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乙酰氧基

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In this dissertation, the stable radical cation salts ofphenothiazine and 10 - alkylphenothiazine alky=〓(〓 hexachloroantimonate,perchlorate and iodide were prepared by one- electron oxidationwith 2,2,6,6-tetramethyl - 4 -acetyloxypiperidine oxoammoniumhexachloroantimonate, perchloric acid/hydrogen peroxide andmolecular iodine respectively, and they were characteried by UV -Vis spectroscopy and ESR spectroscopy.

本文的主要内容有:吩噻嗪和10-烃基吩噻嗪分别被碘、高氯酸/过氧化氢,2,2,6,6-四甲基-4-乙酰氧基哌啶氧铵六氯锑酸盐氧化为相应的正离子自由基碘盐、高氯酸盐、六氯锑酸盐,并用UV-Vis光谱和ESR波谱进行了鉴定和研究。

Amino desacetoxycephalosporanic acid (7 - ADCA) is an ampholyte.

7-氨基去乙酰氧基头孢霉烷酸是两性化合物,从等电点两侧改变溶液的 p H值都可以产生过饱和度并结晶得到晶体产品,本文对 7-ADCA两种方法结晶的初级成核过程进行了研究。

In a system consisting of 20% PEG 400 and 12% magnesium sulfate, the partition coefficient of PGA was less than 0.01, PGA almost completely partitioned into the magnesium sulfate-rich bottom phase. Meanwhile, the partition coefficient of cephalexin was 6.7, the partition coefficients of phenylglycine methyl ester and 7-ADCA were 1.5 and 1.2, respectively.

通过考察头孢氨苄、苯甘氨酸甲酯和7-氨基脱乙酰氧基头孢烷酸(7-ADCA)在ATPS中的分配行为建立了一个含20%PEG 400和12%硫酸镁的ATPS,在此体系中头孢氨苄的分配系数为6.7,苯甘氨酸甲酯的分配系数为1.5,7-ADCA的分配系数为1.2,且青霉素酰化酶的分配系数小於0.01。

He first synthesis of the precursor 45b of Tuxpanolide was accomplished fromβ-alkoxy aldehyde and β-acetoxy-γ-butyrolactone by the Aldol reaction.

uxpanolide的合成前体45b的首次不对称合成:以β-烷氧基开链醛和β-乙酰氧基-γ-丁内酯参与的Aldol醛醇缩合反应首次得到了前体化合物45b。

The first asymmetric synthesis of trans-β-hydroxy-γ-butyrolactones:-(3R, 4R, 5S)-4-(1-acetoxy-isopropyl)-3-hydroxy-butyrolactone 65a was achieved starting from isobutylaldehyde through nine steps. The key steps involve the construction of three chiral carbon centers by the Sharpless's asymmetric epoxidation and Substrate directable chemical reaction.

以异丁醛为起始原料,经过九步反应首次设计合成了具有三个手性中心的trans-β-羟基-γ-丁内酯:-(3R,4〓,5S)-4-(1-乙酰氧基-异丙基)-3-羟基-丁内酯65a,关键步骤是Sharpless不对称环氧化和底物定向不对称合成反应。

The wholly aromatic four-component copolyesters were prepared from p-acetoxy-benzoic acid, hydroquinone diacetate, 2,6-naphthalene dicarboxylic acid and isophthalic acid by melting polycondensation.

由对乙酰氧基苯甲酸、对苯二酚二乙酯、2,6-萘二甲酸及间苯二甲酸四种单体通过熔融缩聚反应,合成了全芳香族四组分共聚酯。

Deoxybenzoin(3) was prepareded by using the resorcinol and substituted phenylacetic as starting meterials in microwave-mediated.Then the compound(3) was reacted with acetic anhydride to produce(4).The compound(4) was hydrolyzed to convert compound(5) in the acid-mediated. The compound(5) was reacted with the 1,2-dibromo-ethane and 1,3-dibromo-propane in refluxed condition with acetone as solvent to give(6) or(7),respectively.Lastly,the title compounds were synthesized by refluxing(6) or(7) with 2-methyl-benzimidazole and potassium carbonate in acetone solution.

以取代苯乙酸和间苯二酚为起始原料,用微波辐射法合成脱氧安息香(3),(3)与乙酸酐缩合生成2-甲基-7-乙酰氧基异黄酮(4),(4)在酸性条件下水解生成相应的异黄酮(5),化合物(5)分别与1,2-二溴乙烷和1,3-二溴丙烷反应生成(6)和(7),化合物(6)和(7)再分别与2-甲基苯并咪唑偶合生成目标化合物。

In thesecond chapter, eleven 1,3,4-oxadizoles bearing chiral pyrazolyl moieties(4a-k) andfive triazolotriazines bearing chiral pyrazolyl moieties(5a-e) were obtained from5-[(1"S)-1",2-diacetyl-oxyethyl]-1-phenylpyrazol-3-carboxaldehyde(1) with arylcar-bohydrazide or (5-aryl-1,2,4-triazin-3-yl)hydrazine through an intramolecular1,3-dipolar cycloaddition in the presence of the non-metal oxidant IBD.

其中第二章介绍了以D-葡萄糖为原料制得的5-[(1′S)-1′,2′-二乙酰氧基乙基]-1-苯基吡唑-3-醛(1)分别与芳基甲酰肼、(5-取代苯基-1,2,4-三嗪-3-基)肼反应,在无金属氧化剂—IBD引发下,发生分子内1,3-偶极环加成,采用&一锅煮&法合成了11种含手性吡唑基的1,3,4-噁二唑类化合物(4a-k)和5种含手性吡唑基的三唑并三嗪类化合物(5a-e)。

Phenothiazines were also oxidized byiodine and 2, 2, 6, 6- tetramethyl - 4 - acetyloxypiperidineoxoammonium hexachloroantimonate to radical cations in the cavityof β-cyclodextrins in aqueous solution.

以吩噻嗪衍生物为底物,2,2,6,6-四甲基-4-乙酰氧基哌啶氧铵六氯锑酸盐、碘为氧化剂,二者在水相中β-环糊精腔内发生了单电子转移反应,产生了吩噻嗪衍生物正离子自由基。

Finally, we discuss the preparation, characterization and application of alkylsilane and mercaptoacetoxy monolayers on ordered mesoporous titanosilicate molecular sieve.

最后,我们讨论了介孔钛硅分子筛表面烷基硅烷单层和巯基乙酰氧基单层的制备、表征及应用。

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