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双语推荐:二酮

高顺式一氢茉莉酸甲酯作为香料其性能远优于普通氢茉莉酸甲酯,是各大型香精香料公司的招牌产品之一。脱氢氢茉莉酸甲酯是合成高顺-氢茉莉酸甲酯的中间体。以普通氢茉莉酸甲酯为初始原料,IV一溴代丁酰亚胺作为溴代试剂,三乙胺为脱溴试剂,制得脱氢氢茉莉酸甲酯
High cis-dihydrojasmanate,a noble fragrance,is often one of a pride for a FlaVor_fragrance company. Tht methyl dehydrodihydrojasmonate is a Intermediate synthesizes the High cis-dihydrojasmanate.The methyl dehydrodihydrojasmonate is syn-thesized from original methyl dihydrojasmonate via bromination,de-hydrobromination and hydrogenation. The N-bromo-succini-mine was employed in the bromination reaction.The methyl dehy-drojasmonate was prepared,while the Sodium methoxide was em-ployeas the dehydrobromination regants.
以甲基丙烯酸-N,N-甲基氨基乙酯为亲核试剂,分别与4-溴甲基苯甲和4,4’-(溴甲基)苯甲在20℃下反应,并过简单的过滤,得到了两种水性可聚合苯甲类光引发剂:4-[N-(2-甲基丙烯酰氧基乙基)甲基溴化铵甲基]苯甲(收率79.2%)和4,4’-双[N-(2-甲基丙烯酰氧基乙基)甲基溴化铵甲基]苯甲(收率79.7%)。产物用NMR、IR和元素分析进行了表征。
Two novel water-soluble polymeric benzophenone photoinitiators were efficiently synthesized at 20℃by using 2-( Dimeth-ylamino)ethyl methacrylate,4-bromomethyl benzophenone,and 4,4′-di(bromomethyl)benzophenone as reactants,respectively.The yield of 4-[N-(2-methacyloxylethyl)dimethylammonium methyl]benzophenone was 79.2%,and that of 4,4′-bis[N-(2-methacylox-ylethyl)dimethylammonium methyl]benzophenone was 79.7%.The products were characterized by IR,NMR and EA.

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以芳香醛和为原料,合成了3类姜黄素类1,5-芳基-1,4-戊烯-3-衍生物:1,5-噻吩基-1,4-戊烯-3-(Ⅰ)、1,5-苯基-1,4-戊烯-3-类(Ⅱ)和1,5-呋喃基-1,4-戊烯-3-(Ⅲ);利用元素分析、红外光谱、核磁共振谱(1 H NMR及13 C NMR)分析了产物的组成和结构,初步探讨了其反应条件和反应机理.结果表明,以无水乙醇为溶剂、8%的NaOH溶液为催化剂,反应温度为30~50℃时,反应产率较高.
T hree kinds of curcumin-type 1 ,5-diaryl-1 ,4-pentadien-3-one derivatives , 1 ,5-bis (3′-methyl-2′-thienyl )-1 ,4-pentadiene-3-ketone (Ⅰ ) , 1 ,5-diphenyl-1 ,4-pentadiene-3-ketone (Ⅱ) and 1 ,5-furyl-1 ,4-pentadiene-3-ketone (Ⅲ ) were designed and synthesized with aromatic aldehyde and ketone as the raw materials . T he composition and structure of as-synthesized products were characterized by elemental analysis ,infrared spectrometry and nuclear magnetic resonance (1 H NMR ,13C NMR) spectroscopy .Moreover ,the reaction conditions and reaction mechanisms were preliminarily discussed .Results show that target products can be obtained in relatively high yield at 30-50 ℃ in the presence of ethanol as the solvent and 8% NaOH solu-tion as the catalyst .

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目的研究17β雌醇对氯胺所致原代培养皮质神经元凋亡的影响及其机制。方法原代培养皮质神经元,体外培养7 d,随机分为空白对照组(给予相同体积的DMSO),雌醇组(17β雌醇终浓度为0.1μmol·L-1),氯胺组(氯胺终浓度为100μmol·L-1),氯胺+雌醇组(氯胺,17β雌醇终浓度分别为100μmol·L-1,0.1μmol·L-1)。噻唑蓝(MTT)法检测神经元存活率,Hoechest33258染色法检测皮质神经元凋亡,Western-blot法测定cleaved-Caspase-3及Bcl-2蛋白表达。结果氯胺组神经元存活率(54.02±7.78)%,明显低于空白对照组;氯胺+雌醇组神经元存活率(88.09±6.54)%,明显高于氯胺组。神经元经Hoechest33258染色在荧光显微镜下观察,氯胺组神经元凋亡[凋亡率(49.50±4.34)%]较空白对照组明显增加,氯胺+雌醇组[凋亡率(15.74±3.40)%]较氯胺组神经元凋亡下降。氯胺组cleaved-Caspase-3表达明显增加,Bcl-2明显下降,而氯胺+雌醇组较氯胺组cleaved-Caspase-3表达明显下降,Bcl-2表达明显升高。结论 17β雌醇通过抑制神经元凋亡对抗氯胺诱导的皮质神经元损伤,产生保护作用。
Objective To investigate the protective effect and the mechanisms of 17β-estradiol on ketamine-induced apoptosis on primary cultured rat cortical neurons. Methods Cortical neurons were primarily cultured for seven days,then divided into four groups :control group ( treated with equal valume of DMSO ),estradiol-treated group ( treated with 0.1 μmol·L-1 17β-estradiol),ketamine-treated group(treated with 100 μmol·L-1 ketamine),ketamine plus 17β-estradiol-treated group( treated with 0. 1 μmol·L-1 17β-estradiol+100μmol·L-1 ketamine). The neurons were treated for 24 hours. The neuron viability was determined by MTT. Neuroapoptosis was measured by nuclear morphometry after Hoechest 33258 dying. Western blotting was performed to detect the expression levels of cleaved-caspase-3 and Bcl-2protein. Results The neuron viability in the ketamine group was(54. 02±7. 78)%,significantly decreased from the control group,whereas ketamine plus 17β-estradiol increased the cell viabi

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对远志进行化学成分研究.方法:采用硅胶柱色谱、Sephadex LH-20、大孔吸附树脂等方法进行分离纯化,根据化合物的波谱数据确定化合物结构.结果:从远志氯仿部位分离并鉴定了8个化合物,分别为:7-羟基-1-甲氧基-2,3-亚甲氧基(咄)(1)、1,7-羟基-2,3-甲氧基(咄)(2)、1,3,6-三羟基-2,7-甲氧基(咄)(3)、7-羟基-1,2,3-三甲氧基(咄)(4)、1,2,3,6,7-五甲氧基(咄)(5)、1,3,7-三羟基-2,6-甲氧基(咄)(6)、7-羟基-1-甲氧基(咄)(7)、1,7-羟基-3,4-甲氧基(咄)(8).结论:其中,化合物1、6~8为首次从该植物中分离得到.
Objective:To study the chemical constituents from the root of Polygala tenuifolia.Methods:Silica gel,Sephadex LH-20 and ODS chromatographic techniques were used to study the chemical constituents of Polygala tenuifolia,and the chemical structures were elucidated by application of spectral data.Results:Eight compounds were obtained and their structure were identified as 7-hydroxy1-methoxy-2,3-methylenedioxyxanthone (1),1,7-dihydroxy-2,3-dimethoxyxanth one (2),1,3,6-trihydroxy-2,7-dimethoxyxanthone (3),7-hydroxy-1,2,3-trimethoxyxanthone (4),1,2,3,6,7-pentamethoxyxanthone (5),1,3,7-trihydroxy-2,6-dimethanoxyxanthone (6),7-hydroxy-1-methoxyxanthone(7) and 1,7-dihydroxy-3,4-dimethoxyxanthone(8).Conclusion:Compounds 1,6,7 and 8 are isolated from Polygala tenuifolia for the first time.

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探讨高血压脑出血患者血清雌醇、睾水平与病情程度及预后的相关性。方法:检测168例高血压脑出血患者(脑出血组)及60例对照组血清雌醇、睾的含量,按美国国立卫生研究院卒中量表标准对患者进行评分,再按病情轻重及病程评分的差值分组比较。结果:男性脑出血组雌醇和睾与对照组差异均有统计学意义(P0.01和P0.05),男女脑出血组雌醇/睾比值与对照组差异均无统计学意义(P0.05)。男性患者轻度病情组血清雌醇含量较中、重度组升高(P0.05),男性3种病情组雌醇/睾比值差异均无统计学意义(P0.05)。男性患者少量出血组血清雌醇和睾含量均较中量出血组升高(P0.05),男性3种出血组雌醇/睾比值差异均无统计学意义(P0.05)。女性脑出血组雌醇与对照组差异无统计学意义(P0.05),女性脑出血组睾与对照组差异有统计学意义(P0.05),女性患者轻度病情组血清睾含量均较中、重度组显著升高(P0.01),女性轻度病情组雌醇/睾比值均较中、重度组低(P0.01和P0.05)。女性患者少量出血组血清睾含量均较中、大量出血组明显升高(P0.01),女性患者血清雌醇和雌醇/睾比值不同出血量组差异均无统计学意义(P0.05)。男、女性患者显著好转组雌醇含量均较无变化组及恶化组升高(P0.05~P0.01),男、女性患者显著好转组睾含量均较无变化组及恶化组下降(P0.05~P0.01),男、女性患者显著好转组雌醇/睾比值均较无变化组及恶化组升高(P0.05~P0.01)。结论:高血压脑出血患者血清雌醇、雌醇/睾比值测定有助于判断预后。
Objective:To investigate the serum levels of estradiol and testosterone in patients with hypertensive intracerebral hemorrhage and their relations with illness severity and prognosis. Methods:The serum levels of estradiol and testosterone in 168 patients with hypertensive intracerebral hemorrhage ( cerebral hemorrhage group ) and 60 healthy people ( control group ) were determined. All patients were scored by U. S. National Institutes of Health Stroke Scale, and compared in two groups. Results:The differences of the serum levels of estradiol and testosterone in male between two groups were statistically significant(P 0. 05). The serum level of estradiol in male patient with mild illness was moderate,and high in severe patients(P 0. 05). The serum levels of estradiol and testosterone in male patients with small amount of bleeding were higher than those in male patients with median amount of bleeding(P 0. 05). The difference of the estradiol serum level in female between two groups was n

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氧化硅负载Dawson型磷钨酸H6 P2 W18 O62/SiO2为催化剂,采用环己和1,2-丙醇为原料合成环己1,2-丙醇缩.探讨H6 P2 W18 O62/SiO2对缩反应的催化活性,较系统地研究了各种因素对产物收率的影响.实验表明:H6 P2 W18 O62/SiO2是合成环己1,2-丙醇缩的良好催化剂,在n(环己)∶n(1,2-丙醇)=1∶1.5,带水剂环己烷6 mL,催化剂用量占反应物料总质量的0.6%,反应时间60 min的优化条件下,环己1,2-丙醇缩的收率可达85.4%.
Cyclohexanone 1,2-propanediol ketal was synthesized from cyclohexanone and 1,2-propanediol in the presence of H6 P2 W18 O62/SiO2 as catalyst.The factors influencing the synthesis were discussed and the best reaction conditions were found out .Experimental results showed that H 6 P2 W18 O62/SiO2 was an excellent catalyst .The optimum conditions are:molar ratio of cyclohexanone to 1,2-propanediol is 1∶1.5, the volume of cyclohexane as the water-carrying agent is 6 mL, the quantity of catalyst is equal to 0.6%of feed stocks , and the reaction time is 60 min.Under these conditions , the yield of cyclohexanone 1,2-propanediol ketal can reach 85.4 %.

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建立了分散液液微萃取( dispersive liquid-liquid microextraction,DLLME )-在线衍生化-气相色谱-质谱( GC-MS)方法,将其用于环境水中6种苯甲类紫外吸收剂( BPs)(苯甲、2,4-羟基苯甲、2-羟基-4-甲氧基苯甲、4-羟基苯甲、2-羟基-4-辛氧基苯甲、2,2′-羟基-4,4′-甲氧基苯甲)的检测。系统优化了在线衍生化的条件(如进样口温度、不分流时间、衍生化试剂用量)以及 DLLME 萃取条件(如萃取剂种类、分散剂种类、萃取剂与分散剂比例、样品体积、样品溶液离子强度及 pH 值)等。在最优的条件下,所考察的6种BPs检出限为0.011~0.15μg/L,重现性( RSD)为0.7%-16.6%。该方法结果准确可靠,操作简单,富集效果好,成本较低,环境友好,在实际样品检测中具有一定的应用前景。
A method of dispersive liquid-liquid microextraction( DLLME)combined with online derivatization-gas chromatography-mass spectrometry( GC-MS)was developed for the determi-nation of benzophenone-type ultraviolet( UV)filers( BPs)in environmental aqueous samples. It is found that the online derivatization was superior to the off-line derivatization with its simplicity,high reaction efficiency and less consumption of potential poisonous reagents. The influential factors for online derivatization,including the temperature of the injection port,the splitless time,the proportion of derivatization reagent and sample solution,were initially opti-mized. In addition,the influential factors for DLLME,including the type of the extractant and dispersing solvent,the proportion of the extractant and the dispersing solvent,the volume of sample solution,the pH and the salt concentration of the sample solution were individually optimized in detail. Under the optimized derivatization and DLLME co
建立了一种利用气相色谱测定丁二酮的定量分析方法。采用FID检测器和HP-5毛细管色谱柱,对2,3-丁二酮进行定量分析。以该方法测定2,3-丁二酮的平均回收率为101.5%,标准偏差(峰面积响应值)为18.5818,变异系数为0.59%,线性决定系数(r2)为0.9999。结果表明该方法适用于2,3-丁二酮的定量分析。
To establish a quantitative determination method for analysis of 2,3-butanedione,FID detector and HP-5 capillary column were used for GC analysis. Obtained by this method,the mean recovery was 101.5% ,the standard deviation was 18.5818,the coefficient of variation was 0.59% ,the linear correlation coefficient was 0.9999. The method was suitable for quantitative determination of butanedione.

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摘要:以对叔丁基杯[4]芳烃为原料脱除叔丁基得到杯[4]芳烃,再经醚化、缩合两步反应首次合成25,27-(α,γ-二酮苯丁氧基)-26,28.羟基杯[4]芳烃,其结构经1HNMR、13CNMR、MS及元素分析表征。研究表明,目标化合物中的α,γ-二酮结构存在醇异构现象,在溶液中其醇异构体比例近似为1:2。
25,27-Di(α,γ-diketophenylbutoxy)-26,28-dihydroxy calix[4]arene was synthesized by a two-step reaction of etherifica-tion and condensation from calix [4] arene,which was prepared by p-tert-butylcalyx [4] arene as the raw material via dealkyla-tion.The structure of title compound was characterized by 1 H NMR,13 C NMR,MS and elemental analysis.The results also indicated that keto-enol tautomerism of the α,γ-diketo motif of the title compound was observed and the ratio of the keto-enol isomer approxi-mately was 1:2.

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