汽车尾气中能检测到所有的目标化合物。
All the target compounds were detected in the vehicular exhaust.
对所合成的目标化合物进行了生物测定。
The insecticidal activity of all target compounds was evaluated.
结果得到目标化合物，精品收率达60%以上。
RESULTS The target compound was obtained and purified yield was over 60%.
各中间体和目标化合物结构经1HNMR确证。
The structures of all intermediates and the target compound were confirmed by 1HNMR.
用元素分析和1HNMR对目标化合物进行了表征。
The target compound was characterized by elementary analyses and 1HNMR spectra.
对中间体及目标化合物的结构及物理性质作了表征。
The structure and physical properties of intermediates and target compounds were reported.
通过1HNMR表征确定了目标化合物的结构。
我们共设计合成得到了两大类，四系列目标化合物。
One class of compounds is composed of three series of novel compounds as hybrids of podophyllotoxin with different types of isoquinolines.
采用二倍稀释法对目标化合物的体外抗真菌活性进行测试。
The antifungal activity of the target compounds in vitro was measured by consecutive double dilution.
结果提供了参考进一步的目标化合物的有机光电器件中的应用。
The results give a reference to further application to organic optoelectronic device of the target compound.
方法用p,O双齿螯合钯配合物催化偶联反应合成目标化合物。
METHODS the target compound was synthesized from cross-coupling reaction catalyzed by p, o chelate palladium complex.
目标化合物及各中间体的结构采用1HNMR和MS进行了确定。
The structures of the intermediates and the target compound were confirmed by 1H NMR and MS.
结果合成的目标化合物经1HNMR和ESI-MS确证其结构。
Results The synthesized compounds were confirmed correct by 1HNMR and ESI-MS.
所述合成反应的反应条件非常温和，可以以较高产率得到目标化合物。
The reaction conditions of the synthesis reaction are very mild, and target compounds can be obtained with higher yield.
抗真菌活性实验结果表明，目标化合物对大部分供试真菌具有好的活性。
The result of antifungal activity indicated that the target compounds had good antifungal effects on most tested fungi.
结果总收率达95.4%，目标化合物的结构经红外光谱和元素分析确证。
RESULTS the overall yield was 95.4%, the title compound was characterized by IR and elemental analysis.
方法：以丙二酸和对甲酚为原料合成目标化合物，用正交试验摸索最优条件。
Methods: the title compounds were synthesized from malonate and p-cresol. Orthogonal test was carried out to find out the optimal condition.
方法：以芦丁为原料，经苯甲酰化，水解，糖苷缩合和脱保护合成目标化合物。
Methods: Rutin was utilized as the starting material. The target compounds were produced via benzoylation, hydrolysis, glycosidation and deproteination.
对产物进行了核磁及元素分析表征，确认其结构即为目标化合物5-氟吲哚酮。
The products were characterized by means of nuclear magnetic resonance and element analysis and the structure were affirmed to accord with 5-Fluorooxindole.
采用四氢呋喃溶解聚氯乙烯、热甲苯溶解聚乙烯材料以提取样品中的目标化合物；
The target compounds were extracted with polyvinyl chloride materials dissolved in tetrahydrofuran or polyethylene materials dissolved in hot toluene.
讨论了红外吸收特征峰对应官能团的振动形式，样品的官能团与目标化合物一致。
The vibrations of the functional groups of the compound were discussed as to their homologous infrared absorption characteristic peaks.
选择了较好的一种方法合成了一系列的目标化合物以期找到具有生物活性的新型化合物。
The better process was chosen to prepare a series of the target compound in order to find novel bio-active compounds.
对目标化合物的结构进行了元素分析和光谱分析，并初步测试了目标化合物的抑菌和杀菌效果。
The structure of the product was confirmed by elementary analysis and spectrum analysis, the bacteriostatic and bactericidal effect of sample on different bacteria and germs was tested.
以2,6 -二氯吡啶为原料，通过硝化，取代，还原，环化，氧化等几步反应可得到目标化合物。
From 2, 6-dichloropyridine as starting material, we can get the target molecule through nitration, substitution, reduction, cyclization, oxidation etc.
本文中第四章解决了目标化合物(R,P) - 35和(R, P) - 36的设计与合成。
The fourth chapter of this thesis describe the synthesis of target the compounds (r, p) -35 and (r, p) -36.
方法以薯蓣皂素为起始原料，采用逐步糖苷化策略，经10步反应制得目标化合物，总收率约为15%。
Methods Employing the stepwise glycosylation strategy, the target compounds were prepared via 10 steps of reactions using diosgenin as the starting material with an overall yield of 15%.
方法以薯蓣皂素为起始原料，采用逐步糖苷化策略，经10步反应制得目标化合物，总收率约为15%。
Methods Employing the stepwise glycosylation strategy, the target compounds were prepared via 10 steps of reactions using diosgenin as the starting material with an overall yield of 15%.
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