联菲双恶唑啉还可以用于催化其他的反应。
前言：目的：提高磺胺甲恶唑的体外溶出速率。
Objective: To improve the dissolution of the sulfamethoxazole invitro.
而且和苯环衍生的硫恶唑啉相比反应活性相对较高。
In addition, these ligands showed higher activity than thioether deveritives of phenyl oxazolines.
为菌源，研究了这两种混合菌降解精恶唑禾草灵的效果。
The paper studied the impact of two mixed culture on the degradation of Fenoxaprop-p-ethyl, which are from Alcaligenes sp.
综述了近年来恶唑烷酮类和喹诺酮类抗菌药物的研究进展。
This paper reviews advances in the research of the antibacterials of oxazolidinones and quinolones.
本文针对含恶唑环耐高温聚酰亚胺的合成与性能进行了研究。
The synthesis and performances of PI including oxazole were studied in this term.
目的：对复方磺胺甲恶唑片中甲氧苄啶的鉴别方法进行改进。
Object: To improve the identification method for trimethoprim of compound sulfamethoxazole tablets.
手性双恶唑啉是在不对称催化中广泛应用的一类重要的配体。
Chiral bisoxazolines have been widely applied ligands to asymmetric catalysis and a series of optically active bisoxazolines with rigid backbones and different chelate sizes were synthesized.
对2 -芳基苯并恶唑衍生物的光谱及光物理行为进行了研究。
The spectra and photophysics of 2-aryl-benzoxazole derivatives have been studied in this work.
异恶唑杂环化合物在专利报道中出现许多高效或超高效的新品种。
Many isoxazole heterocycle compounds have efficiency or super-efficiency in controlling the growth of weeds.
前言：目的：对两批掺假复方磺胺甲口恶唑片进行全面质量分析。
Objective: This study evaluated the quality of the two batches of Compound Sulfamethoxazole Tablets.
介绍了一种新型高性能有机纤维聚对苯撑苯并双恶唑简称PBO。
Polyp-phenylene benzobisthiazole(PBO), a new high-performance organic fiber, is introduced in this paper.
目的研究康复新对恶唑酮诱导的小鼠实验性肠炎的影响，并探讨其机制。
AIM To investigate the effect and mechanisms of Kangfuxin on oxazolone induced colitis in mice.
为何甲氧苄啶含量测定时供试液的稀释倍数与磺胺甲恶唑测定时的要不同？
Why is the more diluted solution used for the assay of trimethoprim than that for sulfamethoxazole?
本文是关于新型抗菌剂恶唑烷酮类化合物的设计、合成及其抗菌活性的研究。
The design, synthesis and antibacterial activity of new oxazolidinone derivatives was studied in this paper.
对于按照抗生素不同进行分析，应用阿莫西林和磺胺甲基异恶唑同样没有显著差异。
When data were categorized based on antibiotics used, which included amoxicillin and cotrimoxazole, the differences remained nonsignificant.
目的研究光纤药物溶出度实时测定(FODT)仪监测复方磺胺甲恶唑片的溶出度。
OBJECTIVE To determine the dissolution rate of compound sulfamethoxazole tablets with the instrument of fiber-optic in situ dissolution testing (FODT).
分离菌株对青霉素、磺胺甲基异恶唑具抗药性，对氨苄青霉素、环丙沙星、头孢曲松钠高敏。
The isolates were resistant to penicillin G and sulfamethoxazole, and highly sensitive to ampicillin, ciprofloxacin and ceftriazone.
结果表明，用本文所述自由基悬浮聚合或本体聚合方法都能合成含恶唑啉环的活性聚苯乙烯。
The results showed reactive PS containing oxazoline ring could be synthesized by the suspension polymerization and bulk polymerization mentioned in this paper.
以邻氨基苯酚和尿素为原料生成苯并恶唑酮，再用过氧化氢盐酸氯化制得6-氯苯并唑酮。
Benzoxazolone was prepared from o-aminophenol and urea and then was chloridized by hydrogen peroxide and hydrochloric acid to get 6-chlorobenzoxazolone.
综述了恶唑菌酮的环境行为以及在生物体中的残留毒性的研究进展，并提出了今后的研究重点。
The study progress on environmental activities and residue toxicology of famoxadone were described, and the research emphasis in the future was put forward.
本发明属于农用杀菌剂的技术领域，具体涉及一种恶唑菌酮和保护性杀菌剂复配的组合物及应用。
The invention belongs to the technical field of agricultural fungicide, and in particular relates to a composition with famoxadone compounded with protective fungicide, and application thereof.
Joseph Pernerstorfer： 取代的恶唑烷酮和其在血液凝固领域中的应用。
Substituted oxazolidinones and their use in the field of blood coagulation.
本文综述了手性双恶唑啉的合成及其金属配合物作为手性催化剂在催化不对称反应中的应用研究进展。
The synthesis and applications in catalytic asymmetric synthesis of C2-symmetric chiral bis (oxazoline) and its metal complexes are reviewed in this article.
以L—丝氨酸为原料，合成了旋光纯度很高的4（S）—2—甲基—4—甲氧羰基—2—恶唑啉单体。
A new optically active monomer of 4(S)—2—Methyl—4—Methoxycarbony1—2—Oxazoline has been synthesized from L—serine.
概括了近年来C_2轴手性双恶唑啉试剂及其金属络合物的合成及在催化不对称合成应用上的研究进展。
This review describes recent advances in the synthesis of C_2-symmetric chiral bis (oxazoline) ligands and the utility of its metal complexes in the catalysis of asymmetric syn - thesis.
作为色谱固定相，磺胺甲恶唑烙印聚合物和目标分子之间的相互作用除氢键作用外，也存在着疏水作用。
The interaction between the MIP and target molecules were found to arise from hydrogen bonding in the imprinted area and the hydrophobic interaction in the non-imprinted area .
作为色谱固定相，磺胺甲恶唑烙印聚合物和目标分子之间的相互作用除氢键作用外，也存在着疏水作用。
The interaction between the MIP and target molecules were found to arise from hydrogen bonding in the imprinted area and the hydrophobic interaction in the non-imprinted area .
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