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酰化

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Three new fulvene polymeric compounds, namely 1[Ag (L3]CH2C12 , 2[Ag2(L25(H2O)(S03CF3)2]0.5C6H6 and 3 Mn(L42(C2H5OH)2 , were synthesized, respectively. Compounds 1 and 2 reported herein represent the organometallic polymers based on both Ag-N and Ag-C coordination interactions. In the solid state, compound 3 are bound together by strong intermolecular N H-O hydrogen bonding system into a supramolecular one-dimensional H-bonded chain.B.

一、富烯有机配体的合成及与金属离子的反应化学利用富烯负离子的芳酰化反应和Heck-偶联反应合成了富烯配体L1-L18,并合成了三个基于富烯配体的金属有机配位聚合物1[Ag(L3]·CH_2Cl_2、2[Ag_2(L25(H_2O)(SO_3CF_3)_2]·0.5C_6H_6和氢键驱动的超分子聚集体3Mn(L4_2(C_2H_5OH)_2。

METHODS:This compound was synthesized via acylation and hydrogenization using aciclovir and CBZ-L-valine as meterial.

以阿昔洛韦和N-苄氧羰基-L-缬氨酸为原料,经酰化、催化氢解反应得到了新型抗疱疹病毒药物缬昔洛韦。

Pharmacological results also indicated that the carbonyl and imino of Z-47 are important to its marked antiinflammatory and analgesic activity. The activity will be reduced or abolished with Z-47 converted to oximes or/and acetamides.

药理结果还表明,Z-47结构中的羰基和仲胺基对Z-47的显著抗炎镇痛作用具有重要的贡献,将Z-47羰基变成肟或/和将Z-47仲胺基酰化都会造成抗炎镇痛作用的降低甚至是丧失。

The first synthetic route uses 1,2,4-trimethoxybenzene and chloroacetonitrile in forming 2,4,5-trimethoxy-a-chlor-acetophenone under the anhydrous condition, then the intermediate condensates with papaverine forming the core pyrro[2,l-a]isoquinoline, followed by formation and lactonization to form the lactone ring. The second synthetic route uses prepared aldehyde with prepared ethyl nitroacetate by Knoevenagel condensation to obtain 2-Nitro-3-(2,4,5-tris-methoxy-phenyl)-acrylic acid ethyl ester and 2-Nitro-3-(2,4,5-tris-benzyloxy -phenyl)-acrylic acid ethyl ester etal intermediates. The lamellarin skeleton could arise from condensation of the papaverine and these intermediates by Michael reaction, the ester group is provided for subsequent lactonization. The third synthetic route uses coumarin or indan-l,3-dione derivatives and papaverine to form lamellarin under basic conditions.

第一条路线首先从1,2,4-三甲氧基苯出发与卤乙腈作用合成卤代芳酮中间体,然后与罂粟碱反应合成开链片螺素,最后经乙酰化、去保护、成内酯环得到片螺素;第二条路线由制备的芳醛和制备的硝基乙酸乙酯经缩合得到2-硝基-3-芳基丙烯酸乙酯,然后由该中间体与罂粟碱反应,在完成关环的同时也引入酯基,最后去保护、成内酯环得到片螺素;第三条路线是由香豆素或茚二酮出发,经溴代后的中间体与罂粟碱反应,得到片螺素的基本框架。

The solubility in general organic solvents, oleic acid and lipin of both derivatives were also studied. In order to find out the solubilities in general organic solvents, PhCS that had satisfied solubility in DMF, DMAC and DMSO and EHCS that was amphiphilic were prepared.

为考察壳聚糖衍生物在通用有机溶剂中溶解性问题,我们制备出了在DMF、DMAC、DMSO等通用有机溶剂中溶解性很好的邻苯二甲酰化壳聚糖以及水油两亲性的乙醚胺壳聚糖。

The dependence of the relative intensity of cationic molecule and fragmentation ion of an acetylated melezitose on the concentration of Na + or Li + in the matrix was studied by using fast atom bombardment source .

利用快原子轰击源研究了乙酰化松三糖的阳离子化分子和碎片离子的相对强度随底物中Na+或Li+浓度变化的趋势。

We ever reported cellulose is in propyl of Xi of ionic liquid 1-- chloric salt of Zun of 3- methylic Mi (the homogeneous phase acetyl in Am ImC L) converts reaction, falling without activator condition, one pace gets the CA of different DS, get acetone but the CDA[12] of dissolve.

我们曾报道了纤维素在离子液体1-烯丙基-3-甲基咪唑氯盐中的均相乙酰化反应,在无催化剂条件下,一步得到不同DS的CA,并得到丙酮可溶的CDA[12]。

The antioxidant activity of the lipid-soluble epigallocatechin-3-O-gallate-4'- myristate in soybean salad oil were investigated and compared in AOM t.

通过酰化反应得到EGCG肉豆蔻酸酯,利用高速逆流色谱对反应产物进行分离和纯化,并进行了元素分析、MS和1H-NMR等表征,同时用活性氧法考察了其在大豆色拉油中的抗氧化活性。

Methods HP-1 cells were induced into macrophages by phorbol myristate acetate, and were treated with acetylated low-density lipoprotein to establish the THP-1 macrophage derived foam cell models.

佛波酯刺激THP-1细胞分化为巨噬细胞后经乙酰化低密度脂蛋白诱导泡沫化,建立THP-1巨噬细胞源性泡沫细胞模型。

The reaction of inulin with octadecyl isocyanates resulted in carbamoylated inulins from which the interfacial properties were determined.

菊糖与十八烷基异氰酸酯在有机溶剂中发生甲氨酰化反应,生成的氨甲基菊糖具有表面活性。

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