酰亚胺

Part 2. Annulation reaction of 3, 4-dichlorocoumarin (1) and 3, 4-dichloromaleimide (8) by a new general annulation strategy developed in this group with 2-phenylbenzofuran (15), 3-phenylbenzofuran (16), 2, 5-diphenyloxazole (17), 2, 5-diphenylthiazole (18), 2-methyl-4-phenylthiazole (19) and 2, 3-dimethoxy-1, 3-butadiene (40) were investigated.

二。在本课题组前一阶段提出的从二氯代环烯酮与1，1-二芳基乙烯的光化反应以及光化反应中得到的环丁烷产物的连续电环化反应对3，4-二氯马来酰亚胺以及3，4-二氯香豆素进行增环反应的工作基础上，研究了3，4-二氯香豆素（1）和3，4-二氯马来酰亚胺（8）与5个α-苯基取代的环烯烃2-苯基苯并呋喃（15），3-苯基苯并呋喃（16），2，5-二苯基噁唑（17），2，5-二苯基噻唑（18），2-甲基-4-苯基噻唑（19），以及一个丁二烯——2，3-二甲氧基丁二烯（40）进行的芳香族增环反应。

A series of diazonium salts of 4-(N-methyl-N-phenylamino)-3-amino-1,8-naphthalic anhydride 5a, its naphthalimide derivative 5b, and 5e were designed and synthesized,and it was the first time to discover that aromatic radical-induced intramolecular aromatic 1, 5-hydrogen transfer was also involved in the nitrogen-contianed system during Pschorr cyclization.

实验设计合成了4--3-氨基-1，8-萘酐的重氮盐5a、其衍生物N-丁基-4--3-氨基-1，8-萘酰亚胺的重氮盐5b和N--4--3-氨基-1，8-萘酰亚胺的重氮盐5c，并首次发现了通过普朔尔环化反应以氮甲基化的氮为桥原子的体系存在着芳香自由基诱导的芳香1，5-氢转移。

2 New carbonyl functionalized imide derivatives of maleimide were synthesized by the direct reaction of amino acids with maleic anhydride.

用氨基酸与苹果酸酐直接反应，合成了两个含羧基官能团的苹果酰亚胺，为氨基酸氮端的保护以及含羧基官能团的酰亚胺类化合物的合成提供了一种直接、简便的新方法。

In order to obtained the six-membered ring compound and a thorough assignment of the spectra, and further to prove that the six-membered ring compound was formed from the hydrogen transfer, the compound N-butyl-4-(N-methylphenylamino)-5-amino- 1, 8-naphthalimide 6 was designed to obtained with N-butyl-4-bromo-5-amino-1, 8-naphthalimide and N-methyl phenylamine as the starting material. However it was difficult to obtain the desired product as the different solvent giving the different products except the desired product.

为了能够得到六元环化合物作为定标的物质及其确切的谱图分析结果，并且为了进一步证明由五元环产物通过氢转移得到六元环产物的正确性，设计用N-丁基4-溴-5-氨基-1，8-萘酰亚胺与N-甲基苯胺反应生成N-丁基-4--5-氨基-1，8-萘酰亚胺6，结果发现这种方法很难实现，选择不同的溶剂会生成不同的产物，却都不是目标产物。

A series of angular thiazonaphthalimides was designed and synthesized by fusing a thiazole ring to the naphthalimide skeleton.

通过在萘酰亚胺母体上并入噻唑杂环，设计并合成了一系列新型的具有角型结构的萘酰亚胺类化合物。

The synthetic progress of polysuccinimide using maleic acid as original material was studied by two steps of aminization and polymerization. Changes of reactant and product composition in aminization reaction step was studied by using bromine value analysis method. It was found that amine salt and amide were main products in this step.

对以马来酐为原料合成聚琥珀酰亚胺的两个反应过程进行了研究，通过溴价测定法研究了胺化反应阶段反应物及产物各组分的变化情况，确定胺化反应阶段的产物组分主要是胺盐和酰胺。

Two kinds of polyaspartic acid derivates, i.e. PEG-g-PAsp and PEG-g-PDEA, were prepared through the ring-opening reaction of polysuccinimide by CH3O-PEG-NH2, followed by alkaline hydrolysis and aminolysis, respectively.

通过胺端基聚乙二醇(CH3O-PEG-NH2)开环聚琥珀酰亚胺，进一步碱解和胺解制备了聚乙二醇接枝聚天冬氨酸和聚乙二醇接枝聚乙二胺基天冬酰胺两种聚天冬氨酸衍生物。

Was synthesized from succimide by bromination with bromine,methylation with dimethyl sulfate and the reaction of indolyl magnesium bromide with 2,3-dibromoN-methylmaleimide.

以琥珀酰亚胺为起始原料，经过溴化、甲基化后再与吲哚溴化镁加成反应合成了2-溴-3-(1H-吲哚-3)-N-甲基马来酰亚胺，总收率44.8%，其结构经1H NMR和IR确证。

DSC curve revealed two curing peaks,of which one at around 150℃ was attributed to the condensation reaction of methylol groups formed in minor quantities on the phenyl rings,and the other at around 250℃ was attributed to the addition curing reaction of the maleimide groups.

利用DSC和TGA研究了 N -苯基马来酰亚胺改性酚醛树脂的固化特性和耐热性能，发现PPMF树脂经历了两个固化阶段，第一阶段是少量羟甲基的缩合，第二阶段为马来酰亚胺的双键打开自交联形成。

The method is presented as follows: firstly, potassium phthalimide is synthesized by phthalimide reacting with potassium hydroxide at the room temperature.

该法先在室温条件下以邻苯二甲酰亚胺与氢氧化钾反应合成了邻苯二甲酰亚胺钾。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。