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甲基麦角酰胺。Amine of acyl of ② methylic ergot.

乙酰基是酰基的一个例子。An example of the acyl group is the acetyl group.

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山西人善酿酷爱吃醋，素有“老醯儿”之称。Shanxi jealous love of good brew, known as "old acyl children, " said.

可与碱反应，可以发生酯化、酰卤化、酰胺化反应。With alkali reaction, can occur esterification, acyl halide, amide reaction.

以麦芽糖醇和脂肪酰氯为主要原料合成麦芽糖醇脂肪酸酯。Maltitol fatty acid ester was prepared with maltitol and fatty acyl chloride.

酰胺类除草剂是一种高效、高选择性的触杀性除草剂。Acyl Amino Herbicide is touch killing pesticide, which is mainly used to kill weed.

蒎酮酸经过酰氯化后再和二乙胺反应，合成了可能有生物活性的N，N-二乙基蒎酮酸酰胺。Pinonic acyl chloride was reacted with diethyl amine to synthesize N, N-diethyl-pinonic amide.

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察溶剂、酰基供体和加酶量对反应的影响，确定有机相中酶促拆分环氧丙醇的最适反应条件。The effects of organic solvents, acyl donors and amounts of lipase on the reaction were studied.

攷察溶剂、酰基供体和加酶量对反应的影响，确定有机相中酶促拆分环氧丙醇的最适反应条件。The effects of organic solvents, acyl donors and amounts of lipase on the reaction were studied.

详细研究利用生产己二酸副产的混合二元酸制取过氧化戌二酸的工艺流程和操作条件。Aim To synthesize O acyl or S acyl amino acids by condensation of dicarboxylic acids and amino acids.

这条路线是先用羧酸使噻吩已酰化制得酸基噻吩。The scheme initially involves acylation of thiophene using a carboxylic acid to afford the acyl thiophene.

该反应通过酯交换替换甘三酯中的酰基基团来改善油脂性质。This reaction provides a useful alternative for replacing the acyl group of glycerides to modify oil and fats.

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含1，3，4-噻二唑酰基硫脲和席夫碱类化合物的合成及生物活性研究。Studies on the Synthesis and Biological Activities of Acyl Thioureas and Schiff Bases with 1, 3, 4-thiadiazole.

微生物谷氨酰胺转胺酶，又称MTG酶，是一种催化酰基转移反应的转移酶。Microbial transglutaminase, also known as MTG enzyme, is an acyl transfer reaction catalyzed by the transferase.

制备酰基脲衍生物的方法，该酰基脲衍生物的盐，及其用作农药的用途。Method for producing acyl urea derivatives, salts of said acyl urea derivatives, and the use thereof as pesticides.

利用酯交换程度和酰基位移程度来评价各反应影响因素对反应工艺的影响。The ester exchange degree and degree of acyl migration were proposed to evaluate the effects on the reaction process.

红细胞的溶血磷脂酰胆碱则与游离的脂酸进行交换平衡。The choline of haemolysis phosphatide acyl of red blood cell undertakes commutative a balance with the fat acid of free.

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方法以5-氨基-2，4，6-三碘异酞酸为原料经酰氯化、酰胺化反应制得目标化合物。METHODS The title compound was synthesized from 5-amino-2,4, -6-triiodoisophthalic acid by acyl chlorination and amidation.

本研究为新型酰基硫脲类杀菌剂的开发研究提供了理论依据和研究方法。The research provides theoretical backgrounds and good quantum method for the further study of new acyl thiourea bactericides.

对分别使用酸酐和相应的游离羧酸作酰基给体时的反应性能进行了比较。The performance of the reaction using an acid anhydride as an acyl donor was compared with that using its corresponding free acid.