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甘氨酸

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This new zinc source is a zinc gluconate stabilized with glycine.

这种新的锌来源是用甘氨酸稳定的葡萄糖酸锌。

Enzymatic synthesis of cefaclor from 7\|aminodesacetoxymethyl\|3\|chlorocephalosporanic acid (7\|ACCA) and phenylglycine derivatives using penicillin G acylase was studied.

以7-氨基去乙酰氧甲基-3-氯头孢烷酸(7-ACCA)和苯甘氨酸衍生物为底物,利用青霉素酰化酶酶促合成头孢克罗。

Moreover, D-sodium gluconate was mixed with other substances and used as corrosion inhibiting admixtures. The admixture of D-sodium gluconate and sodium tetraborate has the best inhibiting effect among these mixed inhibitors.

复配试验表明,D—葡萄糖酸钠与四硼酸钠组成的复合缓蚀剂缓蚀效果最好,而与甘氨酸和乙醇胺复配的缓蚀剂也表现出较好的缓蚀效果。

Compound 4 is a lanthanide-polyoxometalate wavelike chain, with racemic proline molecules situated in the framework via hydrogen bonds.

化合物5显示B型Anderson多酸与稀土-甘氨酸配合物形成的3D超分子孔道结构。

Three powders were used: adipic acid, microcrystalline cellulose, and glycine.

3粉使用:己二酸、微晶纤维素、甘氨酸

Objective: To study the effects of PKC inhibitor chelerythrine on the releases of GABA and Gly from ischemic rat striatums.

目的:研究蛋白激酶C抑制剂Chelerythrine对大鼠脑缺血时纹体γ-氨基丁酸和甘氨酸释放的影响。

It was found that the more easily systhesized and stable N, N-acetal or N, Ohemiacetal can replace N-tosyl imino ester to react with phenols in the presence of TiCl〓, and α-arylglycine derivatives were also obtained in high yields and high regioselectivity.

进一步研究发现,更易合成的N,N-或N,O-缩醛可以作为亚胺酯的替代物和酚类化合物发生傅克反应。路易酸TiCl〓能有效地促进酚类化合物和亚胺酯的傅克反应较高产率、较高区域选择性的得到2-羟基α-芳香甘氨酸衍生物。

In the forth part, in the presence of chiral phosphoric acid, highly enantio-enriched (up to 98% ee)α-aryl glycine derivatives could be synthesized via asymmetric transfer hydrogenation of the α-aryl imino esters using Hantzsch ester as the hydrogen source.

第四部分工作中,利用Hantzsch酯作为氢源,高对映选择性地实现了手性磷酸催化芳基酮酸酯亚胺的不对称仿生氢化反应,以最高98%的对映选择性得到苯甘氨酸衍生物。

Mehods Commercially available glycine ethyl ester hydrochloride was used as starting material to give the target compound via addition, protection with BOC, Dieckmann cyclation, reduction with NaBH4 and LiAlH4, protection, oxidation, oximation and deprotection.

甘氨酸乙酯盐酸盐为原料,依次经加成、BOC保护氨基、Dieckmann环化、NaBH4还原羰基、LiAlH4还原氰基、BOC保护氨甲基、氧化、肟化、脱BOC保护等9步反应制得目标化合物。

Ammonium carbamate was found to be the best ammonia donor for the reaction and its favorable concentration is 120~160 mmolL^(-1). The optimal water activity, reaction temperature, pH value and concentration of D, L-HPGME are 0.55~0.75, 35~40℃, 7.5~8.0 and 40 mmolL^(-1), respectively.

该反应的最适氨源为氨基甲酸铵,其较佳浓度为120~160mmolL^(-1);最适水活度、反应温度、pH值、对羟基苯甘氨酸甲酯浓度分别为0.55~0.75、35~40℃、7.5~8.0和40mmlL^(-1)。

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