噁唑烷,oxazolidine英语短句,例句大全

噁唑烷,oxazolidine
1)oxazolidine[,?ks?'z?lidi:n]噁唑烷
1.Dimeric Catechin-oxazolidine Tannage and Histological Modality of Fore-and-aft Leather Shrinkage;二聚儿茶素-噁唑烷鞣法与革收缩前后的组织形态
2.Resorcin-oxazolidine Combination Tannage;间苯二酚与噁唑烷结合鞣法研究
3.THP-oxazolidine-fish Oil Tanning LeatherTHP盐-噁唑烷-鱼油鞣革工艺的研究

英文短句/例句

1.Synthesis and Antibacterial Activity of Bis-Oxazolidinones and 5-Substituted Ethyl Oxazolidinones;双噁唑烷酮和5-取代乙基噁唑烷酮类化合物的合成及其抗菌活性
2.Ternary Reaction of Resorcinol-oxazolidine-glycin间苯二酚-噁唑烷E-甘氨酸三元反应
3.Synthesis of a Novel Oxazolidine Tanning Agent and its Tanning Charactertics新型噁唑烷鞣剂的合成及其鞣性研究
4.THP-oxazolidine-fish Oil Tanning LeatherTHP盐-噁唑烷-鱼油鞣革工艺的研究
5.Study on the Synthesis and Herbicidal Activity of Substituted Phenyl Oxazolidone Derivatives;取代苯基噁唑烷酮类除草剂的合成及活性研究
6.Synthesis of (S)-(-)-5-(p-benzyloxybenzyl)-2,4-oxazolidinedione(S)-(-)-5-对苄氧基苄基-2,4-噁唑烷二酮的合成
7.Synthesis and Characterization of 3-Hydroxyethanyl-1,3-Oxazolidine and Its Initial Application3-羟乙基-1,3-噁唑烷的合成和表征及其初步应用
8.Synthesis and Antibacterial Activities of Novel Fluoroquinolone-Oxazolidinone Derivatives;新型氟喹诺酮—噁唑烷酮类化合物的合成及其抗菌活性研究
9.The Study on the Synthesis, Characteristition and Activity of Three Kinds of Herbicide Safeners of Dichloroacetyl Oxazolidine;三种潜在除草剂安全剂（二氯乙酰基噁唑烷）的合成、表征与活性研究
10.The Study on the Synthesis ,Characteristition and Activity of Herbicide Safeners of Dichloroacetyl Oxazolidine;噁唑烷类二氯乙酰基除草剂安全剂的合成、表征与活性研究
11.NMR Study on Oxazolidne Derivatives of 1,4:3,6-Dianhydro-D-Fructose基于1,4:3,6-二缩水-D-果糖的噁唑烷衍生物的NMR研究
12.Theoretical Studies on Catalytical Activity for the Chiral Oxazapholidine-Borane;手性噁唑磷烷—硼烷催化活性的理论研究
13.The Study of Asymmetric 1,3-Dipolar Cycloaddition Catalyzed by Chiral Oxazaborolidinone;手性噁唑硼烷酮催化1，3-偶极环加成反应的研究
14.Synthesis N-Perfluoroalkylethyl-substituted Oxadiazole, Triazole and Its Application of Quasiracemic Synthesis;氟碳烷基取代噁二唑、三唑的合成及在准外消旋合成中的应用
15.Synthesis of Diheterocyclic Compounds on 1,3,4-Oxadiazole-2-thiones and 1,2,4-Triazole-5-thiones氟碳烷基取代噁二唑、三唑的双杂环化合物的合成研究
16.Synthesis of Novel Chiral Cyclopropane-Based Bisoxazoline Ligands and Their Asymmetric Induction in Catalytic Asymmetric Reactions;环丙烷类双噁唑啉手性配体的合成及不对称诱导性能研究
17.Theoretical Studies on the Stereoselectivities in the Enantioselective Reductions of Prochiral Ketones Catalyzed by Oxazaborolidines;噁唑硼烷催化前手性酮不对称还原反应立体选择性的理论研究
18.The Asymmetric Catalytic Reduction of Prochiral Ketones Catalyzed by Chiral Oxazaborolidine;手性噁唑硼烷催化前手性酮的不对称催化还原反应

相关短句/例句

oxazolidinones噁唑烷酮
1.Synthesis and Antibacterial Activity of(S)-5-Acetamidomethyl-3-[(3-chloro-4-substituted aminomethyl)phenyl]-2-oxazolidinones;(S)-5-乙酰胺甲基-3-[(3-氯-4-取代胺甲基)苯基]-2-噁唑烷酮的合成及抗菌活性
2.Linezolid is a new class of oxazolidinones antibacterial agents that has been first used in clinical,it inhibits bacterial protein synthesis by blocking the formation of initiation complex.利奈唑胺(linezolid)是第一个应用于临床的新型噁唑烷酮类抗生素,通过抑制蛋白起始复合物的形成抑制细菌蛋白质合成,在体内、外对葡萄球菌、链球菌、肠球菌等耐药G+菌有广谱的抗菌作用,其临床疗效已经得到一系列Ⅲ期临床研究证明。
3.The oxazolidinones are a new class of totally synthetic antibacterials that inhibit protein synthesis via binding to a distinct region of 23S RNA of the 50S ribosomal subunit in prokaryotes.噁唑烷酮类抗菌剂是一类新型的全合成抗菌药物，作用于细菌蛋白质合成的早期阶段(主要作用靶点是核糖体50S亚基的23S rRNA)，表现出高度的抗耐药性革兰氏阳性菌活性，其代表药物吗啉噁酮(linezolid)已上市。
3)oxazolidinone噁唑烷酮
1.Analysis of (4S)-4-benzyl-3-(2′(E)-butenyl)-2-oxazolidinone by nuclear magnetic resonance;(4S)-4-苄基-3-(2’(E)-丁烯酰基)-2-噁唑烷酮的核磁分析
2.Studies on synthesis of NCPS supported oxazolidinone chiral auxiliary;线型聚苯乙烯支载噁唑烷酮手性助剂的合成研究
3.Preparation of (S)-(+)-4-Phenyl-2-oxazolidinone;手性4-苯基-2-噁唑烷酮的合成研究
4)oxazaphospholidine噁唑磷烷
1.Density functional (BHandH) calculations, using 6-31G** basis set, have been employed to study the reaction mechanism of the enantioselectivity in a chiral 1,3,2-oxazaphospholidine-borane cata- lyzed reduction of acetophenone.应用密度泛函理论BHandH/6-31G**计算方法研究新型手性非金属催化剂1,3,2-噁唑磷烷-硼烷催化还原苯乙酮的对映选择性反应机理,确定了在反应途径上的反应物、络合物、过渡态,中间体和对映体中间产物。
5)oxazaborolidine噁唑硼烷
1.The asymmetric reduction of ketosulfone with borane catalyzed by oxazaborolidine is computed by means of the semi-empirical MNDO method.对噁唑硼烷催化前手性酮砜不对称还原反应进行了半经验MNDO研究。
2.Asymmetric reduction of prochiral ketones using oxazaborolidines has become one of the standard tools for the synthetic chemist, allowing access to enantiomerically enriched secondary alcohols with excellent enantiomeric excess that may seve as the chiral ligands for enantionselectivity synthesis and highly useful intermediates in the sy.手性噁唑硼烷催化前手性酮的不对称还原反应已成为合成化学家的重要手段之一,这种方法获得的手性仲醇具有较高的ee 值,它们可作为不对称合成中的手性配体及活性物质、天然产物和药物的手性中间体。
6)isoxazolidine异噁唑烷