目的考察3-（4-碘苯甲酰基）丙酸的最佳合成条件。
Objective To determine the best synthesis condition of 3-(4-iodobenzyl)propionic acid.
邻位-取代的苯甲酰基胍，其制备方法，作为药物或诊断剂的应用及含它们的药物。
Ortho-substd. benzoyl guanidines, their preparing process and use as medicine and diagnostic reagent, and medicine contg. same.
对苯甲酰基脲类几丁质合成抑制剂的结构、合成方法、作用机制、代谢及环境安全性等进行了评述。
The structures, synthetic methods, insectical mechanism, degradation, together with environmental safety of benzoyl urea chitin synthesis inhibitors were reviewed in this paper.
脱苯甲酰基方法在此粗分为四类，即酸催化水解法、碱催化水解法、选择性脱苯甲酰基法和其它特殊方法。
The methods are divided into four kinds: acid catalytic hydrolysis, alkali catalytic hydrolysis, selective debenzoylation and special methods.
通过苯甲酰基修饰的苯乙烯-二乙烯苯吸附树脂ZH-02对水中腐殖酸和苯酚进行了单组分和双组分的静态吸附。
The static adsorption of humic acid and phenol from water in single and double component system onto ZH-02 resin of styrene-divinylbenzene modified by benzoyl group was carried out.
本课题以二茂铁为原料，与邻甲氧基苯甲酰氯反应生成邻甲氧基苯甲酰基二茂铁，再与一系列胺反应合成亚胺，最终还原为二茂铁氨基化合物。
The title compounds were obtained by the reduction of the corresponding ferrocenyl imines, which were prepared from ferrocene and o-anisic acid chloride, followed by amination with aromatic amines.
结果：从广枣70 %乙醇提取物中分离出一个胸腺嘧啶脱氧尿苷类化合物，结构为5-甲基-3′ ，5′-二氧-（对氯苯甲酰基）-2′-脱氧尿苷。
RESULT: A deoxyuridine was isolated from 70% alcohol extract and identified as as 5-methyl-3′, 5′-di-O-(p-chlorobenzoyl)-2′-deoxyuridine.
结果：从广枣70 %乙醇提取物中分离出一个胸腺嘧啶脱氧尿苷类化合物，结构为5-甲基-3′ ，5′-二氧-（对氯苯甲酰基）-2′-脱氧尿苷。
RESULT: A deoxyuridine was isolated from 70% alcohol extract and identified as as 5-methyl-3′, 5′-di-O-(p-chlorobenzoyl)-2′-deoxyuridine.
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