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Functionalized propargylic dithioacetals have been applied to one-pot furan annulation to afford the corresponding functionalized oligoaryls.

中文摘要应用官能基化的炔丙基硫缩酮进行一锅式呋喃稠合反应,可产生相对应之寡联芳香环化合物。

METHODS 3-methoxy-7α-methylestra-1,3,5(10)-trien-17β-ol was reducted with lithium and ammonia,then the intermediate was hydrolyzed in oxalic acid and reacted with malonic acid to get 3,3-dimethoxo-7α-methylestra-5(10)-en-17-ol(compound 4),which was oxidated by pyridium bichromate ,reacted with acetylene,and hydrolyzed in oxalic acid again to get the product tibolone.

方法以3-甲氧基-7α-甲基雌甾-1,3,5(10)-三烯-17β-羟基为起始原料经锂胺还原、草酸水解、缩酮化得3,3-二甲氧基-7α-甲基雌甾-5(10)-烯-17β-羟基(化合物4),然后用温和的氧化剂重铬酸吡啶盐氧化、炔化、再水解得目的产物。

At the meantime, we synthesized the chiral spiroketal enol ether steroselectively and their absolute configuration were determined.

我们还对螺环缩酮烯醇醚类化合物的立体选择性形成规律进行了探索,并取得了积极的结果。

Systematic studies on the Hetero-Diels-Alder reaction between the o-Quinone methidesand different enol ether dienophiles for the construction of the spiroketal skeleton was described.

较系统地研究了邻甲基苯醌与不同的烯醇醚亲双烯体之间的Hetero-Diels-Alder反应对螺环缩酮结构的构筑及其应用。

A novel carbonyl transposition led by anilines'nucleophilic addition to methyl 2-keto α-D-glucopyranoside was discovered. And the mechanism of the reaction concerned to an enol rearrangment was provided through tracing the change of 〓H-NMR and 〓C-NMR of a hemiacetal intermediate which was obtained in the reaction of o-phenylene diamine with 2-keto glycoside. Both the intermediate and the converting product were identified by 〓H-NMR,〓C-NMR,〓H-〓H COSY and HMQC.

一、发现了2-位氧化α-甲基D-葡萄糖苷的芳胺亲核加成引起羰基转位的新方法,利用核磁共振氢谱及碳谱对邻苯二胺与2-位氧化α-甲基D-葡萄糖苷加成生成的稳定中间体半缩酮化合物在氘代丙酮中的变化进行跟踪,结合对转化产物的氢氢相关谱和HMQC结构确证,提出了该反应中2-位羰基通过烯醇化互变而转至3-位的机理并得到了验证。

The main impurity involved in the synthesis of erythromycin oxime was separated and purified, which was identified as the very compound formed in the acidic hydrolysis of erythromycin A, i.

分离和鉴定了在合成红霉素肟的过程中产生的一种主要杂质,通过 IR,UV,MS,1 H NMR和 1 3C NMR确证它和红霉素在酸性水解时生成的红霉素 A 8,9-脱水- 6,9-半缩酮为同一化合物。

In ethylene glycol solution, 1 was converted into 1-oxo-13c-(2-hydroxyethoxy)-1, 13c-dihydro-dibenzo -xanthene (23) and ketal compound 7a, 13bethylenedioxy-1-hydroxy-7a, 13b-dihydro-dibenzo -xanthene (24), the structure of which was confirmed by X-ray single crystal diffraction.

在乙二醇中反应时,1被氧化为二苯并咕吨型的23和缩酮型的7a,13b-亚乙二氧-1-羟基-7a,13b-二氢-二苯并-咕吨(24)。24的结构得到X-ray单晶衍射的证实。

The last part is concerning the new application of dialkyl-substituted propargylic dithioacetals.

第三部分则是双烷基取代炔丙基硫缩酮的新型态反应。

The beta-thioalkoxyalcohols could be obtained in good yields by the reaction of dialkyl-substituted propargylic dithioacetals with a series of carbonyl compounds.

我们发现在铁触媒和格林那试剂的存在下,利用双烷基取代炔丙基硫缩酮和羰基化合物反应生成的beta-硫烷氧基醇,可以进行不常见的beta-氧消去反应,而得到烯炔衍生物。

However, alkyl-substituted propargylic dithioacetals could be synthesized by the displacement reaction of the corresponding terminal alkynes with alkyl iodides.

烷基取代的炔丙基硫缩酮衍生物,则能利用相对应的末端炔和碘烷亲电基进行取代反应所获得。

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客人们在卡罗利娜·埃凯家里,举止就文雅一些,因为卡罗利娜的母亲治家很严厉。

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