羰基的

After hydrogenation of the double bond and the addition of alkyne to a carbonyl we introduced the N-hydroxy group by SN2 reaction.

不对称氢化和炔负离子对羰基的立体选择性加成构建了两个新的手性中心，之后用羟胺衍生物对羟基的SN2取代反应引入了羟胺片断。

Methylcarbonate is an important organic industrial intermediate. Because its molecular structure contains carbonyl, methyl, methoxyl group and carbonyl methoxyl group, etc., it can be used in carbonylate, methylate, methoxylate organic synthetic reaction.

碳酸二甲酯是一种重要的有机化工中间体，由于其分子结构中含有羰基、甲基、甲氧基和羰基甲氧基，因而可广泛用于羰基化、甲基化、甲氧基化和羰基甲基化等有机合成反应。

The compounds are represented by the structural Formula 1, Chemical formula should be inderted here as it appears on the abstract in paper form. a prodrug thereof, or any pharmaceutically acceptable salt, solvate, isomer or racemic mixture of the compound or said prodrug wherein R1 is heteroaryl, N-arylaminocarbonyl, N-heteroarylaminocarbonyl, benzimidazolyl or benzothiazolyl; R15 is present or not and if present is H, aryl, alkyl, arylalky or heteroarylalkyl; A is aryl, heteroaryl, cycloalkyl, cycloalkylidene, heterocycloalkylidene or heterocycloalkyl wherein said aryl, heteroaryl, cycloalkyl, cycloalkylidene, heterocycloalkylidene and heterocycloalkyl moieties may be substituted or unsubstituted; and B, L, X and R18 are defined herein.

所述化合物用结构式1表示，包括其前药或所述化合物或所述前药的任何药学上可接受的盐、溶剂合物、异构体或外消旋混合物，其中R 1 为杂芳基、N-芳基氨基羰基、N-杂芳基氨基羰基、苯并咪唑基或苯并噻唑基；R 15 存在或不存在，如果存在，则为H、芳基、烷基、芳基烷基或杂芳基烷基；A为芳基、杂芳基、环烷基、环烷叉基、杂环烷叉基或杂环烷基，其中所述芳基、杂芳基、环烷基、环烷叉基、杂环烷叉基和杂环烷基部分可被取代或未被取代；B、L、X和R 18 如说明书所定义。

Chapter three: The studies of zinc dust assisted the green carbonyl olefination under thesolvent-free conditions.

第三章：锌粉促进无溶剂下羰基化合物的绿色烯基化反应研究该部分首次研究了在TMSiCl存在下，无溶剂非催化条件下，锌粉促进溴化苄与羰基化合物的烯基化反应，发现在无溶剂锌粉促进下，可以将羰基化合物立体选择性

In this thesis, investigations focused on heteropoly acids-catalyzed C-C and C-N bond formation reactions and the synthesis of xanthenediones and acridinediones under thermal conditions are described.1.12-Phosphotungstic acid has been used as an efficient,eco-friendly,and air- and moisture-stable catalyst to promote the direct dehydrative substitution of the hydroxy group of benzylic and allylic alcohols with variousβ-dicarbonyl compounds.

本篇论文主要描述了杂多酸催化下的C-C和C-N键的生成，以及无溶剂直接加热下合成十氢氧杂蒽二酮和9-芳基十氢吖啶二酮。主要内容如下：1。在磷钨酸催化下，1，3-二羰基化合物与醇能够顺利偶合，脱除一分子的水，生成烷基化的1，3-二羰基化合物。反应在甲苯中进行时，二芳基甲醇能与各类1，3-二羰基化合物反应，成率很高；但对于1-苯乙醇，只能得到很低的产率。

The recombinant proteins were purified according to the protocol of Ni-NTA Agarose and detected by SDS-PAGE, and TLC. Western blotting was used to identify their immunoreactivities with the serum of patient with clonorchiasis.

寄生性蠕虫以胞质GSTs为主，参与对由虫体代谢和宿主免疫系统所产生的脂质过氧化物和细胞毒性的羰基的解毒，对虫体的生存起重要的作用，是免疫疗法、化学疗法和免疫诊断潜在的靶标。

The dissertation mainly consists of two parts:1. The Reaction Chemistry of Alkynes under Palladium Catalysis Part 1 studies the reaction α,β-unsaturated carbonyl compounds with alkenylpalladium intermediate generated by nucleopalladation, and discovered 1 the Pd-catalyzed tandem addition reaction of halides, alkynes and α,β-unsaturated carbonyls,2 the four-component tandem addition reaction of halides, alkynes and α,β-unsaturated carbonyls, 3 the tandem intramolecular oxypalladation-conjugate additionreaction of alkynoic acids with α,β-enals. These new reactions provide notonly efficient highly stereoselective methods for the synthesis of γ,δ-unsaturated,polyunsaturated carbonyl compounds and γ-lactonic aldehydes, but also thebasic transformations for a number of C-C bond formation reactions which can be usedto design synthesis of many acyclic, cyclic or polycyclic compounds.

本论文的主要工作分为两个部分：一、钯催化下炔烃的反应化学在本小组前人工作的基础上，我们详细研究了炔烃亲核钯化产生的烯基钯中间体与α，β-不饱和羰基化合物的反应，发现两价钯催化下卤离子-炔烃-α，β-不饱和醛酮的串联加成反应、卤离子-炔烃-α，β-不饱和醛酮的西组分串联加成及炔酸分子内氧钯化-串联Michael型加成反应；由此发展了γ，δ-不饱和醛酮、多不饱和羰基化合物和带有醛酮基侧链的γ-丁内酯衍生物的高立体选择性合成方法，这一过量卤离子存在下的烯基钯对α，β-不饱和羰基化合物共轭加成反应的发现，为大量碳-碳键形成反应的实现提供了基础，使我们能够从这一基本反应出发，设计和开发多种分子内、分子间的碳碳成键反应，以好的立体、区域选择性组建开链、环状及多环类型的化合物。

Photolysis of paramethyl benzyl manganese pentacarbonyl5Mn-p-CH2C6H4CH3 (4a)and paramethoxy benzyl manganese pentacarbonyl5Mn-p-CH2C6H4OCH3(4b) with 1-2 equivalents of R3SiH in C6H6 or C6D6 at 5℃ yields the silyl manganese pentacarbonyls5MnSiR3 [SiR3 = SiMe2Ph (1b), SiMePh2 (1c), SiPh3 (1d), SiHPh2 (1e), SiEt3 (1f), SiMe2tBu(1g), and SiMe2Et (1h) ] in moderate to high yields after chromatographic purification.

对甲基卞基五羰基锰5Mn-p-CH2C6H4CH3（4a）或对甲氧基五羰基锰5Mn-p-CH2C6H4OCH3（4b）与1-2当量R3SiH的C6H6 或C6D6溶液在5oC光解，经色谱纯化后得到中等或高收率硅烷基五羰基锰5MnSiR3［SiR3 = SiMe2Ph（1b），SiMePh2（1c），SiPh3（1d），SiHPh2（1e），SiEt3（1f），SiMe2tBu（1g），和SiMe2Et（1h）］。

The recent research progress of oxidation carbonylation of amines/β-amino alcohols, alkoxycarbonylation of epoxides, carbonylative Suzuki coupling, carbonylative Sonogashira, and double carbonylation of aryl iodides has been presented, focusing on the carbonylation reactions studied by us in the past few years, with 81 references.

综述了胺／氨基醇类化合物氧化羰化、环氧化合物氢酯基化、碘代芳烃的羰化Suzuki偶联、羰化Sonogashira以及双羰基化等重要羰基化反应的研究状况，特别是结合本课题组近年来在该领域中的工作，并对羰基化反应的发展及应用前景进行了展望。

The positive peptide cleavage promoted by complex, CuⅡL and the negative response of CuⅡ/dien complex suggest the merely hydroxy pendant in complex have no ability to attack the peptide bond. The synergic carbonyl activation by metal coordination is essential for the cleavage of peptide bond promoted by CuⅡL.

比较相应铜配合物及二乙烯三胺铜配合物的切割性能，提示羟乙基侧臂单独难以实现相邻肽键的切割，高配位数金属中心对肽键羰基的活化与羟基的协同进攻是该类配合物切割多肽的可能机制。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。