法,该反应一般是弱碱性催化剂存在下完成的,如各类胺、脲[1]等,Lerwis酸[2]、杂多酸[3]、氨基酸[4]等也可用于催化该反应。

In the second part of the thesis, we discussed a L-proline-catalyzed direct Aldol reaction between L-amino acid-derived N,N-dibenzyl -amino aldehydes 15 and acetone, cyclopentanone or hydroxyacetone, which afforded (-amino--hydroxy- or (-amino-,(-dihydroxy-ketones in good to excellent yields (up to 94%) and diastereoseletivities (up to 94.9%).

发现许多情况下,反应的产率和de值超过90%。接着,在碱性条件下,我们将L-亮氨酸衍生的N,N-二苄基--氨基醛15g与羟基丙酮反应得到的主要产物(,-二羟基-γ-氨基酮171d与次溴酸钠反应,得到了具有抗肿瘤活性的天然产物PM-94128的氨基酸片断184。

We have initially examined organocatalytic enantioselective synthesis ofα-Hydroxy phosphonates through the reaction of dialkyl phosphates and aldehydes.

我们初步实验了对映选择性的有机催化二烷基亚磷酸酯和醛的反应不对称合成α-羟基膦酸酯。

What's more, we expanded the reaction to aliphatic ketones and aldehydes undersimilar conditions and found that these reactions led to dialkyl diselenides underatmospheric pressure in the absence of base in from moderate to good yields.

在相同条件下,把底物扩展到杂环醛,也得到了一类相应的新的对称的杂环二硒醚,同时,把底物扩展到脂肪醛和脂肪酮,在类似条件下,也合成了一系列对称的烷基二硒醚,产率从中等到良好。

The third part of this thesis is reactive simulating calculation In this section, some well-known auxiliaries are selected to compute in density functional theory B3LYP on Gaussian 03, from which the relationship between reaction active energies of transition states and enantiomeric excess of chiral products homoallylic alcohols isobtained based on relative reactive ratio theory. Using this relationship, calculations on the reaction of more than eight auxiliaries with four other aldehydes are carried out in AMI and MNDO, proving that N,N\'-dibenzyl tartamide has higher enantioselectivity than others in this reaction.

第三部分为计算化学部分,运用密度泛函理论B3LYP方法在Gaussian03软件上对已经报道的几种手性配体参与的醛不对称烯丙基化反应过程进行模拟计算,基于相对反应速率理论找出两种构型过渡态间活化能的差异与产物光学收率之间的关系;并以此为基础,用AM1和MNDO方法对上述合成的几种配体控制的反应过程进行量化计算,从而在理论上证实了N-苄基酒石酸二酰胺配体在醛的不对称烯丙基化反应中具有较高的立体选择性。

The fluorescence images that RhoCr1 coordinated with Cr~(3+)in PC12 cells showed RhoCr1 to be capable of penetrating into living cells and imaging intracellular Cr~(3+)changesFive probes have been designed and synthesized,where different aldehydes were covalently linked to rhodamine B dyes with diethylamine flexible chains.

吸收和荧光光谱的测试结果表明,探针RhoCr1在Tris-HCI中性缓冲溶液中能高选择性的识别Cr~(3+)并产生了荧光增强,通过对探针光谱性能的测试和TEPN滴定实验表明,探针RhoCr1与Cr~(3+)的络合是一个可逆的过程。

From the point view of product distribution, conversion of dimethyl ether and energy consumption, with RCD plasma DME conversion was higher and was hardly affected by the residence time of dimethyl ether, and hydrogen, carbon monoxide and unsaturated hydrocarbons with RCD plasma were more than those with DBD plasma.There was no liquid product with RCD plasma, but the liquid product obtained with DBD plasma consisted of aldehydes, alcohols and methoxy-containing organic compounds, for instance, formaldehyde, methyl alcohol, dimethoxy ethane and so on.Moreover, most compositions of liquid product were methoxy-containing compounds, and the liquid product selectivity was as high as 32.23%.However, energy consumption for the reaction with DBD plasma was more than that with RCD plasma.

从产物分布、转化率及能耗上看,利用RCD所获得的二甲醚的转化率高,几乎不受二甲醚停留时间的影响,且氢气、一氧化碳和不饱和烃的含量大,几乎没有液相产物,而利用DBD能获得较多的液相产物,包括一些醇、醛和含有甲氧基的有机化合物,如甲醛、甲醇和二甲氧基乙烷,且大部分组成都是含有甲氧基的化合物,液相产物的选择性高达32.23%,但是能耗较大。

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