噁唑烷二酮,oxazolidinedione
1)oxazolidinedione噁唑烷二酮
1.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
英文短句/例句

1.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
2.Theoretical Study on Reaction Mechanism in Oxazaborolidine-Catalyzed Reductions of Diphenyl Diketohexane;噁唑硼烷催化还原二苯基已二酮的反应机理研究
3.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
4.Ternary Reaction of Resorcinol-oxazolidine-glycin间苯二酚-噁唑烷E-甘氨酸三元反应
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.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
7.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
8.Synthesis and Characterization of 1,3,4-Oxadiazole-2-thione Derivatives联苯取代1,3,4-噁二唑-2-硫酮的合成与表征
9.Synthesis of 2-Aryl-5-(6-pyridazinon-3-yl)-1,3,4-oxadiazoles2-芳基-5-(6-哒嗪酮-3-基)-1,3,4-噁二唑的合成
10.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
11.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
12.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
13.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
14.Protective effect of thiazolidinediones on the kidney噻唑烷二酮类药物对肾脏的保护作用
15.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
16.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
17.Synthesis and Biological Activity of Multi-perfluoroalkyl-substituted and Diphenyl-substituted Oxadiazole Derivatives多氟烷基和联苯取代噁二唑类的合成及活性研究
18.SYNTHESIS AND PHOTOPHYSICAL PROPERTIES OF CONJUGATED POLY(9,9-DIALKYLFLUORENOLBENZOBISOXAZOLE)S含烷基侧链聚芴基苯并二噁唑聚合物的合成及性能研究
相关短句/例句

2,5-oxazolidinedione2,5-噁唑烷二酮
3)2,4-oxazolidinedione2,4-噁唑烷二酮
1.Synthesis and Determination of Absolute Configuration of (R)-(+)-5-{4-[2-(5-Chloroindazol-2-yl)ethoxy]benzyl}-5-methyl-2,4-oxazolidinedione(R)-(+)-5-甲基-5-{4-[2-(2-(5-氯吲唑基))乙氧基]苄基}-2,4-噁唑烷二酮的合成及其绝对构型的确定
4)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。
5)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
6)Propazone5,5-二甲基噁唑烷-2,4-二酮
延伸阅读

噁唑分子式:暂无分子量:暂无CAS号:288-42-6性质:暂无制备方法:暂无用途:暂无