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pyrazole相关的网络例句

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Pyrazole is a kind of heterocycle compound which possesses very high activity.

吡唑作为一种重要的杂环化合物,具有很高的生物活性。

To discover new strobilurin analogues with high pesticidal activity, a series of new strobilurin derivatives containing substituted pyrazole and pyrimide ring, which included 124 novel compounds (73 compounds containing substituted pyrazole ring and 51 compounds containing substituted pyrimide ring) were designed and synthesized. In addition, 36 new intermediates were synthesized. Their structures were characterized by ~1H NMR and elemental analysis, partial compounds were characterized by MS and IR once again.

为了发现具有更好生物活性的新型Strobilurin类化合物,本论文在详尽总结文献的基础上,设计并合成了含吡唑和嘧啶环的新型Strobilurin类化合物124个,其中含吡唑环的新型Strobilurin类化合物73个,含嘧啶环的新型Strobilurin类化合物51个;未见文献报道的中间体36个,所合成的化合物经过~1H NMR、IR、LC-MS或元素分析等确定了结构。

To discover new strobilurin analogues with high pesticidal activity, a series of new strobilurin derivatives containing substituted pyrazole and pyrimide ring, which included 124 novel compounds (73 compounds containing substituted pyrazole ring and 51 compounds containing substituted pyrimide ring) were designed and synthesized. In addition, 36 new intermediates were synthesized. Their structures were characterized by 1H NMR and elemental analysis, partial compounds were characterized by MS and IR once again.

为了发现具有更好生物活性的新型Strobilurin类化合物,本论文在详尽总结文献的基础上,设计并合成了含吡唑和嘧啶环的新型Strobilurin类化合物124个,其中含吡唑环的新加热管型Strobilurin类化合物73个,含嘧啶环的新型Strob 加热管 ilurin类化合物51个;未见文献报道的中间体36个,所合成的化合物经过1H NMR、IR、LC-MS或元素分析等确定了结构。

The famciclovir was synthesized from purine by a series of steps by Acylation, Decarboxylation, Reduction ,and so on; Derivatives of these intermediates is described from the 6-chloro- 9H- purin-2-amine as raw materials in different conditions when the iodine and bromide were synthesized with the addition of two intermediate 6-bromo-9H-purin-2-amine and 6-iodo-9H-purin-2-amine; There is elaborated from the main part of a acetophenone, urineaminohydrochloride, phenylhydrazine, ethyl acetoacetate as raw material through a series of reactions to synthetic 3-phenyl-4-formylphenyl pyrazole and 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-aldehyde two pyrazole aldehyde, and then with 2-amino-6-chlorine-9-(2-methicillin-oxo-co-methyl-4-yl) purine reaction of the two new pyrazole purine Schiff bases.

本论文主是采用以鸟嘌呤为原料,经过一系列的酰基化,脱羧,还原等反应作用下最终得到了产物2-氨基-9-(4-乙酰氧基-3-乙酰氧基甲基丁基)嘌呤;其中的中间体衍生物主要是阐述从以2-氨基-6-氯鸟嘌呤为原料通过在不同的条件下进行溴代与碘代分别合成了另外两种中间体2-氨基-6-溴鸟嘌呤及2-氨基-6-碘鸟嘌呤;还有一部分主要是阐述从以苯乙酮,盐酸氨基脲,苯肼,乙酰乙酸乙酯为原料通过一系列的反应先合成3-苯基-4-醛基吡唑及5-氯-3-甲基-1-苯基-1H-吡唑-4-甲醛这两个吡唑醛,然后再与2-氨基-6-氯-9-(2-甲氧羰基丁酸甲酯-4-基)嘌呤反应得到了两个新型的吡唑嘌呤席夫碱

There was not few report about 5-amino-3-cyan-N-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole in the domestic , so that the whole synthetic course of 5-amino-3-cyan-N-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole was studied and the intermediate with feasible eco...

因此,研究5-氨基-3-氰基-N-(2,6-氯-4-三氟甲基苯基)吡唑的合成,探索其中间体经济可行的合成路线,具有很好的社会效益和经济前景。

However, three isomers are obtained when [3(5)-〓-5(3)-MeS]pyrazole or[3(5)--5(3)-MeS]pyrazole reacts with 〓 in the same conditionpossibly owing to the influence of both the steric and electronic factors.

通过配体与〓的光化学反应,首次分离得到了不对称取代的双吡唑烷VIB金属配合物,但3位取代基的立体位阻减弱了双吡唑烷与〓的反应。

Chapter III We try to synthesizing pyrazole by hydrazine and thiourea in alkaline conditions, we found we can not get the acyl pyrazole in the conditions of synthesizing succinylthydrazine and ferrocenyl chalcone, pyrazole was got instead.

第三章我们尝试以酰肼及氨基硫脲作为氮源在碱性条件下来合成吡唑类化合物,并取得了理想的结果。

The results show thatthe substitutions containing sulfur atom in the pyrazole ring remarkably affectthe steric and electronic properties of the pyrazole ligands.

因此,我们研究了吡唑环上带上S原子取代基对形成双吡唑烷配体及其与VIB金属羰基配合物的光化学反应的影响。

05Mol/L NaHCO_3 in the presence of pyrazole and the synergetic effect of pyrazole with BTA and MBT were studied using cyclic voltammetry techniques and rotating disc electrode.

利用循环伏安法和旋转圆盘电极研究了NaHCO3溶液中吡唑对紫铜的缓蚀作用,并对其与BTA,MBT之间的协同效应进行了初探。

In order to find new pyrazole leading compounds, 14 1--4-(pyrazol- 5-ylcarbony)semicarbazide devivatives were synthesized from 4-chloro-3-ethyl-1-methyl-5-pyrazole car-bonydrazide and substituted phenylisocyanate.

为了寻求新的吡唑先导化合物,用4-氯-1-甲基-3-乙基-5-吡唑甲酰肼与取代苯基异氰酸酯反应得到了14个新的1-吡唑酰基-4-芳基氨基脲类化合物。

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