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Two colorimetric anions sensors based pyrrolic amide and nitro phenyl have been synthesized in the third part.

在第三部分中,我们设计合成了两种基于吡咯酰胺和硝基苯单元的比色阴离子识别主体。

The solid-liquid reaction method was used for the preparation of HPLC aryl-bonded silica gel stationary phases, including 3, 5-dinitrobenzyl, quinolinyl ether and 1, 1'-di(2-naphthol) ether bonded silica gel stationary phases by using N-(β-aminoethy1)-γ-aminopropylmethyldimethoxy silane and 3-glyci-doxypropyl trimethoxylsilane as coupling reagents, respectively.

采用固液相连续反应,以N--γ-氨丙基甲基二甲氧基硅烷和γ-丙基三甲氧基硅烷为偶联剂,分别制备了二硝基苯甲酰胺基、喹啉醚基和联萘酚醚基三种芳基键合硅胶固定相。

The packing arrangements in their mesophases of the polymers were influenced by the end functional group obviously. All the polymers with amide-substituted group showed the partly interdigitated bilayer smectic phase structure.

另外,聚合物的热行为和相转变行为受液晶聚合物的末端键接基团影响显著,所有末端包含酰胺基团的侧链偶氮苯聚合物在液晶温度均形成了部分穿插的双层近晶相结构。

The negatively charged sulfonic acid groups was readily introduced through the reaction of the terminal anhydride groups of the anhydride-terminated hyperbranched poly precursor with the amino groups of sulfanilic acid before chemical imidization.

研究表明,在聚合过程的聚酰胺酸阶段,采用过量的邻苯二甲酸酐或苯胺对超支化聚酰亚胺的端氨基或端酸酐基团进行的封端改性切实可行,改性反应可进行地相当彻底。

Results Eleven compounds were obtained and identified as sarcodonin A, scabronine B, 3β-hydroxy-5α, 8a-epidioxyergosta-6, 22-dien,(22E, 24R)-ergosta-7, 22-diene-3β, 5α, 6β-triol,(22E, 24R)-ergosta-7, 22-diene-3β-ol, benzoic acid, 4-hydroxylben-zaldehyde, 4-monopropanoylbenzenediol, ethy1-β-D-glucopyranoside, thioacetic anhydride,(2S, 2'R, 3S, 4R)-2-(2-hydroxyoctadecanoylamino) docosane-1, 3, 4-triol.

结果共分离鉴定了11个化合物,分别是:sarcodonin A、scabronine B、3β羟-5α,5α-过氧麦角甾-6,22-二烯-3β-醇、(22E,24R)-麦角甾-7,22-二烯-3β,5α,6β三醇、(22E,24R)-麦角甾-7,22-二烯-3β-醇、苯甲酸、对羟基苯甲醛、对羟基苯甲酸乙酯、乙基-β-D-吡喃葡萄糖苷、硫代乙酸酐、(25,2'R,3S,4R)-2-(2-羟基-十八碳酰胺)二十二碳烷-l,3,4-三醇。

EVA/LDPE/ CB conductive foam was made of EVA and LDPE as matrix,HG-1P CB and ACET CB as conductive filler,AC as foamer and DCP as crosslinker.

文章以乙烯-乙酸乙烯酯和低密度聚乙烯为主基体,特导炭黑(HG-1P)和乙炔炭黑为导电填料,偶氮二甲酰胺为发泡剂,过氧化二异丙苯为交联剂,制备了EVA/LDPE/炭黑导电泡沫复合材料。

Objective To modify the synthesis of Benzhydryl 2α- methyl - 2β- [ ( 1,2,3 -triazol - 1 - yl)- methyl ] penicillanate - 1,1 - dioxide, the key intermediate of β- lactamase in-hibitor tazobactam.

目的 改进β-内酰胺酶抑制剂泰唑巴坦关键中间体2α-甲基-2β[(1,2,3-三唑-1-基)-甲基]青霉烷酸砜二苯甲酯的合成。

N-Benzylacryl amide was synthesized using acrylonitrile and benzyl alcohol as raw materials and sulfuric acid as catalyst.

以丙烯腈和苯甲醇为原料,浓硫酸作催化剂,合成了N-苄基丙烯酰胺。

Using phenol and benzyl chloride as raw materials and N,N-dimethyl formamide as solvent, benzyl phenyl ether was synthesized under microwave radiation.

采用微波辐射技术,以苯酚、氢氧化钾和氯化苄为原料,N,N-二甲基甲酰胺为溶剂合成了苄苯醚。

Then we completed the first total synthesis of-Plakoridine A using Eschenmoser couping reaction as akey step. During the synthesis we found the choice of protecting groups and the configuration of the chiralcenter of the substrate play an important role to the key Eschenmoser reaction,so we think our successwould be of guide for synthesizing other polysubstituted pyrrolidines or piperidines.

在论文的第一章中,我们先以易得的对羟基苯乙酸乙酯为原料经多步反应制得了所需的β氨基酸酯,然后利用立体选择性的Aldol缩合反应和内酰胺化反应制得了Plakoridine Alactam,随后,以Eshenmoser缩合反应为关键步骤完成了生物碱-Plakoridine A的首次不对称全合成。

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