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hydroxy acid相关的网络例句

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与 hydroxy acid 相关的网络例句 [注:此内容来源于网络,仅供参考]

Results Seven known compounds: ocotillol (1), ursolic acid (2), betulin (3), lupeol (4), 1β-hydroxy-lupeol (5),β-sitosterol (6) and sitosterol-4-en-3-one (7) were isolated.

结果 分离得到7个化合物,分别鉴定为:20S,24R-环氧达玛烷-3β,25-二醇(ocotillol, 1)、熊果酸(2)、白桦脂醇(3)、羽扇豆醇(4)、1β-羟基羽扇豆醇(5)、β-谷甾醇(6)、谷甾-4-烯-3-酮(7)。

While PEG-1000 had worst liquefaction effect; its liquefied wood had higher acid value and hydroxy value. Wood liquefaction condition would influence the properties of PU foam.

由其结果得知,以PEG-400为液化药剂者有较佳之液化效果,其残渣率较低,以PEG-1000液化者效果较差,其液化木材有较高的酸价及羟价。

By chromatographic techniques. On the basis of physico-chemical properties and spectral data, they were identified as α-amyrin,α-amyrin acetate, 27-hydroxy-α-amyrin,β-amyrin,β-amyrin acetate, ursolic acid,β-sitosterol, dauricine, emodin.

中分离得到9个化合物,通过理化性质和光谱分析,分别鉴定为:α-香树脂醇,α-香树脂醇乙酸酯,27-羟基-α-香树脂醇,β-香树脂醇,β-香树脂醇乙酸醇,熊果酸,β-谷甾醇,β-胡萝卜甙,大黄素。

In this thesis, investigations focused on heteropoly acids-catalyzed C-C and C-N bond formation reactions and the synthesis of xanthenediones and acridinediones under thermal conditions are described.1.12-Phosphotungstic acid has been used as an efficient,eco-friendly,and air- and moisture-stable catalyst to promote the direct dehydrative substitution of the hydroxy group of benzylic and allylic alcohols with variousβ-dicarbonyl compounds.

本篇论文主要描述了杂多酸催化下的C-C和C-N键的生成,以及无溶剂直接加热下合成十氢氧杂蒽二酮和9-芳基十氢吖啶二酮。主要内容如下:1。在磷钨酸催化下,1,3-二羰基化合物与醇能够顺利偶合,脱除一分子的水,生成烷基化的1,3-二羰基化合物。反应在甲苯中进行时,二芳基甲醇能与各类1,3-二羰基化合物反应,成率很高;但对于1-苯乙醇,只能得到很低的产率。

Starting from 3, 5-dihydroxybenzoic acid, a total of 16 kinds of salicylicaldehyde derivatives have been synthesized by the esterification, substitution, reduction, formylation, condensation, brominate, functional group protection and deprotection reactions, of which 11 have not been reported yet. Enatiomerically pure 2-amino-2'-hydroxy-1, 1'-binaphthyl has been easily obtained from its racemic mixture by the eantioselective formation of inclusion crystals with N-benzylcinchoninium chloride.

树枝状大分子希夫碱三齿手性配体的设计与合成从3,5-二羟基苯甲酸出发,通过酯化、取代、还原、甲酰化、缩合、官能团的保护与去保护等反应合成了四个系列16种水杨醛衍生物,其中11中是未见文献报道的新化合物。

In comparison,the rhizobia in mature infected cells were larger,greater in number,varied in shape,and distributed throughout the nodule cells.The rhizobia in the mature cells also had poly-hydroxy butanoic acid and curapos.

成熟侵染细胞中,根瘤菌个体较大,数量较多,多呈棒状,少数为球形或椭球形,有很多根瘤菌还呈现明显的&T&形、&Y&形或&V&形,菌体占满了整个细胞,这时的根瘤菌大多数含有聚羟基丁酸和聚磷酸盐颗粒。

Their chemical structures were characterizd on the basis of spectral and chemical evidences to be: Sarracenin (1), 2-methyl-5-hydroxy-7-O-ethyl caffeate chromome (2), Naringenin(3), 2-methyl-5, 7-dihydroxychromome (4), 2-methyl-6-hydroxyl-cinnamic acid methyl ester (5), eriodictyol (6), quercetin (7), Naringenin-7-O-β-D-glucoside( 8 ), eriodictyol-7-O-α-D-glucoside (9), quercetin-3-O-β-D-glucoside(10). In addition, one compound was abtained from the n-butanol frationk, which was finally identified as Morrosiside(11) by spectral and chemical evidences.

以波谱数据及其理化性质鉴定为:Sarracenin(1),2-甲基-5-羟基-7-O-咖啡酸乙酯色原酮(2),柚皮素(3),2-甲基-5,7-二羟基色原酮(4),2-甲基-6-羟基苯丙烯酸甲酯(5),圣草酚(6),槲皮素(7),柚皮素-7-O-β-D-葡萄糖苷(Naringenin-7-O-β-D-glucoside)(8),圣草酚-7-O-α-D-葡萄糖苷(eriodictyol-7-O-α-D-glucoside)(9),槲皮素-3-O-β-D-葡萄糖苷(quercetin--3-O-β-D-glucoside)(10);另外从正丁醇萃取部位分离得到1个化合物,以波谱数据和文献对照鉴定为:Morroniside(11)。

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。

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。

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。

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