亚胺

Depending on the amine substitution, however, an enamine can be unstable with respect to its imine form.

根据对胺替代，不过，一enamine可以不稳定与尊重其亚胺形式。

In addition, the company marketing the world of high-quality insulating materials, such as the United States DuPont's polyester film, aromatic amines-washing paper, film-washing imine and composite products NMN, NHN and From the United Kingdom, South Korea, Japan, China's all kinds of insulation materials and industrial belt, I can according to customer's company, to provide the goods at the cutting and processing services.

此外，公司还经销世界各国的各种优质绝缘材料，如美国杜邦公司的聚酯薄膜，芳香聚洗胺纸，聚洗亚胺薄膜及复合产品NMN，NHN以及来自英国，韩国，日本，中国的各种绝缘材料和工业胶带等，同时我公司还可根据客户要求，提供上述货品的分切和加工服务。

It should be noted that the reaction with alkylimines failed to give the,β-lactam under current standard reaction conditions.

值得注意的是，在相同条件下，烷基亚胺参与的该反应都没能得到相应的β-内酰胺。

Low-valent titanium reagent induced the monomolecular reduction of N-substitutedphthalimides supplied a new method of synthesis hydroxyl lactams. This method was moreeconomic, convenient and in higher yields comparing with other methods reported before,therefore it has practical value.

4低价钛试剂引起邻苯二甲酰亚胺的单分子还原反应提供了一种合成羟基内酰胺的新方法，和文献方法相比，我们的方法试剂便宜易得，毋需溶剂，操作简便，收率也有所提高，具有实用价值。

A series of 3-naphthyl-2--1,3-thiazolidin-4-ones were synthesized by the three-component one-pot cyclocondensation of naphthylamine, aromatic aldehyde and 2-mercaptoacetic acid using a microwave-assisted method in the presence of DMAP/DCC.

利用微波促进的多组分一锅法，在封管条件下，以萘胺、芳醛和巯基乙酸为原料，4-二甲氨基吡啶/N，N'-二环已基碳二亚胺为催化剂，合成了系列新的噻唑烷酮衍生物，该反应具有时间短、操作简便等优点。

Mainly using protein - film voltammetric technique, we have achieved direct electrochemical response of lots of proteins such as hemoglobin, myoglobin, cytocrome c, cytocrome b5, horseradish peroxiase, GOD ,Vitreoscillia sp. haemoglobin, etc., at a series of protein membrane modified electrodes, for instance, protein/kieselgubr, protein/polyethylene glycol, protein/polyethyleneimine, protein/phosphatidylcholine, protein/DNA, protein/montmorillonite/polyvinyl alcohol, protein/silver nanoparticle/ cysteamine membrane modified electrode, etc., which are prepared by casting, incorperating or layer by layer self-assembly methods. Electrochemical behavior of these proteins in the films have been studied, and their structural and conformational changes have also been examined with spectrometric techniques.

三年来，在基金委的支持下，我们以蛋白膜伏安法这一新技术作为主要的研究手段，并结合其他生物、化学技术，研究了血红蛋白、肌红蛋白、细胞色素C、细胞色素b5、辣根过氧化物酶、葡萄糖氧化酶以及好氧革兰式阴性菌透明颤菌中的血红素类蛋白等多种蛋白质在以涂布和自组装方法制成的蛋白质/硅藻土膜、蛋白质/聚乙二醇膜、蛋白质/卵磷脂膜、蛋白质/聚乙烯亚胺膜、蛋白质/蒙托石/聚乙烯醇自组装膜以及蛋白质/银胶/半胱胺自组装膜等修饰电极上的直接电化学行为，结合各种光谱技术，对蛋白质在膜中的构象进行表征，探索其电子传递机理。

They were identified as 3-imino-N-(α-imidoethylamino)butyrolactam and neononane tetracid, respectively. The antitumoral activity on liver tumor cells SMMC-7721 was determined in vitro.

根据化合物的理化、谱学性质及X-射线晶体衍射分析结果，确定2个羧酸衍生物类化合物为3-亚胺基-N-丁内酰胺和新壬四酸。

The catalytic system composed of NHPI and transition metal ion can catalyze effectively ethane into acetic acid,cyclane into dicarboxylic acid,toluene into benzoic acid,alkene into epoxide,alkyne into acetylenic ketone,and amide into imide;NHPI used alone can catalyze adamantane to be carbonylated,hydrogen peroxide prepared by oxidization alcohol;NHPI combined with as...

NHPI与过渡金属离子组成的催化体系能高效地催化乙烷氧化为乙酸、环烷烃氧化为二元羧酸、甲苯氧化为苯甲酸、烯烃氧化为环氧化物、炔烃氧化为炔酮、酰胺氧化为酰亚胺；NHPI单独使用能催化金刚烷发生氧化羰基化反应、催化氧化醇制取过氧化氢；NHPI与有机助催化剂如偶氮二异丁腈、溴化季铵盐、蒽醌和醇等也能催化分子氧氧化反应。

Methods and Results— We synthesized the 3 components of a gene vector binding complex:(1) A poly allylamine bisphosphonate with latent thiol groups,(2) a poly ethyleneimine with pyridyldithio groups for amplification of attachment sites , and (3) a bifunctional (amine- and thiol-reactive) cross-linker with a labile ester bond.

方法和结果—我们综合了基因复合物载体的三种成分：(1)巯基聚丙烯胺二碳磷酸盐化合物，(2)能扩增结合位点聚乙烯亚胺-pyridyldithio复合物，(3)具有不稳定酯键的双功能交联剂。

In order to develop an useful synthestic process, we have synthesized amides with various substitutents. The isoquinoline skeleton was constructed through Bischler-Napieralski reaction, followed by asymmetric reduction of the imine intermediates with a Ru complex to form the only chiral center. Finally, we connected the two phenyl groups by Heck reaction and effectively obtained optically active aporphine alkaloids.

为了发展一套实用的合成方法，我们首先制备於苯环上具有不同种取代基的苯乙醯胺，接著透过Bischler-Napieralski反应进行分子内合环，并利用钌金属对亚胺中间体进行不对称的还原反应，建立出产物中唯一的光学活性中心，最后再利用Heck反应连结两个苯环，就可以顺利得到具有光学选择性的阿朴吩类天然物。

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。