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甲缩醛

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We have had the extensive studies on theα-acetyl-α-carbamoyl ketene--acetals and its further applications, for example, their adols condensations with aldehydes giveα-alkenoyl-α-carbamoyl ketene--acetals which can be utilized as the 1,5-bielectronic five-carbon components to react with various binucleophlilic species in a [5+1] annulation.

我们小组在以前的工作中对α-乙酰基-α-胺甲酰基二硫缩烯酮在合成中的应用进行了深入的研究,如与醛缩合生成α-烯酰基-α-胺甲酰基二硫缩烯酮,将其作为1,5-双亲电五碳合成子的[5+1]成环策略等。

Result s:10 μmol/L retinoids could inhibit the Bel-7402 proliferation and decrease the colony forming of liver cancer cells on soft agar significantly.So some biochemical markers indicating the proliferation status of liver cancer cells changed significant ly, including the significant activity increase of ornithine carbamyl transferase, tyrosine-α-ketoglutaric transaminase and alkaline phosphatase, the significant decrease α-fetoprotein secretion,γ-glutamyltranspetidase and aldolase activity.

结果:10μmol/L维甲酸显著抑制肝癌细胞增殖,并使肝癌细胞软琼脂集落形成率明显减少,使代表肝细胞分化的酶鸟氨酸氨基甲酰转移酶、酪氨酸-α-酮戊二酸转氨酶和碱性磷酸酶比活力明显升高,甲胎蛋白分泌量、γ-谷氨酰转肽酶和醛缩酶比活力明显下降。

In this paper, Claisen condensation of isochroman ?4?one as starting material with diethyl oxalate is carried out to form β?diketone compound of isochroman ?4?one.

以异色满酮 4为起始原料,经Claisen缩合得其β二酮衍生物,再与水合肼进行Knorr反应环合成 3 乙氧甲酰基和 3 肼甲酰基异色满并吡唑衍生物,通过酰肼与糠醛反应成腙后,分别与巯基乙酸和氯乙酰氯反应合成了标题化合物

The acetalization and ketalization of various aldehydes and ketones with catechol by using HY zeolite as catalyst were studied.

研究了 HY分子筛催化邻苯二酚与环己酮、丁酮、丙酮、丙醛、丁醛、异丁醛、戊醛、异戊醛、正己醛、正辛醛、苯甲醛、二苯甲酮等十余种醛的缩合反应。

The acetalization and ketalization of various aldehydes and ketones with glycerol by using KHSO4 as catalyst were studied. Effect of reaction time, mole ratio of reactants and amount of catalyst on yield of acetals were investigated.

研究了在KHSO4催化下,丙三醇与环己酮、丁酮、丙酮、丙醛、丁醛、异丁醛、戊醛、异戊醛、正辛醛、二苯甲酮、苯甲醛等十余种醛的缩合反应。

The acetalization and ketalization of various aldehydes and ketones with glycols using FeCl3 as catalyst were studied. The effects of reaction time, mole ratio of reactants and amount of catalyst on the yield of acetals were investigated.

研究了在FeCl3催化下,乙二醇与环己酮、丁酮、丙酮、丙醛、丁醛、异丁醛、戊醛、异戊醛、正辛醛、二苯甲酮、苯甲醛等十余种醛的缩合反应。

Starting with two reactive methylene compounds, ethyl cyanoacetate and malononitrile, two 5-amino-1H-pyrazoles were prepared through the intermediates ketene dithioacetal.

从两个活泼亚甲基化合物开始,经过乙烯酮二硫代缩醛中间体,合成了两个5-氨基-1H-吡唑,以这个两个化合物为中间体,与芳香族和脂肪族α-溴代酮反应,而后经酸催化亚胺化互变异构后得到含咪唑并[1,2-b]吡唑甲硫醚类化合物6a-6g。

Bis-imidazoline was prepared from triethylene tetraamine and N,N-dimethylformamide dimethyl acetal at 85℃ for 2 h with toluene as solvent, with a yield of 90.4%. The reaction of bis-imidazoline with 1,2-dibromoethane and potassium carbonate in acetonitrile provided with a monobromide salt yield of 78.7%. Hydrolysis of monobromide salt under aqueous causic solution formed 1,4,7,10-tetraazzcyclododecane in a 74.2% yield.

用甲苯作溶剂,使三乙烯四胺和N,N-二甲基甲酰胺二甲基缩醛在85℃反应2 h,得到中间体双咪唑啉,产率90.4%,在乙腈溶剂中,碳酸钾存在下,双咪唑啉和1,2-二溴乙烷进行扩环反应,得到环状中间体一溴盐,产率78.7%,一溴盐经碱性水解2 h,得到1,4,7,10-四氮杂十二烷,产率74.2%。

Aldol condensation 2, 5-dimethoxymethoxyacetophone with 2, 4, 6 -tri methoxymethoxybenzendehyde, then hydrogenation, reductive, the key intermediate 83 (84) of natural product 3, 5, 7, 2′, 5′- pentahydroxyflavan, was obtained; Mini reviewed EGCg activity, Then gallic acid and phloroglucin were used to synthsis EGCg, The key intermediate Chalcone 109 of EGCg was abtained through 7 steps from gallic acid.

重点介绍了以没食子酸为原料,经酯化,保护,还原,氧化,格氏反应,氧化六步反应得到3,4,5-三苄氧基苯乙酮,以间苯三酚为原料,经维斯迈尔反应,苄基保护,甲氧甲氧基保护三步反应得到2,4-二苄氧基-6甲氧甲氧基苯甲醛,酮106与醛108经羟醛缩合得到EGCg重要反应中间体查尔酮109。

The intermediate 5-amino-1H-pyrazole-4-carboxylic acid ethyl ester prepared in the first part underwent successively hydrazinolysis, condensations with ketene dithioacetals and alkylations to give rise to the dipyrazolyhnethanes.

从第一部分中的中间体5-氨基-1H-吡唑-4-羧酸乙酯开始,经过肼解、与乙烯酮二硫代缩醛的缩合反应和烷基化反应,合成了二吡唑基甲酮类化合物。

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This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

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