酮式烯酮

STUDIES ON PLANT PHOSPHOENOLPYRUVATE CARBOXYLASE——Ⅵ.

植物磷酸烯醇式两酮酸羧化酶的研究——Ⅵ。

The reaction of α-hydroxyketone with Michael acceptor nitroalkene.was studied. After many experiments, we then found that in the presence of Zn2 and cinchonine, the α-hydroxyketone could successfully react with nitroalkene. Under our optimized condition, we gained the 95% yield of product with the ratio of syn : anti of 3:1 and 72% ee value for syn-product.

有机碱作用下α－羟基酮对硝基烯烃的加成反应研究研究了α－羟基酮类化合物与Michael受体硝基烯烃类化合物的反应，通过分析和实验发现在Zn2和辛可宁的作用下α－羟基苯乙酮能够与硝基烯烃化合物顺利反应，在优化的条件下以95%产率和3：1的Dr主要得到顺式产物，其中顺式产物的ee值最高为72%。

The calculated results shed more light on the water′s influence on the proton transfer and offer a new insight into the structural tautomer interconversion of FM.

溶液状态下的质子转移研究将会对水分子对中心分子的异构化研究提供参考，同时也部分解释了试验中酮式比例高于烯醇式的现象。

The forming mechanism of dihydrophenophosphazine by the interaction of Ph〓NH and PCl〓 was studied, and the possible forming mechanism of spiro phosphonium chloride in the same reaction system was also proposed.

讨论了二苯胺与三氯化磷的成环机理以及反应过程中螺磷杂环化合物的形成机制，提出5，10-二氢磷杂吖嗪-10-氧化物存在类"烯醇—酮式"互变异构现象。

In this paper, the effects of different catalyst combinations on the synthesis of α-chloro-dodecanoic acid were investigated, in which a series of acyl chlorides such as 4-toluene sulfonyl chloride, dodecanoyl chloride, chlorosulphonic acid , etc.

本文从烯酮式反应机理出发，以α-氯代十二酸的合成为模型，对酰氯化试剂(对甲苯磺酰氯、十二酰氯、氯磺酸等)和质子酸催化剂(如H型离子交换树脂、氯磺酸、对甲苯磺酸、醋酸等)进行组合和选择，并与文献报道的特殊添加剂乙酐比较，研究不同催化体系在酸催化合成α-氯代脂肪酸时的催化作用。

In Granards' reactionof fluorinated β-ketophosphonium salts we found differentGranard reagents give different reaction mechanisms andPhMgBr realized the enolate reaction of fluorinatedβ-keto-phosphonium salts.

在研究含氟β-酮基鏻盐的β位亲核加成反应中，我们利用含氟α-烷氧基-β-酮基鏻盐与有机锂试剂的亲核加成反应一锅法高度立体选择性地合成了E式或Z式三氟甲基的烯醚类化合物。

Since many phenylvinyl ketone derivatives showed a certain anti- inflammatory activity, the indolyl group is introduced to this skeleton, and thus a series of 1, 4-penten-3-one derivatives characteristic of the structures of both phenylvinyl ketone and indole have been synthesized and characterized by elemental analyses, MS, UV-vis, and 〓 NMR as well. All these compounds are found to be trans-isomers.

考虑到苯乙烯酮类化合物的抗炎活性，本文将吲哚基团引入到该类化合物上，设计合成了一系列新的兼具苯乙烯酮和吲哚二者结构特征的1，4-戊二烯-3-酮衍生物Al-A24，并对其进行了表征，发现所有这些化合物均为反式构型。

Escherichia coli and many other microoganism synthesize aromatic amino acids through the condensation reaction between phospho enolpyruvate and erythro.

ppsA和tktA是芳香族氨基酸生物合成中心途径的两个关键酶基因，在大肠杆菌中，ppsA基因编码磷酸烯醇式丙酮酸合成酶A ，该酶催化丙酮酸合成磷酸烯醇式丙酮酸；tktA基因编码转酮酶A ，该酶在磷酸戊糖途径中生成 4 磷酸赤藓糖起主要作用。

L acted as tridentate ligand to chelate with metal atom in enol and ketone form respectively; In complex anion Co atom reside in tetrahedral coordination environment.

钴原子位于八面体配位环境中，配体L分别以烯醇式和酮式充当三齿配体与金属原子配位，配阴离子中Co原子位于四面体配位环境中。

In the fifth part, asymmetric synthesis of β,γ-trans-alkenyl α-amino esters was achieved by chiral phosphoric acid catalyzed transfer hydrogenation of β,γ-alkynyl α-imino esters. Utilizing Hantzsch ester as the hydrogen donor, both the alkyne and imine moieties of β,γ-alkynyl α-imino esters were reduced to yield β,γ-trans-alkenyl α-amino esters with up to 96% ee.

第五部分工作中，使用手性磷酸作为催化剂，Hantzsch酯作为氢源，β，γ-炔烃取代的α-酮酸酯亚胺中的炔键和亚胺官能团均被还原，以中等的收率和优秀的对映选择性（up to 96% ee）得到β，γ-反式烯烃取代的α-氨基酸衍生物。

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。