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The composite catalyzercan effectively catalyze cyclize reaction on the sysnthesis of N-phenyl maleimide.

合成N-苯基马来酰亚胺的最佳工艺条件为;原料摩尔配比为1;1.2;溶剂为20;1;初期反应温度为40~50℃,环化反应温度为135℃;环化时间为2h。

The third part of this thesis is reactive simulating calculation In this section, some well-known auxiliaries are selected to compute in density functional theory B3LYP on Gaussian 03, from which the relationship between reaction active energies of transition states and enantiomeric excess of chiral products homoallylic alcohols isobtained based on relative reactive ratio theory. Using this relationship, calculations on the reaction of more than eight auxiliaries with four other aldehydes are carried out in AMI and MNDO, proving that N,N\'-dibenzyl tartamide has higher enantioselectivity than others in this reaction.

第三部分为计算化学部分,运用密度泛函理论B3LYP方法在Gaussian03软件上对已经报道的几种手性配体参与的醛不对称烯丙基化反应过程进行模拟计算,基于相对反应速率理论找出两种构型过渡态间活化能的差异与产物光学收率之间的关系;并以此为基础,用AM1和MNDO方法对上述合成的几种配体控制的反应过程进行量化计算,从而在理论上证实了N-苄基酒石酸二酰胺配体在醛的不对称烯丙基化反应中具有较高的立体选择性。

In a similar way, using N,N\'-dibenzyl tartamide as auxiliary,-(2-methyl)allyl-2-chloro-phenyl-methyl azide, a vital intermediate of Repaglinide, can be prepared via asymmetric allylation of o-chlorobenzaldehyde in

产物经氧化和碘加成内酯化反应得到阿伐他汀中间体(3R,5S)-3-羟基-5-碘甲基戊内酯(10);将N-苄基酒石酸二酰胺用于邻氯苯甲醛的不对称烯丙基化反应以较高光学收率得-甲基烯丙基-2-氯苯基-甲基醇

Five kind of intermediates are synthesized with the material of p-iso-Octylphenol and Dicarboxylic acid through two different routines in.

本文以辛基酚和五种二羧酸为原料,通过酰基化反应和酯化重排反应方法,合成了五种表面活性剂中间体。

Using 2-bromo-ethanesulfonic acid sodium salt ,α,ω- binary primary amine and dodecanoic acid as the main raw materials, drawing support from two-step synthesis of experiments—Alkylated reaction and Schotten-Baumann acylation, A series of LAS(12-s-12) gemini surfactants were synthesized.

并以2-溴乙基磺酸钠、α,ω-二元伯胺、月桂酸等为主要原料,借助胺基的烷基化和Schotten-Baumann酰基化反应制备了α,ω-烷撑-双钠盐LAS(12-s-12)表面活性剂,联结基团为亚甲基—(CH2)s—(S=2,4,6,8,12),取得以下进展

Using pentaerythritol as initiator, boron trifluoride diethyl etherate as catalyst.dichloroethane as dispersion agent, the chloride polyether polyol is synthesized based on the mechanism of cationic ring-opening polymerization of epiclilnrohyclrin.The azide polyether polyol is synthesized, in DMF through A and sodium azide, and the non-reported azide energetic curing agent is synthesized through the adduction of B and IIDI.

以季戊四醇为起始剂,三氟化硼乙醚为催化剂,1,2—二氯乙烷为分散剂,环氧氯丙烷经阳离子开环聚合反应制成氯化聚醚多元醇,A在N,N—二甲基甲酰胺中与叠氮化钠反应制得叠氮聚醚多元醇,B与六亚甲基二异氰酸酯加成反应制得未见文献报道的叠氮固化剂。

A new fused polycyclic indoline compound was synthesized from aniline,with the key step of Pd-catalyzed tandem cyclization using hydroquinidine as the ligand and molecular oxygen as a green oxidant.

以芳香氨为原料,通过烯丙基化、重排、酰基化及钯催化的氧化环合反应合成了一种新的氮杂三环吲哚啉化合物,其结构经1H NMR,13C NMR,IR及HR-MS表征。

The PEI grafted on the surface of nylon was modified by the alkyl halide such as bromohexane and iodomethane,to give high-molecular-weight antimicrobial quaternary ammonium salts.

尼龙6用4-溴丁酰氯活化,再与高分子聚乙烯亚胺在有机溶剂中进行反应,使PEI共价接枝在载体上,然后用卤代烷对接枝在尼龙6上的PEI进行烷基化反应,使其形成具有杀菌功能的高分子季铵盐,制备出尼龙树脂固定化的高分子抗菌杀生剂。

The nylon was activated with organic functional groups,and after that reacted with high-molecular-weight polyethyleniminein the organic soleent. PEI was grafted covalently on the surface of nylon. The PEI grafted on the surface of nylon was modified by the alkyl halide such as bromohexane and iodomethane,to give high-molecular-weight antimicrobial quaternary ammonium salts.

摘 要:尼龙6用4-溴丁酰氯活化,再与高分子聚乙烯亚胺在有机溶剂中进行反应,使PEI共价接枝在载体上,然后用卤代烷对接枝在尼龙6上的PEI进行烷基化反应,使其形成具有杀菌功能的高分子季铵盐,制备出尼龙树脂固定化的高分子抗菌杀生剂。

By means of molecular designing, a series of sodium branched-alkyl benzene sulfonates weresynthesized through seven process, involving Frieded-Crafts reaction, Grignard reaction, sulfonationand neutralization. Those isomers have similar structure, carbons of same quantity, but the position ofalkylaryl dissimilarity. Liner fat acid, metaxylene and halogenated hydrocarbon of different carbonnumber were used as the starting materials. Optimum processing condition was confirmed consideringinfluence of a series of reaction factors such as feed proportioning, quantity of catalysts, quantitysolvent, reaction time, temperature and pressure. Eight kinds of isomers of sodium hexadecylxylolsulfonates were finally synthesized, and characterized by FT-IR.

本文通过分子设计,以不同碳数直链脂肪酸、间二甲苯以及不同碳数的卤代烷为原料,经酰基化、格氏反应、加氢还原、磺化及中和等反应,合成了结构相似、烷烃链碳数一定、芳基在烷烃链不同位置的烷基芳基磺酸盐同分异构体;并考察了原料配比、催化剂用量、反应时间、反应温度、溶剂用量、反应压力等一系列因素对各反应的影响,进而确定最佳工艺条件,最终合成出十六烷基二甲苯磺酸钠的八种同分异构体,利用 FT-IR 对产物结构进行了分析。

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